Normal physiological processes, including oxidative stress, neuronal activation, and gene transcription, can damage DNA in neurons1,2,3,4. If not precisely repaired, DNA damage creates permanent lesions in the neuronal genome, referred to as somatic mutations. Recent single-cell sequencing studies report that every neuron in the mammalian brain may contain unique somatic mutations5,6,7.

DNA mutations are more abundant in individuals with neurodegenerative disorders8,9,10,11,12, and reviewed in ref. 13. In fact, one common phenotype across numerous neurodegenerative disorders, including Alzheimer’s disease (AD), Parkinson’s disease (PD), amyotrophic lateral sclerosis, and ataxia-telangiectasia, is an abnormal accumulation of DNA damage in neurons13,14,15,16. DNA damage-induced neurodegeneration is frequently associated with hyperactivation of the nicotinamide adenine dinucleotide (NAD+) consuming enzyme PARP1 (poly(ADP-ribose) polymerase 1), which leads to energetic breakdown and cell death17,18,19,20. A greater understanding of the genes and the molecular mechanisms that maintain genomic integrity in postmitotic neurons could thus have therapeutic relevance for multiple neurodegenerative diseases.

Decades of research in yeast and mitotic mammalian cells support a role for topoisomerase 1 (TOP1) in gene transcription and maintenance of genomic integrity21,22. Recent studies suggest that transcriptional stress-driven DNA damage is also prevalent in postmitotic neurons and has the potential to disrupt genes that neurons depend on most2. We recently identified TOP1 as a key transcriptional regulator in postmitotic neurons23,24. TOP1 relieves DNA supercoiling generated during transcription by catalyzing a single-strand DNA cleavage22. During this reaction, TOP1 transiently binds to the DNA forming a cleavage complex (TOP1cc). Acute depletion of TOP1 or acute treatment with topotecan, a TOP1 inhibitor, resulted in the downregulation of long genes (>100 kb) in cultured cortical neurons23. TOP1cc-dependent and -independent mechanisms were implicated in these transcriptional responses24. Long genes, as a class, are disproportionately associated with neuronal functions23,25, and acute inhibition of TOP1 impaired long genes associated with synaptic function in neuronal cultures26. Using a single-cell RNA-sequencing (RNA-seq) approach, we also found that excitatory neurons in lower cortical layers expressed long genes to a greater extent when compared to excitatory neurons in upper cortical layers in embryonic and early postnatal mice27.

Based on these observations, we hypothesized that TOP1 might maintain genomic integrity and/or maintain transcriptional output in the central nervous system and that deletion of Top1 would have the greatest impact on lower layer excitatory cortical neurons. Here, we tested this hypothesis by conditionally deleting Top1 in postmitotic excitatory neurons in the mouse cerebral cortex and hippocampus.


Top1 cKO mice show motor deficits and early death

To study the requirement for TOP1 in postmitotic excitatory neurons of the cerebral cortex and hippocampus, we crossed Top1 conditional knockout mice (Top1fl/fl)24 with the Neurod6Cre mouse line28. Neurod6 expression begins at embryonic day 11.5 and is maintained throughout maturation in postmitotic excitatory neurons of the mouse cerebral cortex and hippocampus, except for the dentate gyrus (DG), where Neurod6 is only transiently expressed postnatally28. Both homozygous Top1-knockout mice (Neurod6Cre/+::Top1fl/fl, referred to as Top1 cKO) and heterozygous (HET) Top1 KO mice (Neurod6Cre/+::Top1fl/+, referred to as Top1 cHET) were generated. Neurod6+/+::Top1fl/fl or Top1fl/+ mice were used as a control (wild-type (WT)). To confirm Top1 deletion, we examined TOP1 protein levels at postnatal day 0 (P0) through immunostaining. TOP1 was ubiquitously expressed in WT and Top1 cHET cortex and hippocampus (Fig. 1a, Supplementary Fig. 1), but was absent in most cortical and hippocampal NEUN+ neurons of Top1 cKO mice (Fig. 1a, Supplementary Fig. 1). Cortical neurons that stained positive for TOP1 in Top1 cKO mice are most likely interneurons, which do not express Neurod6. Likewise, most of the neurons in the DG stained positive for TOP1 at this time point (Fig. 1a, Supplementary Fig. 1), consistent with transient postnatal Neurod6 expression in DG neurons.

Fig. 1: Deletion of Top1 in cortical and hippocampal neurons impairs motor function and causes premature death.
figure 1

a TOP1 and (inset) NEUN immunostaining of P0 WT and Top1 cKO somatosensory cortex (Ctx) and hippocampus (Hip). Scale bar = 300 μm, inset scale bar = 50 μm. Images are representative of two independent experiments. b Body weight of Top1 WT cHET and cKO mice at different time points. WT: P0 n = 10, P7 n = 41, P15 n = 37; cHET: P0 n = 6, P7 n = 27, P15 n = 20; cKO: P0 n = 6, P7 n = 17, P15 n = 12. n.s.p > 0.05, ****p < 0.0001. WT vs. cHET p values were not significant in all comparisons. One-way ANOVA with Dunnett’s multiple comparison test for each time point. c Kaplan–Meier survival curve. Mantel–Cox test. WT vs. cHET p > 0.05. n = 24 mice per genotype. d Righting and geotaxis assays performed on P7 (WT = 13, cHET = 13, cKO = 13 mice) and P12 mice (WT = 10, cHET = 10, cKO = 9 mice). WT vs. cHET p values were not significant (p < 0.05). One-way ANOVA with Dunnett’s multiple comparison test. Dashed lines represent cutoff time. Values are mean and error bars are ±SEM.

The body weights of Top1 cKO mice were comparable to WT mice at birth, but increased to a lesser extent at P7 and P15 (Fig. 1b). Top1 cKO were viable up to the second and third postnatal week (Fig. 1c). Top1 cKO mice also showed a severe motor deficit as assessed by the righting reflex assay at P7 and the geotaxis assay at P12 (Fig. 1d). No differences in body weight, viability, or motor function were observed in Top1 cHET compared to WT mice (Fig. 1b–d). These data indicate that deletion of Top1 in postmitotic excitatory cortical and hippocampal neurons did not overtly affect brain or body development up to birth, but impaired motor function and caused premature death within the first month of life.

Top1 cKO mice show early-onset neurodegeneration

To determine if Top1 deletion affected postnatal brain size, we quantified brain weight in WT, Top1 cHET, and Top1 cKO mice at different time points. Relative to P0, WT brain weight was 2.5-fold greater at P7 and 3.5-fold greater at P15 (110.3 ± 0.003 mg at P0, 274.9 ± 0.008 mg at P7, and 381.6 ± 0.008 mg at P15) (Fig. 2a). Top1 cKO brain weights were comparable to WT at P0, increased ~2-fold by P7, but then failed to increase at later ages (Fig. 2a), and were visibly smaller than WT brains (Fig. 2b) (101.6 ± 0.001 mg at P0, 200.2 ± 0.008 mg at P7, and 200.6 ± 0.014 mg at P15). Top1 cHET brains were comparable to WT at all time points (106.0 ± 0.002 mg at P0, 263.6 ± 0.007 mg at P7, and 365.4 ± 0 mg at P15).

Fig. 2: Brain, cerebral cortex, and hippocampus size reduced in Top1 cKO mice.
figure 2

a Brain weight quantification of WT (P0 n = 11, P7 n = 22, P12 n = 8, P15, n = 13), cHET (P0 n = 14, P7 n = 12, P12 n = 4, P15 n = 1) and Top1 cKO mice (P0 n = 17, P7 n = 14, P12 n = 3, P15 n = 10). Values are mean and error bars are ±SEM. n.s.p > 0.05, ****p < 0.0001. WT vs. cHET p values were >0.05 in all comparisons. One-way ANOVA with Dunnett’s multiple comparison test. b Representative images of P15 brains. Scale bar = 0.5 cm. c Sections containing the cerebral cortex and hippocampus immunostained for CUX1, CTIP2, and NEUN to identify layer 2–4, layer 5 and 6 neurons, and all neurons, respectively. Dashed lines delineate cortex, hippocampus, and cortical layers (inset). Scale bar = 300 μm, inset scale bar = 200 μm. Images are representative of three independent experiments. n.s. not significant.

To determine if the cortex and hippocampus were affected, we immunostained P15 brain sections for NEUN (a pan-neuronal marker), CUX1 (an upper layer cortical neuron marker), and CTIP2 (enriched in lower layer cortical neurons and hippocampal granule cells) (Fig. 2c). Cortical thickness was reduced by 40% in Top1 cKO mice relative to WT mice (Fig. 2c, Supplementary Fig. 2a). While all cortical layers were affected by Top1 deletion, lower cortical layers showed the most prominent effect (~30% decrease in L2–4, ~70% decrease in L5, and ~40% decrease in L6) (Fig. 2c, Supplementary Fig. 2a). Hippocampal area was also drastically reduced (Supplementary Fig. 2b), with a stronger effect in CA1, CA2, and CA3 hippocampal regions (Fig. 2c). In contrast, the DG was not overtly affected, consistent with no loss of TOP1 in this region (Supplementary Fig. 1). Top1 cHET cortical thickness was comparable to WT (Supplementary Fig. 2a).

Given the profound reduction in cortical thickness, we next sought to understand the possible causes of this phenotype. To determine if the loss in cortical thickness was due to a deficit in cortical layering or to neurodegeneration, we compared Top1 cKO and cHET somatosensory cortex to that of WT during the first 2 weeks of postnatal development (Fig. 3a, b). Cortical neurogenesis and neuron migration begin at E11.5, when Neurod6Cre is first expressed28, and terminate prenatally around E17.5 (reviewed in ref. 29). At P0, the overall thickness and layer organization of Top1 cKO and cHET cortex were comparable to that of WT, indicating that neurogenesis and neuron migration were not affected. However, Top1 cKO cortical thickness was affected at later timepoints. In particular, L5 and L6 were more vulnerable to Top1 loss, showing a significant decrease in thickness compared to WT at P7, and a collapse in thickness by P15. L2–4 were only significantly reduced at the P15 timepoint. Top1 cHET cortical development was comparable to that of WT mice (Fig. 3a, b). These data suggest that homozygous loss of Top1 caused rapid, early-onset neurodegeneration that initially affected lower layer neurons and then extended to upper layers.

Fig. 3: Neurodegeneration of the cerebral cortex in Top1 cKO mice.
figure 3

a WT and Top1 cKO cerebral cortex immunostained for CUX1 and CTIP2 at P0, P2, P7, and P15. Images are representative of three independent experiments for a total of three mice per genotype per time point. Scale bar = 100 μm. b Cortical layer thicknesses, n = 3 per genotype per time point. n.s.p > 0.05, *p < 0.05, **p < 0.01, and ****p < 0.0001. Asterisks refer to WT vs. cKO comparisons. WT vs. cHET p values were >0.05 in all comparisons. WT vs. cKO p values in all layers: at P0 p = 0.43, at P2 p = 0.003, at P7 p = 0.029, at P15 p = 0.002. WT vs. cKO p values in L2–4: at P0 p = 0.38, at P2 p = 0.052, at P7 p = 0.57, at P15 p = 0.016. WT vs. cKO p values in L5: at P0 p = 0.28, at P2 p = 0.070, at P7 p = 0.010, at P15 p < 0.0001. WT vs. cKO p values in L6: at P0 p = 0.47, at P2 p = 0.011, at P7 p = 0.008, at P15 p = 0.012. One-way ANOVA. c Gradual loss of L5 CTIP2high neurons in Top1 cKO cortex. Scale bar = 20 μm. Images are representative of three independent experiments for a total of three mice per genotype for P0, P7, and P15 and four mice per genotype for P2. d Quantification of L5 CTIP2high density and e soma size at the indicated time points. P0, P7, and P15, n = 3 for each genotype; P2, n = 3 WT, n = 4 cKO. n.s.p > 0.05. WT vs. cHET p values were >0.05 in all comparisons. n/a = not applicable because no neurons were present. One-way ANOVA with Dunnett’s multiple comparison test. Values are mean and error bars are ±SEM. n.s. not significant.

CTIP2/Bcl11b is a transcription factor that marks projection neurons in L5 and L6 and is highly expressed in L5 corticospinal motor neurons30. To evaluate the extent to which the decrease in L5 thickness was due to neuronal loss over time, we quantified the density and cell size of spinal projection neurons (CTIP2high). We found that CTIP2high neuron density in Top1 cKO was reduced relative to WT mice by P7, and these neurons were no longer present by P15 (Fig. 3c, d). While CTIP2high neuron density did not decline until P7, we observed a decrease in CTIP2high soma size beginning at P2 (Fig. 3e). These data suggest that deletion of Top1 affected CTIP2high L5 neurons as early as P2 and contributed to the demise of these neurons by P15. Since HET loss of Top1 did not affect any of the neurons or markers evaluated above, we did not examine Top1 cHET mice in subsequent experiments.

Top1 cKO mice show neuronal apoptosis and neuroinflammation

We next performed immunostaining for cleaved-caspase 3 (cl-CASP3) and terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL), markers of intermediate and late phases of apoptosis, respectively. Both markers were increased in Top1 cKO cortex at P7, particularly in L5 and L6 where cell loss and layer thinning were most pronounced (Fig. 4a, b, Supplementary Fig. 3a, b). Another early sign of apoptosis is cell shrinkage, which was observed in L5 neurons starting at P2 (Fig. 3c, e). The cl-CASP3 signal was localized in the soma and apical dendrite of L5 neurons (Fig. 4b), suggesting that neurons in this region were undergoing apoptosis. Altogether, these data indicate that the cortex develops normally in Top1 cKO mice up to birth, but then shows signs of neurodegeneration by P2 that initiates in lower layer excitatory neurons.

Fig. 4: Cell death and neuroinflammation in lower cortical layers of Top1 cKO mice.
figure 4

a P7 somatosensory cortex immunostained for TUNEL, cl-CASP3, and b (inset) NEUN. Dashed lines delineate cortical layering identified by NEUN staining. Arrows, late apoptotic cl-CASP3+/TUNEL+ neurons show low levels of NEUN. cl-CASP3 staining localizes to the soma and apical dendrites of affected L5 neurons. Images are representative of three independent experiments for a total of three mice per genotype. c P7 somatosensory cortex immunostained for IBA1, GFAP, and d (inset) NEUN. a, c Scale bar = 300 μm, b, d scale bar = 100 μm. Images are representative of three independent experiments for a total of three mice per genotype.

Neuroinflammation is seen in a variety of neurodegenerative diseases (reviewed in ref. 31). To determine if neuron loss in Top1 cKO mice was associated with astrogliosis and/or microgliosis, we immunostained P7 cortex for glial fibrillary acidic protein (GFAP) and ionized calcium-binding adaptor molecule 1 (IBA1), respectively. In contrast to WT mice, intense GFAP and IBA1 immunostaining was detected in Top1 cKO cortex in L5 and L6 at P7 (Fig. 4c, d), suggesting extensive neuroinflammation in Top1 cKO mice.

To evaluate neuroinflammation non-invasively, we performed in vivo imaging of peripheral benzodiazepine receptor (PBR) expression by positron emission tomography (PET) (Supplementary Fig. 4a, b). PBR is a mitochondrial protein found in the brain (mainly glial cells) and peripheral tissues32. At baseline, the brain has lower levels of PBR compared to peripheral tissues33. PBR expression is increased in many neurodegenerative diseases characterized by microglia activation, including AD, PD, and multiple sclerosis34. PET imaging of WT and Top1 cKO P15 mice injected with the radioisotope-labeled PBR ligand 18F-PBR11135 indicated a significant increase in the uptake of the ligand in the frontal lobe, cerebral cortex, and hippocampus of Top1 cKO brains relative to WT brains (Supplementary Fig. 4a, b). Increased 18F-PBR111 binding was also detected in sections of the cerebral cortex from Top1 cKO mice using autoradiography (Supplementary Fig. 4a).

Downregulation of long genes in Top1 cKO lower layer neurons

To evaluate the extent to which Top1 deletion causes downregulation of long genes in vivo, we performed a small-scale single-cell RNA-seq experiment with cortical cells derived from two WT and two Top1 cKO P7 mice. We captured a total of 1,596 cells (683 WT, 913 cKO) and identified a median of ~2,300 transcripts per cell that corresponded to a median of ~1,750 genes per cell. Using unbiased clustering analyses, we detected three main cell clusters, which we annotated as excitatory neurons, inhibitory neurons, and glial cells based on the expression of marker genes (Fig. 5a, Supplementary Data 1). We then investigated transcriptional changes between WT and cKO excitatory neurons. As expected, Top1 expression levels were drastically decreased in excitatory neurons from cKO animals (−1.08 log2 fold change; adjusted [adj.] p value = 7.95 × 10−23), whereas levels in inhibitory neurons (−0.43 log2 fold change; adj. p value = 0.99) and glial cells were similar between genotypes (−0.33 log2 fold change; adj. p value = 0.37) (Fig. 5b). We identified 132 downregulated genes and only one upregulated gene in excitatory neurons (Supplementary Data 2). Consistent with our previous findings23,24, the average length of the downregulated genes in cKO excitatory neurons was 2.5-fold longer than the average gene length of all genes expressed in cortical neurons (151.4 kb vs. 59.3 kb) (Fig. 5c and Supplementary Data 2). No biased change in long gene expression was seen in the inhibitory neurons or glial cell clusters (Fig. 5c).

Fig. 5: Biased downregulation of long genes in lower layer excitatory neurons of Top1 cKO mice.
figure 5

a Expression levels of canonical marker genes, Neurod6, Gad1, and Aqp4, in the three main cell clusters identified by single-cell RNA-seq in P7 WT and cKO cortex (n = 2 mice/genotype). b Top1 expression levels in WT and cKO cells in each cell cluster. DESeq2 adj. c Mean expression change in bins of 200 genes by length in the different cell clusters. d In situ hybridization of Ptprd and Neurod6 transcripts in different cortical layers of P7 WT and cKO mice. Sections were also stained with DAPI. Scale bar = 10 μm. Images are representative of two mice per genotype and a total of 11 WT sections and 14 cKO sections. e CellProfiler output from analyses of the images shown in d. Neurod6+ neurons were colored based on the number of Ptprd transcripts identified. f Number of Ptprd transcripts/Neurod6+ neurons/section in cortical neuron layers of WT and cKO P7 cortex. Box is first to third quartile, line is median, error bars are minimum and maximum values, n.s.p > 0.05. Two-sided Student’s t test (n = 11 WT sections; n = 14 cKO sections; n = 2 mice per genotype). n.s. not significant.

In the excitatory neuron cluster, many of the downregulated genes were involved in axon extension and morphology (Celf2, Rtn4, Hspa5, Gpm6a, Zbtb18, Epha4, Gap43, Hspa5, Nefl, Ank2, Nefm, and Gpm6b) and in the induction of postsynaptic currents (Epha4, Snap25, Syt1, Nrxn1, Nrxn3, Cplx1, Snap91, and Snca) (Supplementary Data 2). These data were consistent with the loss of long projecting neurons and suggested that the function of excitatory circuits in Top1 cKO mice is affected. Genes involved in cholesterol biosynthesis and metabolic pathways (Scd2, Sqle, Hmgcs1, and Hmgcr) and genes relevant to AD (App, Ppp3cb, Atp2a2, Calm2, and Scna) were also downregulated (Supplementary Data 2). Top1 cKO mice present a similar, but more severe, phenotype relative to mice depleted of mitogen-activated protein kinase 1/2 (MAPK1/2) in excitatory postmitotic neurons36. Consistent with this observation, many of the downregulated genes were involved in the MAPK signaling pathway (Cdc42, Mef2c, Ppp3cb, Hspa5, and Akt3). We also found many downregulated genes involved in calcium regulation (Gnao1, Ywhaq, Camk4, Gnas, Atp2a2, Calm3, and Calr).

Given the increased vulnerability of lower layer Top1 cKO neurons to neurodegeneration, we asked whether long genes were more strongly affected in lower layer neurons compared to upper layer neurons. The small scale of our single-cell RNA-seq experiment precluded us from resolving upper and lower layer neuron clusters. Thus, we performed single-molecule in situ hybridization for Ptprd (Fig. 5d–f) (2 P7 mice per genotype, n = 11 WT sections; n = 14 cKO sections), the longest gene downregulated in cKO excitatory neurons (length 2.27 Mb; log2 fold change; −0.75; adj. p value <1.12 × 10−6) (Supplementary Data 2). To restrict our analysis to Neurod6+ excitatory neurons, we co-hybridized the sections with a probe to Neurod6 and used DAPI (4′,6-diamidino-2-phenylindole) to label all cells (Fig. 5d). We then used CellProfiler to quantify the number of Ptprd transcripts in Neurod6+ neurons (Fig. 5d–e; total number of Neurod6+ neurons identified: L2–4 WT 16,090, L2–4 cKO 18,401, L5 WT 13,929, L5 cKO 7,799, L6 WT 8,727, and L6 cKO 5,718). We observed a small decrease in Neurod6 transcripts in L5 cKO neurons compared to WT, consistent with Neurod6 being one of the downregulated genes in Top1 cKO mice, and no change in L2–4 and L6 neurons (Supplementary Fig. 5a). The percentage of Neurod6+ neurons in L2–4 was similar between WT and cKO cortical sections, while in L5 and L6 the percentage of Neurod6+ neurons was lower in cKO relative to WT (Supplementary Fig. 5b), consistent with loss of lower layer excitatory neurons at P7. While the number of Ptprd transcripts/Neurod6+ neuron was comparable in upper layers between WT and Top1 cKO mice, the number of Ptprd transcripts/Neurod6+ neuron was significantly reduced in L5 and L6 neurons of Top1 cKO mice (Fig. 5d–f), demonstrating reduced expression of this extremely long gene in lower, but not upper, layer neurons at P7.

Elevated mutation burden in Top1 cKO neurons

TOP1 inhibition or deletion in mitotic cells induces DNA damage and genomic instability37,38,39,40. To evaluate the extent to which Top1 deletion causes DNA damage in postmitotic neurons, we immunostained P0, P2, and P7 cortex for γH2AX, a marker of double-strand DNA (dsDNA) breaks. At P0 and P2 timepoints, levels of γH2AX were similar between WT and Top1 cKO mice (Supplementary Fig. 6a). At P7, roughly one-third of neurons presented γH2AX foci in Top1 cKO cortex. In contrast, only 3% of neurons showed γH2AX staining in P7 WT cortex (32.6 ± 5.42% neurons with γH2AX foci in Top1 cKO vs. 3.2 ± 2.6% neurons with γH2AX foci in WT; p value = 0.008, two-sided Student’s t test; data are the mean of percentages of neurons with γH2AX foci; n = 3 mice per genotype) (Fig. 6a). γH2AX accumulation in Top1 cKO mice extended to all cortical layers, although it was more pronounced in L6 (Fig. 6a–c, Supplementary Fig. 6b). Increased DNA damage in Top1 cKO cortex was further confirmed by immunostaining with phosphorylated p53-binding protein 1 (Supplementary Fig. 6c, d), another marker of dsDNA breaks41.

Fig. 6: Elevated DNA damage and more abundant CNVs in Top1 cKO mice.
figure 6

a P7 somatosensory cortex immunostained for γH2AX. Dashed lines delineate the cortical layering identified by NEUN (not shown). Scale bar = 300 μm, b insets of P7 Top1 cKO cortical layers immunostained with NEUN and γH2AX, showing γH2AX foci. Scale bar = 20 μm. Images are representative of three independent experiments for a total of three mice per genotype. c Percentages of neurons with γH2AX foci in different layers of WT and cKO P7 cortex. Values are expressed as mean and error bars are ±SEM. Two-sided Student’s t test. n = 3 mice per genotype. d Graph showing the overlap of all CNVs identified in WT and cKO neurons at the different genomic locations. Y-axis indicates the number of CNVs identified at the correspondent genomic location; above zero are duplications (dup), below zero are deletions (del). (Inset) CNV coverage, number of CNVs identified, and percentages of neurons with CNVs in WT and cKO mice.

Extensive DNA damage, if not properly repaired, can increase somatic mutation burden. To evaluate copy number variations (CNVs) at the single-cell level, we isolated a small number of neurons (n = 39 WT; n = 43 cKO) by fluorescence-activated cell sorting (FACS) from P7 cerebral cortex of one WT and one Top1 cKO mouse (Supplementary Fig. 10). We identified an increase in the number of cKO neurons with CNVs compared to WT neurons (4/39 in WT; 14/43 in cKO) (Supplementary Fig. 6e). We repeated the experiment using a droplet-based whole-genome amplification (WGA) approach on larger groups of neurons from a different pair of mice42. A two-fold increase in CNV prevalence was detected in cKO neurons (24/123 in WT; 60/169 in cKO) (Fig. 6d, Supplementary Data 3), further supporting the previous results. These data suggest that TOP1 plays a key role in maintaining genomic integrity in postmitotic neurons.

NAD+ supplementation reduces neuronal death in Top1 cKO mice

PARP1 catalyzes the addition of poly-ADP ribose (PAR) to multiple substrates and consumes NAD+ in the process18,19,20. In DNA damage-induced neurodegenerative diseases, PARP1 is hyperactive and leads to increased PAR levels, energetic breakdown, and cell death17,18,19,20. Given the extensive DNA damage observed in neurons from Top1 cKO mice, we next evaluated the extent to which PARP1 levels and activity were changed via western blot analysis for PARP1 and its post-translational modification PAR, in WT and Top1 cKO P7 cortical lysates. We found an increase in both PARP1 and PAR levels in Top1 cKO cortical lysates relative to WT lysates (Fig. 7a, b, Supplementary Fig. 11), suggesting that deletion of Top1 causes an increase in PARP1 activity.

Fig. 7: Increased PARP1 and PAR levels in Top1 cKO cortex.
figure 7

a Western blot analysis and b quantification of PARP1 and PAR levels in P7 cortical lysates from three mice per genotype. GAPDH was used as a loading control. Protein levels are normalized to GAPDH and expressed as mean fold change relative to WT. Error bars are ±SEM. Two-sided Student’s t test. n = 3 mice per genotype, three technical replicates.

NAD+ supplementation was found to increase neuronal survival in models of neurodegeneration and to restore NAD+ levels in response to PARP1 hyperactivation18,43. Therefore, we hypothesized that increasing NAD+ levels may limit neurodegeneration in Top1 cKO mice. We first evaluated the extent to which two precursors of NAD+ synthesis, nicotinamide mononucleotide (NMN) and nicotinamide riboside (NR), elevated NAD+ in the neonatal mouse brain. We found that only NR elevated NAD+ levels in the brain of P3 mice when injected intraperitoneally (i.p.) (Supplementary Fig. 7). To measure the amounts of NAD+ in WT and Top1 cKO mice and test whether daily injections of NR could maintain high levels of NAD+ over time, we injected i.p. WT and Top1 cKO mice with saline (control) or NR (200 mg/kg per day) beginning on P1 and quantified NAD+ levels in cortical extracts at P7 and P15 (Table 1). At both time points, NR-treated WT and Top1 cKO mice showed an increase in NAD+ levels compared to saline-treated mice (Table 1), confirming that NR was efficiently delivered to the postnatal brain with chronic treatment.

Table 1 Quantification of NAD+ cortical levels in WT and cKO mice treated with saline or NR.

NAD+ cortical levels in Top1 cKO mice were comparable to WT controls at P7 (94.8 ± 2.4 in P7 WT saline vs. 94.7 ± 6.2 in P7 Top1 cKO saline) (Table 1), consistent with the fact that only a small number of cortical neurons were undergoing energetic breakdown and apoptosis at this age (Fig. 4a, b, Supplementary Fig. 3a, b). Untreated WT mice showed an ~44% increase in NAD+ levels in the cortex from P7 to P15 (94.8 ± 2.4 in P7 WT saline vs. 136.7 ± 10.9 in P15 WT saline). In contrast, NAD+ levels did not increase from P7 to P15 in Top1 cKO cortical samples (94.7 ± 6.2 in P7 Top1 cKO saline vs. 92.8 ± 6.6 in P15 Top1 cKO saline) and showed an ~32% decrease relative to WT controls at P15 (136.7 ± 10.9 in P15 WT saline vs. 92.8 ± 6.6 in P15 Top1 cKO saline). Treatment with NR for 15 days restored NAD+ levels (136.7 ± 10.9 in P15 WT saline vs. 155.5 ± 22.9 in P15 Top1 cKO NR) (Table 1). These data indicated that Top1 cKO mice developed a deficit in cortical levels of NAD+ by P15 and suggested that cortical NAD+ levels could be restored by supplementation with NR.

We next evaluated the extent to which long-term NAD+ supplementation rescued motor defects and delayed premature death of Top1 cKO mice. NR treatment did not rescue the motor deficits of Top1 cKO mice (Fig. 8a), but NR treatment did increase the median survival of Top1 cKO mice by 5 days (18 days in saline injected vs. 23 days in NR treated), which corresponds to a 30% increase in lifespan (Fig. 8b).

Fig. 8: NAD+ supplementation with nicotinamide riboside partially blocks neurodegeneration and increases lifespan of Top1 cKO mice.
figure 8

a P7 righting assay (left) and P12 geotaxis (right) performed on WT and Top1 cKO mice treated with saline or NR 200 mg/kg per day from P1 onward. For P7: n = 12 WT;saline mice, n = 12 WT;NR mice, n = 8 cKO;saline mice, n = 12 cKO;NR mice. For P12: n = 14 WT;saline mice, n = 14 WT;NR mice, n = 5 cKO;saline mice, n = 14 cKO;NR mice. Dashed lines represent cutoff time. n.s.p > 0.05. One-way ANOVA with Dunnett’s multiple comparison test. b Kaplan–Meier survival curve of Top1 cKO mice treated with saline or 200 mg/kg per day NR from P1 onwards. Mantel–Cox test. WT = 11, cKO = 10 mice. c Top1 cKO mice were treated with saline or 200 mg/kg per day NR for 6 days starting from P1 and then brains were collected. Sections containing cortex (Ctx) and hippocampus (Hip) were immunostained and for cl-CASP3, TUNEL, GFAP, and IBA1 (left panel), scale bar = 500 μm. The number of cells positive for each marker was quantified (right panel). n.s.p > 0.05. Two-sided Student’s t test. For cl-CASP3 quantification n = 4 mice per condition, for TUNEL, GFAP, and IBA1 quantifications n = 4 cKO;saline mice, n = 3 cKO;NR mice. d CTIP2 staining of cerebral cortex and hippocampus of P15 Top1 cKO mice treated with saline or 200 mg/kg per day NR for 14 days. Scale bar = 300 μm. Dashed lines delineate cortical layering and hippocampus based on NEUN, CUX1, and CTIP2 staining. The solid line indicates the area used to quantify cortical thickness. Images are representative of at least three independent experiments for a total of three mice per genotype. e Hippocampal area and number of CTIP2+ cells per section of cortex and hippocampus. n.s.p > 0.05. Two-sided Student’s t test. For thickness and area quantifications: n = 3 WT mice, n = 6 cKO;saline mice, n = 5 cKO;NR mice. For L5-6 CTIP2+ neurons quantification: n = 3 WT mice, n = 6 cKO;saline mice, n = 4 cKO;NR mice. For CA1 CTIP2+ neurons quantification: n = 3 WT mice, n = 3 cKO;saline mice, n = 4 cKO;NR mice. Two sections per mouse were used for all quantifications. Values are mean and error bars are ±SEM. n.s. not significant.

To determine if NR treatment also reduced neuroinflammation and cell death in Top1 cKO mice, we immunostained NR-treated Top1 cKO P7 brain sections for cl-CASP3, TUNEL, GFAP, and IBA1. We found that cl-CASP3 activation and TUNEL staining were greatly reduced throughout the somatosensory cortex and hippocampus in NR-treated mice (Fig. 8c). Neuroinflammation was also strongly reduced, as evidenced by reduced IBA1 and GFAP staining (Fig. 8c). NR treatment also modestly increased hippocampal area, increased overall cortical thickness, and increased lower layer thickness in cKO mice at P15 (Fig. 8d, e). Moreover, we observed a 2- to 3-fold increase in the number of CTIP2+ neurons in lower cortical layers and in the hippocampus of Top1 cKO mice treated with NR (Fig. 8d, e). These data suggest that neuron loss is only partially dependent on NAD+ depletion.

p53 loss partially rescues neurodegeneration in Top1 cKO mice

We asked whether partial or complete deletion of p53 could rescue neuron death in Top1 cKO mice. To answer this question, we crossed Neurod6Cre/+::Top1fl/fl mice with p53 KO mice44 to generate WT and Top1 cKO mice with p53 WT, HET, or KO alleles. Mice were assayed for motor tests at P7 and P12, brains were collected at P15 and cortical thickness was quantified by staining with CUX1 and CTIP2. p53 deletion failed to rescue motor deficits (Fig. 9a) and did not extend lifespan in a small cohort (n = 2) of Top1 cKO::p53 KO animals, which died in the third postnatal week. However, both homozygous and HET loss of p53 led to an ~1.5-fold increase in cortical thickness and an ~2.5-fold increase in hippocampal area in Top1 cKO mice (Fig. 9b, c), bringing these areas to ~60% of Top1 WT size. The rescue observed in Top1 cKO::p53 KO and Top1 cKO::p53 HET cortex was caused by an ~3-fold increase in L5 thickness and an ~2-fold increase in L6 thickness, bringing L5 from ~18% to ~52% of Top1 WT L5 size and L6 from ~28% to 55% of Top1 WT L6 size (Fig. 9b, c). Both homozygous and HET loss of p53 in Top1 cKO mice led to an increase in the number of CTIP2+ neurons in lower cortical layers and the CA1 hippocampal region. We observed a complete rescue in the number of CTIP2+ neurons of the CA1 hippocampal region in Top1 cKO::p53 KO mice (Fig. 9b, c). To test whether the increase in cortical and hippocampal size in Top1 cKO::p53 KO mice was due to an increase in the number of TOP1 neurons, we performed TOP1 and NEUN immunostaining of the cortex and hippocampus. While very few TOP1/NEUN+ neurons were observed in the lower cortical layers and CA1 hippocampal region of Top1 cKO::p53 WT mice, these areas were almost completely composed of TOP1/NEUN+ neurons in Top1 cKO::p53 KO (Supplementary Fig. 8). These data strongly suggest that neurodegeneration caused by Top1 loss is partially p53 dependent.

Fig. 9: Deletion of p53 partially blocks neurodegeneration but does not rescue behavioral deficits in Top1 cKO mice.
figure 9

a Righting assay performed at P7 and geotaxis assay performed at P12 with the indicated genotypes. n.s.p > 0.05. One-way ANOVA with Dunnett’s multiple comparison test. For P7 n = 5 p53 WT::Top1 cKO mice, n = 16 p53 HET::Top1 cKO mice, n = 6 p53 KO::Top1 cKO mice, n = 10 p53 WT;HET;KO::Top1 WT mice. For P12 n = 4 p53 WT::Top1 cKO mice, n = 13 p53 HET::Top1 cKO mice, n = 5 p53 KO::Top1 cKO mice, n = 10 p53 WT;HET;KO::Top1 WT mice. b Cerebral cortex and hippocampus from P15 mice. Genotypes of the Top1 and p53 alleles are indicated. Sections were immunostained for CUX1, CTIP2, and NEUN. Dashed lines are based on NEUN, CUX1, and CTIP2 staining and delineate cortical layering and hippocampus. Only CTIP2 staining is shown. Scale bar = 300 μm. Images are representative of at least three independent experiments for a total of at least three mice per genotype. c Quantifications of cortical thickness, hippocampal area, and number of CTIP2+ neurons per section in cortical layers and the CA1 region of the hippocampus. n.s.p > 0.05. One-way ANOVA with Dunnett’s multiple comparison test for each cortical layer of hippocampal area. For cortical thickness quantifications: n = 6 p53 WT::Top1 cKO mice, n = 3 p53 HET::Top1 cKO mice, n = 3 p53 KO::Top1 cKO mice. Two sections per mouse. For hippocampal area quantifications: n = 3 p53 WT::Top1 cKO mice, n = 3 p53 HET::Top1 cKO mice, n = 3 p53 KO::Top1 cKO mice. Two sections per mouse. For L5 CTIP2 quantifications: n = 6 p53 WT::Top1 cKO mice, n = 3 p53 HET::Top1 cKO mice, n = 3 p53 KO::Top1 cKO mice. Two sections per mouse. For L6 CTIP2 quantifications: n = 6 p53 WT::Top1 cKO mice, n = 3 p53 HET::Top1 cKO mice, n = 2 p53 KO::Top1 cKO mice. Two sections per mouse. For CA1 CTIP2 quantifications: n = 3 p53 WT::Top1 cKO mice, n = 3 p53 HET::Top1 cKO mice, n = 2 p53 KO::Top1 cKO mice. Two sections per mouse. Values are mean and error bars are ±SEM. n.s. not significant.


Our data support a model whereby loss of TOP1 causes transcriptional stress in postmitotic neurons that leads to high levels of DNA damage, subsequent activation of DNA damage-induced cell death pathways and neurodegeneration (Supplementary Fig. 9). Interestingly, aberrant TOP1 activity has been shown to cause a similar phenotype in neurodegenerative genome instability syndromes45,46. In these pathologies, the formation of stable TOP1cc’s at active transcription sites induces transcriptional arrest, accumulation of RNA:DNA hybrids (R-loops), and the formation of dsDNA breaks in postmitotic cells46,47. TOP1 deficiency has also been linked to transcriptional stress, accumulation of R-loops, and genomic instability in mitotic cells38,40,48,49. DNA damage caused by TOP1 depletion was attributed to the collision between transcriptional machinery and the DNA replication fork40. Our data suggest that TOP1 loss induces DNA damage accumulation independent of DNA replication in postmitotic neurons, possibly because of increased DNA torsional stress and R-loop formation during transcription. Further investigation will be required to understand the extent to which R-loops accumulate in Top1 cKO neurons. Altogether, these data indicate that TOP1 maintains genomic integrity in the central nervous system.

Another interesting relationship between Top1 deletion and TOP1cc formation is the downstream activation of multiple DNA damage-induced pathways, including p53 activation45 and increased PARP1 activity17. Consistent with other forms of neurodegeneration that feature DNA damage, Top1 cKO mice show increased PARP1 activity, reduced NAD+ levels, neuroinflammation, and neuronal death18,19,20. Our study suggests that Top1 cKO mice could be used to further understand the pathways involved in DNA damage-induced neurodegeneration in vivo, but on a greatly accelerated time scale.

We also found that treatment with NR restored NAD+ levels in the brain of Top1 cKO mice. This treatment increased lifespan by 30%, significantly reduced neuroinflammation, and reduced neuron death, including CTIP2+ neurons in the lower cortical layers and hippocampus. These results corroborate other studies indicating that NAD+ supplementation can extend lifespan, decrease neuroinflammation, and delay neuron death in neurodegeneration models, including in AD and DNA-repair-deficient mouse models18,50,51,52. However, given that the cortical and hippocampal reduction were only modestly rescued by NR treatment, NAD+-independent pathways must also contribute to neurodegeneration in Top1 cKO mice.

In support of this possibility, genetic ablation of p53 led to a greater rescue in cortical thickness and hippocampal area compared to NR treatment and led to a near complete rescue in the number of CTIP2+ projecting neurons. The tumor suppressor p53 is the main driver of DNA damage-induced death in neurons and is a common downstream effector of multiple cellular stress sensors, including PARP120,53,54,55. However, neither p53 depletion nor NAD+ supplementation rescued the motor phenotypes and premature death observed in Top1 cKO mice. These data suggest that loss of TOP1 could have additional effects that compromise neuron function, such as elevating somatic mutation burden (Fig. 6d), transcriptional downregulation of long synaptic genes23,24,26 (Fig. 5c–f), which attenuates synaptic activity24, impaired RNA splicing56, and/or impaired ribosomal RNA biosynthesis49,57. Thus, transcriptional decline and somatic mutations could incapacitate neurons well before cell loss is apparent.

Selective vulnerability of different neuronal populations to cell death has been described in many neurodegenerative diseases and it has often been attributed to intrinsic properties of the affected neurons58. Our data indicate that among cortical neurons, lower layer cortical neurons are particularly sensitive to Top1 loss. Using single-cell RNA-seq and single-molecule in situ hybridization, we found that Top1 loss strongly impaired expression of long genes, with a bias for lower layer neurons. Many long genes encode proteins that play key roles in synapse formation and function. Downregulation of these genes is likely to compromise neuron physiology, as we previously found26, and health independent of DNA damage.

Alternatively, lower layer neurons could be more vulnerable because of their earlier birthdate and presumably earlier expression of Neurod6Cre. Cortical layers are produced in an inside-out order, where lower layers are produced earlier than upper layers29. Therefore, lower layer neurons have more time to accumulate transcriptional stress, DNA damage, and somatic mutations that affect neuronal functions and ultimately cause neurodegeneration. In support of this hypothesis, we observed that lower layer cortical neurons present higher levels of DNA damage and downregulation of long genes in Top1 cKO mice. However, countering this possibility, we found that L5 neurons are more vulnerable to Top1 deletion than L6 neurons, yet L5 neurons are born after L6 neurons.

The unique properties of L5 motor neurons, such as large soma size and the ability to establish extremely long distance axonal projections (requiring adhesion molecules that are encoded by long genes), are known to be more vulnerable to cell death36,59. Projection neurons that maintain a large soma, lengthy projections, and higher transcriptional output of long genes, likely consume more energy than local projection neurons. L5 upper motor neurons are thus likely to be more sensitive to NAD+ depletion and energetic breakdown than other neuronal populations. Interestingly, ALS and other motor neuron neurodegenerative diseases have been associated to defects in R-loop resolution60, providing another possible explanation for why this neuronal population is more sensitive to Top1 loss. Ultimately, future studies will be needed to characterize the effect of Top1 deletion in other neuronal subtypes, including inhibitory neurons and neurons from other brain regions.



All animal procedures were approved by the University of North Carolina at Chapel Hill Animal Care and Use Committee. Mice were housed at temperatures of 18–23 °C with 40–60% humidity with food and water provided ad libitum and maintained on a 12-h dark/light cycle. Top1fl/fl conditional mice were previously described24. Neurod6Cre mice28 and p53/− mice44 were obtained from Jackson Laboratory. Genomic DNA extracted from tail or ear samples was utilized for mouse genotyping by PCR using standard techniques. Primers for gene amplification are as follows (listed 5′–3′): Top1 geno2 GAGTTTCAGGACAGCCAGGA and Top1 geno3 GGACCGGGAAAAGTCTAAGC amplifying Top1 WT and KO and floxed alleles, CreF GATGGACATGTTCAGGGATCGCC and CreR CTCCCATCAGTACGTGAGAT amplifying the Cre allele; p53 WT-F CCCGAGTATCTGGAAGACAG and p53 WT-R ATAGGTCGGCGGTTCAT amplifying p53 WT allele; p53 ex7 TATACTCAGAGCCGGCCT and p53 Neo TCCTCGTCGTTTACGGTATC amplifying p53 KO allele.

Motor assays

For the righting assay, P7 pups were placed on their backs on a sheet of paper and held in position for 3 s. Pups were then released and the total time needed to flip on their feet was recorded. For the negative geotaxis assay, P12 pups were held for 5 s on a 45° incline with the head pointing downward. Pups were then released and the total amount of time needed to face upward was recorded. For both assays, a cutoff maximum of 60 s was given for every trial. Pups were tested three times with a break of 30 s between each trial. The times recorded for the three trials were then averaged. Top1 cKO and cHET mice were compared with WT littermates or age-matched mice. Males and females mice were used for motor assessments. GraphPad Prism (version 7.00) was used for statistical analysis.

Tissue collection and immunostaining

At the indicated time points, mice were anesthetized and perfused first with phosphate-buffered saline (PBS) and then with 4% paraformaldehyde (PFA). Brains were dissected, post fixed in 4% PFA overnight at 4 °C, incubated in 30% sucrose at 4 °C, and embedded in M-1 embedding matrix (Thermo Scientific, 1310). Brains were cut on a cryostat and free-floating sections were collected and stored in a freezing solution consisting of PBS, ethylene glycol, and glycerol. Sections were rinsed in PBS, treated with citrate buffer for 30 min at 95 °C, rinsed again in PBS followed by rinses with Tris-buffered saline containing Triton-X-100 (TBS/TX, 0.05 M Tris, 2.7% sodium chloride, 0.3% Triton-X-100, pH 7.6). Sections were blocked in 10% normal donkey serum in TBS/TX (NDS/TBS/TX) for 1 h and then incubated overnight at room temperature in primary antibody cocktails diluted in NDS/TBS/TX. Primary antibodies used were rabbit anti-TOP1 (1:300; GeneTex, GTX63013, EPR5375), guinea-pig anti-NEUN (1:400; EMD-Millipore, ABN90P), rabbit anti-CUX1 (1:200; Santa Cruz Biotechnology, sc-13024), rat anti-CTIP2 (1:200; Abcam, ab18465), rabbit anti-cleaved-CASP3 (1:100; Cell Signaling Technology, 9664), rabbit anti-IBA1 (1:400; Wako, 019-19741), goat anti-GFAP (1:750; Abcam, ab53554), rabbit anti-phospho-Histone H2A.X (1:50; Cell Signaling Technology, 2577), and phospho-53BP1 (Ser1778) (1:50, Cell Signaling Technology, 2675).

After incubation in primary antibodies, sections were rinsed in TBS/TX and blocked with NDS/TBS/TX for 30 min. All secondary antibodies were diluted at 1:200 in NDS/TBS/TX and applied for 6 h. These included donkey anti-rabbit IgG Alexa 488 or Alexa 568 (Thermo Fisher Scientific, A21206 and A10042, respectively), donkey anti-goat IgG-Cy3 (Jackson ImmunoResearch Laboratories, 705-165-003), donkey anti-rat IgG-Cy3 (Jackson ImmunoResearch Laboratories, 712-165-153), and donkey anti-guinea-pig IgG Alexa 647 (Jackson ImmunoResearch Laboratories, 706-605-148). DAPI (1:4000; Fisher Scientific, EN62248) was added to secondary antibody cocktails. Sections were then rinsed in TBS/TX and PBS. Detection of apoptotic cells by TUNEL assay was performed on previously immunostained tissue sections using the DeadEnd™ Fluorometric TUNEL System (Promega, G3250) following the manufacturer’s instructions. All stained sections were mounted onto SuperFrost Plus slides (Fisher Scientific, 12-550-15) and coverslipped with FluoroGel mounting medium (Electron Microscopy Sciences, 17985-10). Imaging was performed on a Zeiss LSM 710 confocal laser scanning microscope.

Image analysis and quantitation

Confocal images of somatosensory cortex were collected from individual brain sections for each animal. At least two animals per condition and two sections per animal were used for every quantification. For neocortical layer-thickness analysis, images were transferred to ImageJ and individual layer boundaries were determined by the changes in density and appearance of NEUN, CUX1, and CTIP2 labeling. Layer thickness was measured using the “straight line” tool present in ImageJ. Measurements were expressed as absolute numbers or normalized to control samples and expressed as fold changes. For cell density and cell area quantification of CTIP2+, cl-CASP3+, TUNEL+, IBA1+, and GFAP+ cells a general pipeline was written on ImageJ and parameters were adapted based on the intensity and distribution of the specific cell-type markers. Briefly, brain sections where co-stained with the cell marker of interest and NEUN. Images of the cortex were manually cut into the different layers based on NEUN labeling. CUX1 and CTIP2 were also used to distinguish different layers. The channel of the cell marker of interest was then selected and a pixel-intensity threshold was set manually by an observer blind to the genotype. The same pixel-intensity threshold for every marker was applied to all layers and all genotypes. For CTIP2high cell density analysis, a threshold that allows the visualization of only highly expressing CTIP2 cells of L5 was chosen. After watershed segmentation, the binary image mask was analyzed using the particle analysis tool to count the number of events. The total number of particles and particle area were then measured using the ROI Manager tool in ImageJ. The total number of cells identified within a cortical layer was divided by the area of that layer.

To measure the percentage of neurons with γH2AX foci, we immunostained brain sections for NEUN and γH2AX. Images were processed in ImageJ and a layer-specific mask on NEUN+ cells was created as described above. Then, the γH2AX signal was selected and the number of γH2AX foci was determined using the “find maxima” function in ImageJ. Briefly, a noise-tolerance threshold that allows the detection γH2AX foci was selected by an observer blind to the genotype and applied to all samples. A binary image of γH2AX foci was created through the single points option. The NEUN+ cell mask was then overlapped to the γH2AX foci binary image using the ROI Manager tool and the RawIntDen within each neuron was calculated. The RawIntDen was then divided to the value of a single pixel (255) in order to calculate the number of γH2AX foci per neuron. Representative images have been cropped and equally adjusted for brightness and contrast in ImageJ for presentation. GraphPad Prism (version 7.00) was used for statistical analysis.

PET imaging with 18F-PBR111

PET imaging probe of PBR ligand, 18F-PBR111, was produced at the UNC BRIC Cyclotron and Radiochemistry Core facility according to a well-established radiosynthesis method61. Radiochemical purity was >95% confirmed from the HPLC assay. Animal PET/CT imaging was conducted in the UNC Small Animal Imaging facility using a small animal PET/CT scanner (Argus, SEDECAL Inc., Spain) with a spatial resolution of 1.2 mm in the center field of view. Animals were anesthetized with isoflurane inhalation (1.5–2.5% isoflurane mixed with oxygen). A catheter was placed in the abdominal region for i.p. injection of radiotracer. WT and Top1 cKO P15 mice were placed on the imaging bed. 18F-PBR111 (~5 MBq in 50 µl) was administered to each animal through an i.p. catheter, followed by a 60-min dynamic scan. The computed tomography (CT) scan was conducted before the PET scan for attenuation correction and structure reference. Dynamic data were binned into six frames with 10 min/frame. Images were reconstructed using the 2D-OSEM (two-dimensional-ordered subset expectation maximization) algorithms with scatter, attenuation, and decay correction. Standardized uptake value was calculated by normalizing the signal to the injection dose and animal body weight. After PET/CT images, brains were collected and autoradiography was conducted using a digital phosphor imaging system (Cyclone Plus storage phosphor system, PerkinElmer Inc.). GraphPad Prism (version 7.00) was used for statistical analysis.

Drop-seq procedure

P7 mice were decapitated and cortices were isolated, cut into pieces with a sterile razor blade, and incubated in papain diluted in standard artificial cerebrospinal fluid (aCSF) media (NaCl 124 mM, KCl 2.5 mM, NaH2PO4 1.2 mM, NaHCO3 24 mM, HEPES 5 mM, glucose 13 mM, MgSO4-7H2O, 2 mM, CaCl2-2H2O 2 mM, pH 7.3) supplemented with (2R)-amino-5-phosphonovaleric acid (APV) and tetrodotoxin (TTX) at 37 °C for 30 min. Cortical pieces were then washed and gently dissociated in aCSF media with APV and TTX. Cortical cells were then filtered, captured, and processed into single-cell transcriptomes using Drop-seq62. Complementary DNA libraries were sequenced on two lanes of a HiSeq2500 on Rapid Run mode. FASTQ files were processed using the Drop-seq Toolkit 1.2 where possible and aligned to the mouse genome (mm10) using STAR63. Barcoded bead synthesis errors were corrected using a publicly available command line script64.

Single-cell RNA-seq bioinformatics

Cells expressing fewer than 300 different genes or whose mitochondrial transcripts exceeded 10% were excluded. Genes expressed in fewer than three cells were removed. The resulting cell × gene matrix was median centered and log normalized to generate the final gene expression matrix (1596 cells × 11,112 genes). Louvain clustering was performed on the top 48 principal components (based on eigenvalues greater than randomly permutated data [n = 1000]) using a silhouette score-optimized nearest-neighbor parameter of (67 nearest neighbors27). Cluster-specific marker genes were detected using a presence–absence binomial test (mean log2 fold change >1.0, p value < 0.05). Differentially expressed genes were identified using DESeq2 (adj. p value < 0.0565). To generate plots showing change in expression by gene length, genes were ordered by gene length and binned into groups of 200. The average fold change (calculated by DESeq2) was plotted against the average gene length for each bin in each cluster.

Single-molecule in situ hybridization and image analysis

RNAscope fluorescent multiplex assay was performed following the manufacturer’s instructions with the following changes. To avoid tissue deterioration, unfixed frozen sections of P7 cortex were fixed in fresh 4% PFA for 20 min and protease treatment was reduced to 10 min. The following probes were obtained from ACDbio: Mm-Neurod6-C3 (cat. no. 444851-C3), Mm-Ptprd (cat. no. 474651). Images from two mice per genotypes (n = 11 WT sections, n = 14 cKO sections) were acquired on a Zeiss LSM 710 confocal laser scanning microscope at ×40. Multichannel images were opened in ImageJ and manually separated into different layers based on DAPI labeling and separated in the different channels. Ptprd and Neurod6 channels were then selected and a pixel-intensity threshold was set manually to normalize the background among images of the different genotypes. A pixel-intensity threshold was also applied to DAPI images and followed by watershed segmentation. The observer was blind to the genotype. Binary images were then processed on CellProfiler ( using a custom-designed pipeline. Briefly, single cells and Neurod6 transcripts were identified as objects using the corresponding channels. Then, Neurod6 transcripts were assigned to each cell as children objects and quantified. Neurod6+ cells were selected by applying a threshold of 5 Neurod6 transcripts per cell. Single Ptprd transcripts or clusters were distinguished using a size threshold and were each assigned to Neurod6+ cells. Images showing the number of Ptprd transcripts/Neurod6+ cells was then generated by the DisplayDataOnImage function. The average number of single Ptprd transcripts or Ptprd clusters/Neurod6+ cell/section was the calculated. The final number of Ptprd transcripts/Neurod6+ cell/section was calculated with the following formula: # Ptprd transcripts/Neurod6+ cell/section = number of single Ptprd transcripts/Neurod6+ cell + (#Ptprd clusters/Neurod6+/section divided by the average area of single Ptprd transcripts/section). GraphPad Prism (version 7.00) was used for statistical analysis.

CNV analyses of FACS sorted cortical neurons

P7 cortices were dissected with the hippocampus removed and frozen at −80 °C. Frozen cortices were dissociated mechanically. Nuclei were purified using an iodixanol cushion66 and stained for NEUN (anti-human NeuN Alexa Fluor 555 conjugate (Millipore, MAB377)) and SYTO 13 green fluorescent nucleic acid stain (Thermo Fisher, S7575). NEUN+/SYTO 13+ neuronal nuclei were isolated by flow sorting into 8-well thin-wall PCR tube strips42. For the initial low cell number experiment, WGA was performed using a modified multiple annealing and loop-based (MALBAC) approach67. Single-cell libraries of 39 WT neurons and 43 cKO neurons extracted from one mouse per genotype were individually barcoded and prepared for Illumina sequencing using NextFLEX (BIOO Scientific, Austin, TX) following the manufacturer’s instructions. Sequencing was performed on an Illumina HiSeq RAPID platform. CNVs were detected using an unbiased CNV detection approach42. WGA quality control using Bayesian information criteria (>−1.5) removed 13 cells from subsequent analysis, and copy number states <1.22 and >2.82 were determined to define CNVs in DNAcopy (α = 0.001, undo.SD = 0, min.width = 5) segmentation. BWA (version 0.7.12) was used to align Illumina single-end reads to the genome. Samtools (v1.1) was used to generate BAM files. Picard Tools (v1.105) was used to remove duplicate reads. Bedtools (v2.17.0) was used to count aligned reads in genomic bins. R (v3.4.1) was used to normalize binned read counts to copy number estimates, segment bin values (DNAcopy, v1.50.1), and plot CNV profiles (ggplot2, v2.2.1). R was also used to fit Gaussian distributions to dataset-wide segment data to determine CNV thresholds (mixtools, v1.1.0).

For the follow-up experiment, 10× sequencing data from 123 WT and 169 cKO NEUN+/SYTO 13+ sorted cortical neurons derived from one mouse per genotype were aligned to the mouse genome (mm10) using CellRanger-dna cnv (version 1.1.0). Single-cell BED files were extracted from CellRanger output using SAMtools (version 1.9), BAMtools (version 2.5.1), and BEDtools (version 2.15.0), and then were uploaded to Ginkgo68 for CNV analysis using default parameters. Following Ginkgo CNV analysis, segmentation results were downloaded and filtered to remove likely false-positive CNVs. Regions containing six or more CNVs were considered to be “hotspots” for false-positive CNVs, and any CNVs located entirely within the boundaries of a hotspot were excluded. To further safeguard against false positives, CNVs under 5 Mb in length were also excluded. Bin level copy number estimates for all single cells were downloaded from Ginkgo and plotted with filtered CNV results in R (version 3.4.1) using ggplot2 (version 2.2.1) to generate CNV profiles.

Western blotting

P7 cortices were dissected from both Top1 cKO and WT control mice and lysed in RIPA buffer (0.05 M Tris-HCl, pH 8, 0.15 M NaCl, 0.5% deoxycholic acid, 1% NP-40, and 0.1% sodium dodecyl sulfate (SDS)), Halt Protease Inhibitor Cocktail (Thermo Fisher, 87785), and Halt Phosphatase Inhibitor Cocktail (Thermo Fisher, 78420). Lysates were sonicated and cleared by centrifugation. Protein concentration was determined using the Pierce BCA Protein Assay Kit (Fisher, 23227). Equal amounts of protein were denatured in reducing sample buffer, separated by SDS-PAGE (polyacrylamide gel electrophoresis) gels, and blotted to nitrocellulose membranes (Bio-Rad). Blots were blocked with Odyssey Blocking Buffer (Fisher, 927-40000) for 1 h at room temperature, and then incubated overnight at 4 °C with primary antibodies. The primary antibodies used were rabbit anti-PARP (1:1000, Cell Signaling, 9532) rabbit anti-PAR/pADPr (1:1000, R&D Systems, 4336-APC-050), and mouse anti-GAPDH (1:1000, Thermo Fisher, MA5-15738). After washing with TBS containing 0.5% Tween 20 (TBS-T), membranes were incubated with goat anti-mouse IRdye 680 (1:10,000 Licor Odyssey, 925-68070) and IRDye 800CW donkey anti-rabbit (1:10,000 Licor Odyssey, 926-32213) diluted in Odyssey Blocking Buffer 1 h at room temperature. Blots were washed with TBS-T and detection was performed with the Odyssey CLx Imaging System (Li-COR) using the Image Studio Software (Odyssey). GraphPad Prism (version 7.00) was used for statistical analysis.

NR treatment

Nicotinamide riboside chloride powder (Medkoo, 329479) was diluted to 10 mg/ml stock solution in saline, aliquoted, and stored at −80 °C. Neurod6Cre/+::Top1fl/+ males were bred with three Top1fl/fl females for 48 h. After 14 days, pregnant females were moved in a separate cage and checked for P0 pups twice a day. Twenty-four hours after birth, P1 pups were injected intraperitoneally with 20 µl/g of saline or NR once a day (final 200 mg/kg per day of NR). Entire litters were injected with saline or NR in a blinded manner. At P7 and P12, pups were assayed for righting and geotaxis assays, respectively, and genotyped. Mice were monitored every day. An independent set of litters treated as described was sacrificed at P7 or P15 for immunofluorescence analysis and NAD+ quantification. Brains were collected at the indicated time points of treatment, and after 1 h from the last injection, half of the brain was drop-fixed in 4% PFA for immunostaining and half was divided into pieces and flash-frozen for NAD+ quantification. GraphPad Prism (version 7.00) was used for statistical analysis.

NAD+ quantifications

Cortices were dissected from WT and Top1 cKO mice and flash-frozen in pieces ranging from 15 to 30 mg in weight. Cortical samples were collected 1 h after the last i.p. injection with saline, NR, or NMN. All cortical samples were thawed and processes for NAD+ quantification at the same time using EnzyChrom NAD+/NADH Assay Kit (BioAssay Systems, E2ND-100) following the manufacturer’s instructions. NAD+ quantification were collected using Synergy 2 microplate reader (Biotek) and using the Gen5 (version 2.0) software. The resulting NAD+ concentration was multiplied to the final volume of reagents for each sample and divided by the total amount of starting tissue to calculate NAD+ pmol/mg of tissue. GraphPad Prism (version 7.00) was used for statistical analysis.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.