The initial rostrocaudal patterning of the neural tube leads to differential expression of Hox genes that contribute to the specification of motor neuron (MN) subtype identity. Although several 3′ Hox mRNAs are expressed in progenitors in a noisy manner, these Hox proteins are not expressed in the progenitors and only become detectable in postmitotic MNs. MicroRNA biogenesis impairment leads to precocious expression and propagates the noise of Hoxa5 at the protein level, resulting in an imprecise Hoxa5-Hoxc8 boundary. Here we uncover, using in silico simulation, two feed-forward Hox-miRNA loops accounting for the precocious and noisy Hoxa5 expression, as well as an ill-defined boundary phenotype in Dicer mutants. Finally, we identify mir-27 as a major regulator coordinating the temporal delay and spatial boundary of Hox protein expression. Our results provide a novel trans Hox-miRNA circuit filtering transcription noise and controlling the timing of protein expression to confer robust individual MN identity.
In most bilateral animals, the axial identity along the rostrocaudal (RC) axis of the neural tube is defined by the homeobox (Hox) cluster genes, which encode an array of conserved homeodomain transcription factors. Mutations of these Hox proteins usually lead to homeotic transformation1,2,3. The expression of Hox genes along the RC axis of developing embryos is concordant with its 3′-to-5′ aligned direction within the Hox cluster that is usually referred to as ‘spatial collinearity’ of Hox genes. In addition, Hox genes are activated one after the other sequentially in the 3′-to-5′ direction in a process described as ‘temporal collinearity.’ Although, both spatial and temporal collinearity features are known to be highly conserved across bilaterians, the molecular details and the overall mechanism underlying the coordination of spatiotemporal collinearity of Hox genes is still obscure.
In addition to their well-known function in defining early axial identity, Hox cluster genes play critical roles in neural circuit formation by adopting cell-type specific programs that define the synaptic specificity of neuronal subtypes in the hindbrain and spinal cord4,5,6. The role of RC positional identity in neuronal specification has been carefully examined in the context of spinal motor neuron (MN) development, where there is a clear segregation of MN subtypes targeting specific muscles along the RC axis of the spinal cord. Gradients of retinoic acid (RA), fibroblast growth factor (FGF), and growth differentiation factor 11 (Gdf11) establish initial patterns of Hox gene expression in the early embryos7,8,9. Rostral RA primarily induces Hox1 through Hox5 genes, whereas FGF at the posterior tip induces Hox6 through Hox9 and Gdf11/FGF8 activate Hox10 and Hox11 genes. Hox proteins then interpret the extrinsic signals to define the individual neuronal identity by mutually exclusive expression. Yet, how opposing gradients (RA and FGF) cross-talk and how the spatial or temporal components of morphogen gradients coordinate to set up the precise boundary and neuronal subtype remain enigmatic.
Within Hoxc6on limb-innervating motor neurons (LMC-MNs), mutually exclusive expression between Hox5 and Hoxc8 proteins further establish the boundary between molecularly-defined motor pools. Hox5 proteins (Hoxa5 and Hoxc5) are required to generate the motor pool that expresses the transcription factor Runx1 in the rostral LMC neurons, whereas Hoxc8 is required in the caudal LMC neurons to generate the motor pools that express the transcription factors Pea3 and Scip10,11. Although genetic evidence shows that Hox cluster genes are important to demarcate motor neuron subtype identity and synaptic connectivity, it remains unclear how Hox cluster genes coordinate to robustly define the individual neuronal subtype identity and whether additional critical factors are involved for Hox gene regulation.
In recent years, it has become clear that microRNA (miRNA) embedded within the Hox clusters is important to refine Hox genetic dynamics to ensure axial identity1,12,13,14. For example, miR-10 resides in almost all taxa between Hox4 and 5 paralogs and arose in early bilaterians, while miR-196 is located between Hox9 and 10 paralogs and is specific to vertebrates and urochordates. Genetic knockout or overexpression studies further indicate that Hox-embedded miRNAs are involved in regulating Hox gene expression at the post-transcriptional level15,16,17,18,19. Interestingly, while Hox genes are transcribed in spinal progenitors, many Hox proteins are only detectable in postmitotic MNs7,20. Several Hox transcripts are localized in broader domains than their corresponding proteins21,22, indicating that post-transcriptional regulation is involved in the refinement of the spatiotemporal Hox collinearity features reflected at transcriptional levels in the developing spinal cord. As we and others have demonstrated that miRNAs are critical in dorsoventral progenitor patterning, as well as motor neuron subtype diversification in the spinal cord23,24,25,26,27,28, here we aimed to test whether miRNAs might prevent precocious Hox protein expression until neurons differentiate and whether this regulation is functionally important.
In this study, we first verify that most 3′ Hox transcripts are activated upon RA activation in embryonic stem cell (ESC)-derived neuroepithelia. We find that the Hoxa5 transcript displays robust but noisy transcription at motor neuron progenitors (pMNs), and conditional deletion of the miRNA biogenesis enzyme Dicer in neural progenitors leads to precocious and fluctuated expression of Hoxa5 protein, which results in an imprecise boundary between Hoxa5-Hoxc8 in vitro and in vivo. By taking advantage of in silico simulation of the Hox gene and miRNA network, we find that removing two critical feed-forward Hox-miRNA loops can recapitulate the precocious noisy Hoxa5 expression and rough boundary phenotype of Dicer mutants. Moreover, we identify mir-27 as a major regulator governing temporal and spatial collinearity of Hox protein expression, which emphasizes the emerging role of miRNA in filtering protein expression noise and provides evidence that miRNA confers precision to protein expression, thereby controlling the developmental boundary and individual cell identity.
Hox protein expression lags in spinal pMNs
The pattern of Hox gene expression is established by a rostrocaudal gradient of morphogens and the mutually exclusive expression of Hox proteins in which their cross-repressive interactions further consolidate the individual motor neuron subtype identity5,6. While several Hox genes contain RA response elements within proximal enhancers and have their transcription directly activated by RA signal, many Hox proteins accumulate only in postmitotic MNs7,29. Furthermore, the mechanisms contributing to the time lag between Hox transcription and translation are still unknown. To dissect the significance underlying the delay between Hox transcription and translation, we first profiled global Hox gene expression using an in vitro ESC-derived motor neuron differentiation system (Fig. 1a; Supplementary Fig. 1a). Consistent with previous study29, most of the 3′ Hox genes were robustly induced upon RA treatment within 8 h (differentiation Day2), particularly those from the HoxA and HoxC clusters (Fig. 1b; Supplementary Table 1). As ESC-derived MNs subjected to RA/Smoothened Agonist (SAG) conditions acquired cervical/brachial Hoxa5on identity29,30, we focused on confirming the temporal and spatial expression of the Hoxa5 gene and protein by quantitative real-time PCR (qPCR) and immunostaining. In contrast to the robust induction of Hoxa5 transcription in neuroepithelial embryoid bodies (EBs, Days 3–4), Hoxa5 protein only became detectable in postmitotic MNs (Day5) (Fig. 1c–f). Concomitantly, our in situ hybridization of the Hoxa5 transcripts and immunostaining of Hoxa5 protein on the same cervical spinal section at E12.5 further confirmed the discrepancy between Hoxa5 mRNA and protein expression in the progenitor ventricular zone (Supplementary Fig. 1b).
To reveal if the timing delay was simply a reflection of the sensitivity of the Hoxa5 antibody used in this study, we generated a ‘Tet ON’ iHoxa5 ESC and induced exogenous Hoxa5 mRNA expression with a linear concentration gradient of Dox (doxycycline), as the timing and level of expression of the inducible gene in this ESC can be accurately controlled by Dox (ref. 31) (Supplementary Fig. 2a). We then used qPCR to determine the corresponding Dox dosage for the comparable endogenous Hoxa5 mRNA expression level in ESC-derived Day2 and 5 differentiated EBs. Given that exogenously-induced Hoxa5 did not contain a 3′UTR, we could then systematically test the Hoxa5 mRNA/protein correlation and sensitivity in parallel between exogenous and endogenous Hoxa5 (Supplementary Fig. 2b).
We tested several available Hoxa5 antibodies used in this study10 (Supplementary Fig. 2c and d). We observed robust and early Hoxa5exo protein expression at a low Dox dosage (125 ng ml−1), while the corresponding [Dox] for Hoxa5endo in Day2 EBs did not manifest detectable Hoxa5, as revealed by immunostaining. This result indicates that the Hoxa5 antibodies used in this study have high sensitivity, and the expression timing delay between Hoxa5 mRNA and protein during MN differentiation is attributable to 3′UTR-mediated post-transcriptional repression in vivo. Altogether, we conclude that Hoxa5 has significantly delayed protein expression in the developing spinal cord.
Strong heterogeneous Hoxa5 mRNA expression in pMN
Why does Hoxa5 exhibit significant mRNA expression in the progenitors and execute delayed protein expression until the postmitotic stage? As transcription is relatively noisy in living organisms and stem cells32,33, we tested if Hoxa5 transcription exhibits a strong heterogeneous pattern in the pMNs. To study this, we performed single molecule RNA FISH (smFISH) to visualize Hoxa5 at single-cell resolution. We designed probes to recognize unique Hoxa5 sequences to prevent cross-reaction with the conserved homeodomain region of other Hox genes (Fig. 2a). First, we tested the specificity of smFISH probes in ESC-derived MNs. Compared to a scramble (Scr) control probe that did not show signals, the Hoxa5 probe set manifested strong punctate signals in Hb9::GFPon MNs (Fig. 2b). To further corroborate the in vitro observation, we performed smFISH for Hoxa5 in the spinal cord sections of E9.5 Hb9::GFP embryos. N-cadherin was used to outline the cell margin, whereas Olig2/Sox1 and Hb9::GFP were used to reflect pMNs and post-mitotic MNs on adjacent sections (Fig. 2c). Compared to the relative homogenous expression within postmitotic GFPon MNs, strong cell-to-cell variation of Hoxa5 transcripts in pMNs was observed (Fig. 2d and quantification in 2E, n=5 embryos). These results indicate that Hoxa5 mRNAs exhibit strong cell-to-cell fluctuations in pMNs, so that pMNs might need a noise-filtering machinery to prevent precocious protein expression at this stage.
Dicer−/− causes precocious and noisy Hoxa5 protein expression
Given that several studies have indicated that Hox genes can be either regulated post-transcriptionally17,34,35, we investigated whether miRNAs are required to regulate the timing of Hoxa5 protein expression. We first used conditional Dicer ESCs in which one or both Dicer alleles can be disrupted by 4-hydroxytamoxifen (4-OHT) treatment, and examined if the decreased levels of miRNAs affect the timing of Hoxa5 protein expression (Supplementary Fig. 3a). On Day4 of differentiation, control cells did not manifest Hoxa5 proteins in the EBs, whereas identical treatment of the Dicer−/− ESC resulted in a significant increase in the percentage of progenitors expressing Hoxa5 (n=3 independent experiments; Supplementary Fig. 3b–d). Precocious Hoxa5 protein expression was not attributable to mRNA level, as qPCR revealed comparable Hoxa5 in control and Dicer−/− EBs (Supplementary Fig. 3e).
Notably, the precocious Hoxa5 expression in Dicer−/− EBs exhibited stronger cell-to-cell variability than the controls (Supplementary Fig. 3d). To further verify this phenotype in vivo, we examined the expression patterns of Hox proteins in Sox2-CreTg/+; Dicerfloxed (epiblast deletion at E5.5, referred to as DicerepiblastΔ) embryos. Despite the spina bifida phenotype observed at E8.5 in the DicerepiblastΔ embryos (Supplementary Fig. 4a–d), neural tubes still displayed robust neural patterning markers (Pax6on, Olig2on and Nkx2.2on in Supplementary Fig. 4e and f) and morphogen signalling pathways were unaffected (Shhon and Raldh2on in Supplementary Fig. 4g). However, Hoxa5 protein was precociously expressed in the neural tube of DicerepiblastΔ embryos (Supplementary Fig. 4h). To circumvent the morphogenesis defects of neural progenitors in the DicerepiblastΔ embryos, we alternatively used Sox1Cre/+; Dicerfloxed with a ROSA26-loxp-STOP-loxp YFP reporter (neuroepithelium deletion from E7.5, hereafter referred to as DicerneuralΔ embryos), in which the miRNA biogenesis pathway was only impaired in the central nervous system (Supplementary Fig. 4i and j; Fig. 3a,b). DicerneuralΔ embryos exhibited perinatal lethality and a shortened axis (Supplementary Fig. 4k). We verified that the recombination efficiency of Sox1Cre/+ in the spinal cord is nearly ∼100% (Fig. 3a,b, protein intensity is quantified and shown by heat map in Fig. 3i,j). This is consistent with previously published literature using the same Sox1Cre/+ line, and no mosaic feature of this Cre line was raised36.
Next, we used Sox1/Doublecortin (Dcx) /Isl1(2) staining to demarcate the progenitor (VZ), nascent MNs (VZ–IZ) and postmitotic (IZ–MZ) zones (Fig. 3g,h). Although the intensity of YFPon cells was homogenously distributed in all regions in the spinal cord, Hoxa5 was manifested precociously and a strong fluctuating pattern in the VZ–IZ zone of DicerneuralΔ embryos was observed. Notably, postmitotic Hoxa5on and Hb9on cells displayed a relatively uniform level of expression in the MZ region from control and DicerneuralΔ embryos (Fig. 3c–f, protein intensity reflected by heat map in Fig. 3k–n, and distribution quantification is shown as a histogram in 3O, n=3 embryos). Therefore, these analyses indicate that Hoxa5 displays precocious and fluctuating protein expression in the pMNs of the DicerneuralΔ embryos.
Taken altogether, we suggest that Dicer/miRNA biogenesis places a delay on production of Hoxa5 protein, allowing reduction of Hoxa5 transcription noise. As a result, the impairment of Dicer/miRNA biogenesis leads to precocious propagation of the noisy Hoxa5 protein in pMNs (Fig. 3p).
Dicer deletion results in a distorted Hoxa5/Hoxc8 boundary
As a previous study demonstrated that Hoxa5 and Hoxc8 proteins define the rostrocaudal identity and position of motor pools10, we therefore tested whether the precocious and noisy Hoxa5 protein distribution leads to impairment of the boundary formation of postmitotic MNs. To examine whether the decreased levels of miRNAs affect the Hox boundary, 4-OHT-treated controls and conditional Dicer−/− ESCs were exposed to caudalized medium on Day2 of differentiation (Fig. 4a). On Day7 of differentiation, controls exhibited comparable numbers of mutually-exclusive Hoxa5on and Hoxc8on cells in the EBs, yet Dicer−/− EBs exhibited a significant increase of Hoxa5on motor neurons. More importantly, ∼5–10% of motor neurons manifested co-expression of Hoxa5 and Hoxc8 (n=3 independent experiments; Fig. 4b,c).
To verify this phenotype in vivo, we examined the Hox expression in DicerneuralΔ embryos. While the reciprocal expression of Hoxa5 and Hoxc8 was maintained along the rostrocaudal axis in the Hox6on LMC motor neurons in the control embryos, Hoxa5 was expanded caudally into Hoxc8on territory, with a significant increase of Hoxa5/Hoxc8 co-expressing cells (n=9 embryos in Fig. 4d and quantification in 4e for transverse sections at E12.5).
Altogether, precocious Hoxa5 expression in pMNs leads to a less straight, more ill-defined Hoxa5-Hoxc8 boundary in postmitotic MNs. Dicer−/− mutants displayed strong noisy patterns of Hox5 and Hox8 expression compared to the control, suggesting that miRNA biogenesis plays a critical role in buffering noise (Fig. 4f).
Temporal and spatial modelling for Hox-miRNA interactions
Previous studies have shown that the dynamics of signalling networks is critical for robust formation of boundaries between adjacent domains in developing tissues10,37,38. To map the possible miRNA signalling network in regulating the timing of Hoxa5 protein expression and the robust formation of the Hoxa5/Hoxc8 boundary, we first built a mathematical model of cells expressing Hoxa5 and Hoxc8 in the developing spinal cord. The model describes each cell as a signalling network under the influence of various levels of RA and FGF depending on the position of the cell in the domain. We first built a preliminary network using known interactions in postmitotic MNs5,6. With this network and a set of basal parameters (see Supplementary Table 2 and Method), we incorporated a hypothetical miRNA (mir-x) and sampled parameter sets that represent 324 possible network topologies involving mir-x (Fig. 5a, upper panel). With this spatial model, we scored these topologies based on the robustness and accuracy of the Hoxa5/Hoxc8 boundaries in response to fluctuating morphogen signals (RA and FGF) (see Method). Interestingly, the top-scored topologies had three consensus interactions: (1) inhibition of mir-x by RA, (2) inhibition of Hoxa5 protein expression by mir-x and (3) activation of mir-x by Hoxc8 (Supplementary Fig. 5a and Fig. 5a, lower panel). Simulation with this predicted Hox-miRNA network recapitulated the spatial and temporal dynamics described in previous sections (Fig. 5b,c; Supplementary Fig. 5b). Moreover, the absence of mir-x in the model caused precocious expression of Hoxa5 protein and its rough boundary (Fig. 5b,c). The simulations were also consistent with the Dicer−/− cells that have broader distributions of Hoxa5 protein than WT cells at the early stage of activation (Fig. 5d). This suggests that mir-x is involved in controlling both temporal fluctuations and spatial patterns of gene expression.
We noticed that the predicted Hox-miRNA network involves two coherent feed-forward loops via mir-x (Supplementary Fig. 5c). As this type of motif is known for its role in generating delayed responses and filtering noisy signal input39, we further examined the temporal behaviour of Hoxa5 protein expression in response to RA signal. Consistent with the experimental observations, our simulation showed that the presence of mir-x is essential for the delayed response of Hoxa5 protein (Supplementary Fig. 5d), suggesting a critical role of the coherent feed-forward loop in controlling temporal dynamics of Hoxa5. Since this delay is due to the relatively slow response of the indirect arm of this loop (RA-mir-x-Hoxa5, see Supplementary Fig. 5d), we examined whether accelerated responses via miRNA could cause precocious formation of the Hoxa5-expressing domain and roughness of its boundary. Indeed, the boundary of the Hoxa5-expressing domain became rough when the mir-x-mediated response was accelerated (Fig. 5e). This implies that the robustness of Hoxa5/Hoxc8 spatial patterning is influenced by the temporal dynamics of the miRNA signalling network. This model also suggests that early expression of mir-x occurs in the entire domain and its late expression is restricted to the Hoxc8 expression domain (Fig. 5e).
Hoxa5 activities are modulated by mir-27
To test this model in vivo, we sought to identify which miRNA is responsible for the timing of Hoxa5 expression and refinement of the Hoxa5-Hoxc8 boundary in the spinal cord. We first profiled miRNA during in vitro ESC motor neuron differentiation using the NanoString platform and identified 20 miRNAs steadily downregulated by application of RA/SAG after differentiation (Fig. 6a; Supplementary Table 3). Out of these 20 miRNAs downregulated by RA, only one miRNA, mir-27, was predicted to target the 3′ UTR of Hoxa5 mRNA across vertebrates by the target prediction algorithm TargetScan 6 (Fig. 6a). Independent qPCR analysis (n=3) confirmed that both expressions of mir-27a and mir-27b were gradually downregulated during ESC-derived MN differentiation (Fig. 6b). This is the opposite to the steady increase of Hoxa5 expression during MN differentiation. Therefore, complementary expression of mir-27/Hoxa5 suggests that the delayed expression of Hoxa5 protein could be a reflection of strong mir-27 expression in the pMNs.
As mir-27a/b have the same seed sequence and their expression profiles are similar, we only tested whether mir-27b could be induced by Hoxc8 in MNs. We generated a ‘Tet-ON’ inducible HOXC8 ESC with a V5 tag and induced the expression of HOXC8 in pMN by doxycycline treatment on Day4 of differentiation, which resulted in efficient suppression of Hoxa5 expression (Fig. 6c–e; Supplementary Fig. 6a–e). Concomitantly, expression of mir-27b on Day6 was significantly induced upon HOXC8 induction, whereas ubiquitous mir-16 was not affected in the postmitotic MNs (Fig. 6f, n=3 independent experiments). On the basis of these observations, we elected to examine the function of mir-27 further in regulating the timing of Hoxa5 protein expression and boundary establishment.
Dynamic mir-27 expression along the RC axis of the spinal cord
To verify expression of mir-27b in the developing spinal cord, we performed whole mount in situ hybridization on E8.5 mouse embryos and revealed that mir-27b was highly expressed in all neuroepithelial tissues, yet was gradually caudalized and enriched in the brachial spinal cord at E9.5 (Supplementary Fig. 6f and g). This finding was consistent with our simulation results (Fig. 5e). At E12.5, in situ hybridization along the rostrocaudal axis of the spinal cord indicated that mir-27b was enriched in the caudal brachial (C7-T1) spinal region corresponding to the Hoxc8on domain and was reduced in the rostral Hox5on brachial region (Fig. 6g). To determine whether Hoxa5 is a direct target of mir-27, we constructed a luciferase reporter containing the full length 3′ UTR of Hoxa5 harbouring the three predicted mir-27 target sites (Fig. 6h). We developed a ‘Tet-ON’ inducible ESC line (iMir27b), in which the primary mir-27b sequence was inserted into the 3′UTR of an inducible GFP construct26. Transfection of the luciferase construct with mir-27b overexpression upon doxycycline induction resulted in ∼40% reduction in luciferase activity (Fig. 6i), whereas an Olig2 3′UTR with no mir-27 putative target sites was unaffected. The miRNA target prediction algorithms identified three potential binding sites for mir-27. We therefore mutated the three binding sites simultaneously or individually in Hoxa5 3′UTR reporter constructs (Fig. 6h), and constructs with combinations of two simultaneously-mutated putative mir-27 binding sites were completely insensitive to mir-27-mediated silencing (Fig. 6i).
Taken altogether from the results of iHOXC8 analysis and in situ hybridization in vivo, as well as the luciferase assay, we suggest that mir-27 is induced by Hoxc8 and is targeted to the 3′ UTR of Hoxa5 directly.
Mir-23–27–24 DKO embryos phenocopy DicerneuralΔ embryos
To corroborate the role of mir-27 in preventing Hoxa5 precocious protein expression and maintaining the precise boundary between Hoxa5-Hoxc8, we further examined Hoxa5 protein expression in CRISPR/Cas9-generated mir-23–27–24 cluster double knockout (DKO) ESC-derived MNs40. Compared to wild type controls, Hoxa5 protein was precociously expressed in pMNs of mir-23b–27b–24-1−/−, and even more markedly in DKO, whereas Sox1on cells were unaffected in Day3 progenitors (Fig. 7a–c). We then used the same gRNAs to generate mir-23–27–24 cluster DKO embryos, verified the genotype, and tested the observed phenotype in DicerneuralΔ embryos. In the DKO embryos, we observed profound precocious and fluctuated Hoxa5 expression in the pMNs (E10.5), whereas the expression of Hb9 was unaffected (Fig. 7d–i, protein intensity reflected by heat map in Fig. 7j–m, and distribution quantification is shown as a histogram in Fig. 7n, n=3 embryos). Notably, this phenotype is similar to DicerneuralΔ embryos in Fig. 3. Thus, Hoxa5 displayed precocious and fluctuating protein expression in the pMNs of mir-23–27–24 cluster DKO embryos.
Characterization of mir-27 in ESC–MNs and chicken embryos
To dissect if mir-27 alone in the mir-23–27–24 cluster can lead to the observed phenotype, we developed an iMir27 sponge ESC (iMir27SP), in which eight sequence repeats complementary to miR-27 were inserted into the 3′ UTR of GFP (Fig. 8a)41. To verify the dose requirement for stably saturating miRNA, we induced iMir27SP and a control 8 × repeated scramble sequence sponge (iScrmSP) with different doses of Dox. Both ESCs induced GFP in response to Dox dosages by the TRE promoter. In control iScrmSP cells, the number of positive GFPon cells and the GFP mean fluorescence intensity increased proportionally with Dox concentration (Supplementary Fig. 6h). In iMir27SP ESCs, we observed a significantly lower GFP intensity at lower [Dox] (<500 ng ml−1), indicating that mir-27 was regulating its endogenous targets.
To test whether mir-27SP recapitulated precocious Hoxa5 expression in Dicer−/−pMN cells, we applied 2 μg ml−1 Dox at Day2 of ESC-MN differentiation. We observed that the Hoxa5 protein level increased significantly in pMN cells (Day4) in iMir27SP cells, whereas Hoxa5 was not detected in the control iScrmSP cells (n=3 independent experiments, Fig. 8a–c). The precocious Hoxa5 protein expression in mir-27SP EBs was not a reflection of postmitotic fate, as Olig2on progenitor cells were not affected (Fig. 8c).
To assess the effects of impairing miR-27 activity on the Hox boundary in the embryonic spinal cord, we electroporated mir-27SP vectors into chick neural tubes as mir-27 sequence and its targets sites upon Hoxa5 are conserved in vertebrates (mir-ScrmSP separately as a control; Fig. 8d; Supplementary Fig. 6i). We then monitored the expression levels of GFP 2–3 days after electroporation. While Hoxa5-Hoxc8 segregated sharply in the control mir-ScrmSPelect embryos, we observed a significant increase of co-expressed Hoxa5/Hoxc8 cells in the mir-27SPelect embryos (Fig. 8f and quantification in 8g). The miR-27 loss-of-function condition did not decrease the number of generic Isl1(2)on postmitotic MNs (Fig. 8e), suggesting that the inhibitory effect of miR-27 blockade is specific to the Hox boundary.
Taken altogether with the in ovo, iMir27SP EB, and mir-27 DKO embryo studies, we conclude that mir-27 controls the timing of Hox5 expression to confer the robustness of the Hoxa5-Hoxc8 boundary in the developing spinal cord (Supplementary Fig. 7).
Hox genes are well-known transcriptional regulators that elicit distinct developmental programs to orchestrate positional identities of cells and tissues. Recent studies have further revealed that Hox genes play multifaceted roles in controlling neuronal subtypes to confine synaptic specificity during development5,6. This indicates that Hox gene expression needs to be dynamically controlled at several levels to ensure proper axis formation and to elicit cell diversity in embryos. Here, using in vitro, in silico and in vivo approaches, we tested whether delayed Hoxa5 protein expression is controlled by miRNA and if this phenomenon is important for spatial boundary establishment.
Our results provide insights into the functional significance of the temporal delay in Hox protein expression. Before neural tube closure, morphogens first provide positional information for spatial patterns of gene expression during development. The retinoic acid morphogen signal leads to activation and binding of retinoic acid receptors (RARs) to the Hox1 through Hox5 chromatin domains, followed by a rapid domain-wide removal of H3K27me3 and acquisition of cervical spinal identity29,42. Interestingly, our single molecule FISH revealed that the Hoxa5 transcript fluctuates in the pMNs, indicating that stochastic effects such as local fluctuations in morphogen concentration and noise in signal transduction make it difficult for pMNs to respond to their positional cues with sufficient fidelity to enable sharp boundary formation between gene expression domains37,38,43,44. In future experiments that adopt a single-cell approach to analyse pMNs from embryos, it will be interesting to examine the global Hox pattern at single-cell level and to see if this pattern is a universal phenomenon.
Previous studies have revealed that transcriptome-wide noise controls lineage choices in mammalian stem cells or progenitor cells, and cell-to-cell variability in the progenitors could be important in steering lineage choices of progenitors33,45,46. The slowly fluctuating transcriptome that is distinct from one progenitor cell to the next may govern the reversible, stochastic priming of multipotent progenitor cells in cell fate decisions, consistent with our previous study showing that the early spinal progenitors are malleable. To maintain the plasticity of progenitors, pMNs must act in concert and apply a refinement mechanism to ensure the robust output of motor neuron subtypes in adopting a given postmitotic cell fate in an ‘all-or-none’ manner. Using mouse genetics and systems modelling, we have further shown that delaying the expression of Hox transcripts by miRNA and regulating the spatially and temporally varying gradient of RA signal through RA-Hox-miRNA logic can confer the robustness and reliability of motor neuron subtype diversification. This agrees with emerging evidence emphasizing that miRNA might function to canalize genetic programs, filter transcription noise and confer robustness and accuracy to gene expression. Our results further underscore that the precise timing of Hox gene activation is functionally important because the experimental conditions resulting in premature or delayed Hox gene activation have been shown to produce phenotypic alterations47,48,49,50.
Why do embryos adopt a delayed protein expression system controlled by Hox-miRNA logic? Studies in mouse and fly embryos demonstrate that Hox-regulating miRNAs are encoded within the Hox clusters. This genomic arrangement might provide an effective cis mechanism to ensure the posterior prevalence of Hox genes12. However, the cis embedded miRNAs in the Hox cluster are not expressed in the pMNs, and we therefore ruled out their potential role to regulate the delayed Hox protein expression in our system. Given that several lncRNA have been proven to act in trans to regulate the Hox epigenetic landscape14,51,52, our study here further provides evidence that trans miRNA (mir-27) outside the Hox cluster participates in the Hox network to confine the timing and robustness of Hox gene expression.
Our study has uncovered a novel role of miRNA in the formation of a robust and sharp boundary between two cell types by regulating the timing of Hox expression. Similar to DV progenitors exposed to Shh signals emanating from the notochord, Hox transcripts are induced according to the activity of RA and FGF. At this stage, progenitors responding to RA might still fluctuate, and the expression of Hox mRNA exhibits both temporal and cell-to-cell variability37,43. Translation of fluctuating transcripts at this time would propagate the noise, leading to strong stochastic variability. Due to slow inhibitory dynamics of RA on mir-27, fluctuating RA is unlikely to exert sustained inhibition on mir-27. Therefore, the coexistence of mir-27 with Hox mRNA at this stage can prevent precocious Hoxa5 protein expression. At the nascent postmitotic stage, most MNs turn on Hoxa5 expression more synchronously, and RA signalling stably inhibited mir-27, allowing robust nascent Hoxa5 protein expression. Consequently, Hoxc8 further maintains the expression of mir-27 to generate a coherent feed-forward inhibition pathway to maintain the mutually exclusive Hoxa5-Hoxc8 sharp boundary10. This is similar to our previous study showing Olig2/Irx3/mir-17-3p constitutes a feed-forward circuit to carve the p2/pMN boundary28. We speculate that the relationship between the miRNA-induced protein expression delay and the robust boundary formation could be a general design principle for other miRNA circuits. As cis-embedded Hox miRNAs have been shown to ensure posterior prevalence during embryonic development, it will be equally interesting to see how cis and trans miRNAs together orchestrate Hox activity and provoke neuronal diversity along the RC axis of the spinal cord.
As coherent feed-forward loops are known to cause delayed responses and help to protect the system against brief fluctuations of signals in bacteria53, our mathematical model demonstrates that this network motif is critical for development of mammalian tissues by delaying the cellular response to morphogens, indicating its ubiquitous roles in biological systems. This control mechanism is distinct from the well-known bistable system that also confers robustness against morphogen fluctuations38, or the noise-driven sharpening of the boundary that depends upon bistability43. In the developing spinal cord, several previous studies and our inducible Hoxa5 ESC system revealed that Hoxa5 does not inhibit Hoxc8 (refs 5, 10). However, the expression of Hox transcription factors is generally controlled by selective, cross-repressive interactions that occur both rostrocaudally and within segments of the spinal cord10. As a consequence, minor fluctuations in starting Hox conditions within individual MNs will result in a ‘winner-take-all’ extinction of expression of one or the other of two opponent Hox proteins on a largely stochastic basis. It is unclear whether Hoxa5-Hoxc8 asymmetric interactions might have a certain unexplored evolutionary advantage or some unknown positive feedback to facilitate this stochastic decision. It would be interesting to explore the possibilities in future studies. It is also possible that multiple mechanisms might contribute to the sharpening of the Hoxa5-Hoxc8 boundary. Future studies are warranted to explore the possible existence of positive feedback loops, which are essential to the creation of bistability in this system.
Mouse ES cell culture and differentiation
Hb9::GFP; conditional Dicer floxed, and miR-23–27–24 single and double KO ESCs (gift from Yue Huang, PUMC China) were cultured and differentiated into spinal motor neurons26,54. In some cases, caudal LMC neuron differentiation was acquired by including 100 ng ml−1 bFGF together with reduced concentrations of RA and SAG at Day2 of differentiation28,29.
Commercially available primary antibodies used in this study include: rabbit anti-HOXA5 (1/2,000, Sigma-Aldrich, HPA029319), HOXC5 (1/2,000, Sigma-Aldrich, HPA026794), HOXC8 (1/2,000, Sigma-Aldrich, HPA028911), guinea pig or rabbit anti-Hoxa5 (gifts from J Dasen and TM Jessell, and made in house), Hoxc8, Olig2, Pax6, Raldh2, Nkx2.2, Shh, guinea pig or rabbit anti-Hoxc6 and Hoxc9 (gifts from TM Jessell). Mouse monoclonal anti-Isl1(2), Hb9, and Hoxc8 were purchased from DSHB. Alexa488-, Cy3- and Cy5-conjugated secondary antibodies were obtained from either Invitrogen or Jackson Immunoresearch.
miRNA in situ hybridization
Sections were fixed in 4% paraformaldehyde and acetylated in acetic anhydride/triethanolamine, followed by washes in PBS. Proteinase K treatment was skipped for post-immunostaining. Sections were pre-hybridized in hybridization solution (50% formamide, 5 × SSC, 0.5 mg ml−1 yeast tRNA, 1 × Denhardt’s solution) at room temperature, then hybridized with 3′-DIG or FITC-labeled LNA probes (3 pmol) (LNA miRCURY probe; Exiqon) at 25 °C below the predicted Tm value. After post-hybridization washes in 0.2 × SSC at 55 °C, the in situ hybridization signals were detected using the NBT/BCIP (Roche) or Tyramide Signal Amplification system (Perkin-Elmer) according to the manufacturer’s instructions. Slides were mounted in Aqua-Poly/Mount (Polysciences, Inc) and analysed with a Zeiss LSM510/710 Meta confocal microscope.
Single molecule FISH
Embryos from various developmental stages (E9.5–E10.5) were obtained from timed matings of Hb9::GFP mice, and detection of a mating plug was counted as embryonic day 0.5 (E0.5). Embryos were dissected out, fixed in 4% paraformaldehyde in PBS for 2 h, and balanced in 30% sucrose after several washes. Fixed embryos were then embedded in OCT compound (Tissue-Tek), frozen in dry ice and stored at −80 °C until use. Spinal sections (5–10 μm) were made with a CM 1950 cryostat (Leica) and immediately placed on slides. For RNA FISH, sections on slides and cultured cells on coverslips were refixed in 4% paraformaldehyde for 10 min at room temperature, permeabilized for 5 min on ice in PBS with 0.5% Triton X-100, then rinsed in 70% EtOH for subsequent RNA FISH. Slides and coverslips were kept in 70% EtOH at 4 °C until staining. Sections were then washed in wash buffer (10% deionized formamide in 2 × SSC) for 5 min and incubated in a dark room at 37 °C for at least 4 h with 1 μl of probe stock solution and 100 μl of hybridization buffer (1 g dextran sulfate, 1 ml 20 × SSC, 1 ml deionized formamide). Hoxa5 and control smFISH probes were purchased from Stellaris. Images were captured with a Delta Vision microscopy system and quantified by Image J. N-cadherin was used to outline the cell margins; Olig2 and Hb9 were used to reflect pMNs and postmitotic MNs. The coefficient of variation was calculated from motor neuron progenitor and postmitotic Hb9::GFPon regions from five embryos.
Mouse crosses and in vivo studies
Conditional neural epithelium-knockout mice were generated by crossing Sox1Cre/+ mice36 (a kind gift from Shin-Ichi Nishikawa in RIKEN CDB) or Sox2::Cre (ref. 55) mice with Dicerloxp/loxp (ref. 56) to generate the Sox1Cre/+; Dicerloxp/WT strain. Sox1Cre/+; Dicerloxp/WT mice were then mated with Dicerloxp/loxp for experimental analysis. miR-23–27–24 single and double KO embryos were made by a CRISPR-Cas9 mediated approach (IMB transgenic core). These mice were backcrossed to mice with a C57BL/6 background for eight generations before use. Mice were mated at age of 8–12 weeks and the embryo stage was estimated as E0.5 when copulation plug was observed. Embryos were analysed between E8.5 and 13.5. All of the live animals were kept in an SPF animal facility, approved and overseen by IACUC Academia Sinica.
Analysis of Hoxa5 expression in Dicer mutants
The expression of Hoxa5 in control and Dicer mutants was imaged using a confocal system. The intensity of Hoxa5 protein was analysed by MetaXpress (Multi Wavelength Cell Scoring module, MWCS). The MWCS module can be used to analyse cells imaged in 1–7 wavelengths. Immunostaining of Sox1/Doublecortin (Dcx) /Isl1(2) were used to demarcate the progenitor (VZ), nascent MNs (VZ−IZ) and postmitotic (IZ–MZ) zone. We set up four individual wavelengths for DAPI, YFP, Hb9 and/or Hoxa5 staining, thereby getting DAPIon and YFPon cells; DAPIon and Hb9on cells; DAPIon and Hoxa5on cells. The results were quantified by YFP, Hb9, Hoxa5 pixel intensity for cells in VZ, VZ–IZ and IZ–MZ regions. The pixel intensities were plotted as histogram distributions (N=3 embryos from controls or KOs).
To define the threshold, we used the following formula:
Whole cell signal=sum of the intensity of the pixels for one cell.
Background signal=average signal per pixel outside of the spinal cord.
Whole cell signal corrected=Whole cell signal-Background signal.
Integrated Morphometry Analysis (IMA) representations were performed using the Metamorph Software. Briefly, for each IMA, we used 8 colour hues with 32 intensities ranked from maximum (red) to minimum (blue). The maximum and minimum values were calibrated and are indicated on each figure. The colour intensities displayed for each hue were determined automatically by the software and are reflected by histogram.
Quantitative real time PCR
ESCs or embryoid bodies were harvested for total RNA isolation by the mirVana kit (Ambion). For mRNA analysis, 20 ng of total RNA from each sample was reverse transcribed with Superscript III (Invitrogen). One-tenth of the reverse transcription reaction was used for subsequent qRT-PCRs, which were performed in duplicate with at least three independent experimental samples on a LightCycler480 Real Time PCR instrument (Roche) using SYBR Green PCR mix (Roche) for each gene of interest and Gapdh was used as a control for normalization.
For miRNA analysis, 20 ng of total RNA was reverse transcribed with a miRNA-specific primer from TaqMan MicroRNA Assays (Life Technology). A ubiquitous small nucleolar RNA, sno202 or sno234, was used as the endogenous control. Each qRT-PCR was performed in duplicate or triplicate per sample with at least three different experimental samples.
Generation of inducible ‘Tet-ON’ ESCs
Human HOXC8 and mouse Hoxa5 cDNAs were directionally inserted into pENTR/D-TOPO vector (Life Technology) following manufacturer instructions. Primary miRNA sequence or repetitive miRNA sponge sequence was synthesized and cloned into the 3′UTR of p2Lox-GFP. Inducible lines were generated by treating the recipient ESCs for 16 h with Dox to induce Cre, followed by electroporation of p2Lox-HOXC8:V5/Hoxa5/miRNA OE/miRNA SP plasmids. After G418 selection, individual resistant clones were picked and characterized. After 10–15 days of selection, clones were expanded. Details of primer and miRNA sequences are listed in Supplementary Table 4.
Inducible miRNA overexpression and sponge ESCs were cloned into the 3′UTR of the p2Lox-GFP construct, and the same procedure as described above was followed to generate stable ESC clones.
Luciferase reporter assay
Hoxa5 3′ UTRs were individually cloned into the psiCHECK-2 vector (Promega). iMir-27OE or iMir-27SP cells were plated at a density of 8 × 103 per well (96-well plate), expanded for 20 h and transfected with 150 ng of reporter plasmids using 0.8 μl PLUS Reagent and 0.4 μl Lipofectamine LTX Reagent (Life Technology). Cells were lysed 24 h later and processed for luciferase assay using the Dual-Luciferase Reporter Assay System (Promega). Luciferase activity was measured using the Enspire Multimode Plate Reader (Perkin Elmer).
In ovo electroporation
Neural tube electroporation of microRNA sponge constructs was performed on stage 10–15 (HH10–15) chick embryos. For misexpression of mir-sponge to decoy endogenous mir-27 activity, plasmids were titrated (typically 1–4 μg μl−1 CMV-GFP vector). Electroporation efficiency was assayed by GFP expression in the spinal cord. In each experiment, ∼50 embryos were electroporated, with a survival efficiency of ∼20%, such that each set of results reflects an analysis of ∼10 manipulated embryos. Electroporation efficiencies in individual embryos ranged from 30 to 80% of LMC neurons at the segmental level under analysis, and we report results derived from embryos with >50% efficiency.
Statistical analysis was performed using Student’s t test as all quantifications in the control and experimental sets are in similar sample sizes. All experiments were performed in parallel with both experimental and control genotypes. Error bars indicate s.d.
Framework of mathematical model
To describe the system mathematically, we used a generic form of ordinary differential equations (ODEs) suitable for describing both gene expression and molecular interaction networks57,58. Each ODE system in the model has the form:
Here, Xi is the activity or concentration of protein i. On a time scale=1/γi, Xi (t) relaxes toward a value determined by the sigmoidal function, F, which has a steepness set by σ. The basal value of F, in the absence of any influencing factors, is determined by . The coefficients ωj→i determine the influence of protein j on protein i. N is the total number of proteins in the network. All variables and parameters are dimensionless. One time unit in the simulations corresponds to ∼1 day.
To model spatial distribution of proteins and RNAs during development, we considered a series of cells in a one-dimensional domain, representing the rostral-caudal axis of the embryo. These cells are under influence of varying strengths of RA and FGF determined by:
Where Mi,j is the strength of morphogen i at position j. is the strength of morphogen i at the boundary of the domain where the morphogen is synthesized. Dj is the diffusion rate of the morphogen. ki is the degradation rate of the morphogen. xj is the distance between position j and the boundary. This approximates a reaction diffusion system for RA and FGF at steady state. In each simulation, we first ran the system to steady state without morphogen signals, and then we raised the morphogen strengths to particular values and continued the simulation. To consider temporal noise in the RA and FGF gradients, the values of RA and FGF are subject to random multiplicative perturbations during the simulation59. The perturbations of these parameters were introduced in each 1/ω time interval, where ω is the frequency of the noise (ω=10 day−1). In each time interval, random parameters were chosen for the morphogens in ranges proportional to their mean concentrations specified at the beginning of simulations.
Robustness and accuracy of boundary formation
To evaluate the robustness of the Hoxa5/Hoxc8 boundary, we ran multiple simulations for the one-dimensional system and aligned them to create a two-dimensional space. Due to the noisy morphogen signals, the boundary between Hoxa5-expressing cells (defined as a cell expressing >0.5 unit of Hoxa5 protein) and Hoxc8-expressing cells were not always sharp. We defined the ‘transition zone’ of a protein as the domain in which the percentages of cells expressing that protein at a particular horizontal position are between 15 and 85%, and we defined ‘transition width’ (Ω) as the width of the transition zone. We assumed that the expression boundary with respect to the protein is at the midpoint of the transition zone. To evaluate the accuracy of the boundary position in terms of two proteins, we measured the distance between two expression boundaries.
To search for a plausible signalling network controlling Hoxa5/Hoxc8 boundary formation, we first built a basal model without miRNA (Fig. 4a). The interactions of the basal model were based on previously-reported experimental data10. The parameter values of the model were chosen such that the model was able to reproduce the observed overlapping expression of Hoxa5 and Hoxc8 in the absence of miRNA (Fig. 3a). We considered six possible interactions involving a hypothetical miRNA named mir-x (Fig. 4a). We assumed that miRNA mainly inhibits the translational activity of its target mRNA. Therefore, each possible interaction can be quantified by a coefficient ωj→i which can adopt two (for miRNA) or three (for protein) representative values: ωj→i=0, −1 or 1, where 0 means no interaction, −1 means inhibition and 1 means activation. This gave rise to 324 possible network topologies in total. We ran simulations with these topologies and ranked them based on the following metric:
Where, Ωa5 is the transition width of Hoxa5. Ωa8 is the transition width of Hoxc8. Δa5−c8 is the distance between the Hoxa5 expression boundary and the Hoxc8 expression boundary. A low score represents a robust Hoxa5/Hoxc8 boundary. We identified three consensus interactions based on the top 2% of topologies (Supplementary Fig. 5a). We built a mathematical model for mir-x based on these interactions (Fig. 4a). We tested these interactions experimentally in subsequent experiments. The parameter values of the basal and mir-x network are listed in Supplementary Table 2. To exclude the possibility that the search results were sensitive to the interaction strength, we repeated this procedure six times with different strengths of ωj→i in a range of 0.2–1.2. The topology with the best performance was robust to the choice of interaction strength in the range of 0.4–1.2. Nonetheless, we cannot exclude the possibility that other network topologies may satisfy the constraints we imposed in this study.
Simulation of mutant cells/embryo
When simulating Dicer−/−cells, we set the basal rate of mir-x production to be −100. When simulating cells with fast mir-x regulation, we set the relaxation rate of mir-x to be ten times its normal rate.
Gene expression microarray data during ESC-derived MN differentiation have been deposited in the Gene Expression Omnibus under accession code GSE91080, as well as being summarized in Supplementary Table 1. NanoString miRNA microarray expression data is included in this published article (Supplementary Table 3). The authors declare that all data supporting the findings of this study are available within the article and its Supplementary Information files or from the corresponding author upon reasonable request.
How to cite this article: Li, C.-J. et al. MicroRNA filters Hox temporal transcription noise to confer boundary formation in the spinal cord. Nat. Commun. 8, 14685 doi: 10.1038/ncomms14685 (2017).
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Mallo, M. & Alonso, C. R. The regulation of Hox gene expression during animal development. Development 140, 3951–3963 (2013).
Parker, H. J., Bronner, M. E. & Krumlauf, R. The vertebrate Hox gene regulatory network for hindbrain segmentation: evolution and diversification: Coupling of a Hox gene regulatory network to hindbrain segmentation is an ancient trait originating at the base of vertebrates. Bioessays 38, 526–538 (2016).
Pearson, J. C., Lemons, D. & McGinnis, W. Modulating Hox gene functions during animal body patterning. Nat. Rev. Genet. 6, 893–904 (2005).
Alexander, T., Nolte, C. & Krumlauf, R. Hox genes and segmentation of the hindbrain and axial skeleton. Annu. Rev. Cell. Dev. Biol. 25, 431–456 (2009).
Philippidou, P. & Dasen, J. S. Hox genes: choreographers in neural development, architects of circuit organization. Neuron 80, 12–34 (2013).
Dasen, J. S. & Jessell, T. M. Hox networks and the origins of motor neuron diversity. Curr. Top. Dev. Biol. 88, 169–200 (2009).
Dasen, J. S., Liu, J. P. & Jessell, T. M. Motor neuron columnar fate imposed by sequential phases of Hox-c activity. Nature 425, 926–933 (2003).
Liu, J. P., Laufer, E. & Jessell, T. M. Assigning the positional identity of spinal motor neurons: rostrocaudal patterning of Hox-c expression by FGFs, Gdf11, and retinoids. Neuron 32, 997–1012 (2001).
Denans, N., Iimura, T. & Pourquie, O. Hox genes control vertebrate body elongation by collinear Wnt repression. eLife 4, e04379 (2015).
Dasen, J. S., Tice, B. C., Brenner-Morton, S. & Jessell, T. M. A Hox regulatory network establishes motor neuron pool identity and target-muscle connectivity. Cell 123, 477–491 (2005).
Lacombe, J. et al. Genetic and functional modularity of Hox activities in the specification of limb-innervating motor neurons. PLoS Genet. 9, e1003184 (2013).
Yekta, S., Tabin, C. J. & Bartel, D. P. MicroRNAs in the Hox network: an apparent link to posterior prevalence. Nat. Rev. Genet. 9, 789–796 (2008).
Mansfield, J. H. & McGlinn, E. Evolution, expression, and developmental function of Hox-embedded miRNAs. Curr. Top. Dev. Biol. 99, 31–57 (2012).
De Kumar, B. & Krumlauf, R. HOXs and lincRNAs: two sides of the same coin. Sci. Adv. 2, e1501402 (2016).
Woltering, J. M. & Durston, A. J. MiR-10 represses HoxB1a and HoxB3a in zebrafish. PLoS ONE 3, e1396 (2008).
Hornstein, E. et al. The microRNA miR-196 acts upstream of Hoxb8 and Shh in limb development. Nature 438, 671–674 (2005).
Yekta, S., Shih, I. H. & Bartel, D. P. MicroRNA-directed cleavage of HOXB8 mRNA. Science 304, 594–596 (2004).
Thomsen, S., Azzam, G., Kaschula, R., Williams, L. S. & Alonso, C. R. Developmental RNA processing of 3'UTRs in Hox mRNAs as a context-dependent mechanism modulating visibility to microRNAs. Development 137, 2951–2960 (2010).
Wong, S. F. et al. Independent regulation of vertebral number and vertebral identity by microRNA-196 paralogs. Proc. Natl Acad. Sci. USA 112, E4884–E4893 (2015).
Joksimovic, M., Jeannotte, L. & Tuggle, C. K. Dynamic expression of murine HOXA5 protein in the central nervous system. Gene Exp. Patterns 5, 792–800 (2005).
Brend, T., Gilthorpe, J., Summerbell, D. & Rigby, P. W. Multiple levels of transcriptional and post-transcriptional regulation are required to define the domain of Hoxb4 expression. Development 130, 2717–2728 (2003).
Coulombe, Y. et al. Multiple promoters and alternative splicing: Hoxa5 transcriptional complexity in the mouse embryo. PLoS ONE 5, e10600 (2010).
Chen, J. A. & Wichterle, H. Apoptosis of limb innervating motor neurons and erosion of motor pool identity upon lineage specific dicer inactivation. Front. Neurosci. 6, 69 (2012).
Luxenhofer, G. et al. MicroRNA-9 promotes the switch from early-born to late-born motor neuron populations by regulating Onecut transcription factor expression. Dev. Biol. 386, 358–370 (2014).
Otaegi, G., Pollock, A., Hong, J. & Sun, T. MicroRNA miR-9 modifies motor neuron columns by a tuning regulation of FoxP1 levels in developing spinal cords. J. Neurosci. 31, 809–818 (2011).
Chen, J. A. et al. Mir-17-3p controls spinal neural progenitor patterning by regulating Olig2/Irx3 cross-repressive loop. Neuron 69, 721–735 (2011).
Asli, N. S. & Kessel, M. Spatiotemporally restricted regulation of generic motor neuron programs by miR-196-mediated repression of Hoxb8. Dev. Biol. 344, 857–868 (2010).
Tung, Y. T. et al. Mir-17 ∼92 governs motor neuron subtype survival by mediating nuclear PTEN. Cell Rep. 11, 1305–1318 (2015).
Mazzoni, E. O. et al. Saltatory remodeling of Hox chromatin in response to rostrocaudal patterning signals. Nat. Neurosci. 16, 1191–1198 (2013).
Peljto, M., Dasen, J. S., Mazzoni, E. O., Jessell, T. M. & Wichterle, H. Functional diversity of ESC-derived motor neuron subtypes revealed through intraspinal transplantation. Cell Stem Cell 7, 355–366 (2010).
Iacovino, M. et al. Inducible cassette exchange: a rapid and efficient system enabling conditional gene expression in embryonic stem and primary cells. Stem Cells 29, 1580–1588 (2011).
Raj, A., Peskin, C. S., Tranchina, D., Vargas, D. Y. & Tyagi, S. Stochastic mRNA synthesis in mammalian cells. PLoS Biol. 4, e309 (2006).
Chang, H. H., Hemberg, M., Barahona, M., Ingber, D. E. & Huang, S. Transcriptome-wide noise controls lineage choice in mammalian progenitor cells. Nature 453, 544–547 (2008).
McGlinn, E. et al. In ovo application of antagomiRs indicates a role for miR-196 in patterning the chick axial skeleton through Hox gene regulation. Proc. Natl Acad. Sci. USA 106, 18610–18615 (2009).
Kondrashov, N. et al. Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning. Cell 145, 383–397 (2011).
Takashima, Y. et al. Neuroepithelial cells supply an initial transient wave of MSC differentiation. Cell 129, 1377–1388 (2007).
Schilling, T. F., Nie, Q. & Lander, A. D. Dynamics and precision in retinoic acid morphogen gradients. Curr. Opin. Genet. Dev. 22, 562–569 (2012).
Balaskas, N. et al. Gene regulatory logic for reading the Sonic Hedgehog signaling gradient in the vertebrate neural tube. Cell 148, 273–284 (2012).
Rosenfeld, N. & Alon, U. Response delays and the structure of transcription networks. J. Mol. Biol. 329, 645–654 (2003).
Ma, Y. et al. Functional screen reveals essential roles of miR-27a/24 in differentiation of embryonic stem cells. EMBO J. 34, 361–378 (2015).
Ebert, M. S., Neilson, J. R. & Sharp, P. A. MicroRNA sponges: competitive inhibitors of small RNAs in mammalian cells. Nat. Methods. 4, 721–726 (2007).
De Kumar, B. et al. Analysis of dynamic changes in retinoid-induced transcription and epigenetic profiles of murine Hox clusters in ES cells. Genome Res. 25, 1229–1243 (2015).
Zhang, L. et al. Noise drives sharpening of gene expression boundaries in the zebrafish hindbrain. Mol. Syst. Biol. 8, 613 (2012).
Cohen, M., Page, K. M., Perez-Carrasco, R., Barnes, C. P. & Briscoe, J. A theoretical framework for the regulation of Shh morphogen-controlled gene expression. Development 141, 3868–3878 (2014).
Trapnell, C. et al. The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells. Nat. Biotechnol. 32, 381–386 (2014).
Abranches, E. et al. Stochastic NANOG fluctuations allow mouse embryonic stem cells to explore pluripotency. Development 141, 2770–2779 (2014).
Zakany, J., Gerard, M., Favier, B. & Duboule, D. Deletion of a HoxD enhancer induces transcriptional heterochrony leading to transposition of the sacrum. EMBO J. 16, 4393–4402 (1997).
Juan, A. H. & Ruddle, F. H. Enhancer timing of Hox gene expression: deletion of the endogenous Hoxc8 early enhancer. Development 130, 4823–4834 (2003).
Gerard, M., Zakany, J. & Duboule, D. Interspecies exchange of a Hoxd enhancer in vivo induces premature transcription and anterior shift of the sacrum. Dev. Biol. 190, 32–40 (1997).
Kondo, T. & Duboule, D. Breaking colinearity in the mouse HoxD complex. Cell 97, 407–417 (1999).
Rinn, J. L. et al. Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs. Cell 129, 1311–1323 (2007).
Dasen, J. S. Long noncoding RNAs in development: solidifying the Lncs to Hox gene regulation. Cell Rep. 5, 1–2 (2013).
Kalir, S., Mangan, S. & Alon, U. A coherent feed-forward loop with a SUM input function prolongs flagella expression in Escherichia coli. Mol. Syst. Biol. 1, 2005 0006 (2005).
Wichterle, H., Lieberam, I., Porter, J. A. & Jessell, T. M. Directed differentiation of embryonic stem cells into motor neurons. Cell 110, 385–397 (2002).
Hayashi, S., Tenzen, T. & McMahon, A. P. Maternal inheritance of Cre activity in a Sox2Cre deleter strain. Genesis 37, 51–53 (2003).
Harfe, B. D., McManus, M. T., Mansfield, J. H., Hornstein, E. & Tabin, C. J. The RNaseIII enzyme Dicer is required for morphogenesis but not patterning of the vertebrate limb. Proc. Natl Acad. Sci. USA 102, 10898–10903 (2005).
Hong, T., Xing, J., Li, L. & Tyson, J. J. A simple theoretical framework for understanding heterogeneous differentiation of CD4+ T cells. BMC Syst. Biol. 6, 66 (2012).
Mjolsness, E., Sharp, D. H. & Reinitz, J. A connectionist model of development. J. Theoret. Biol. 152, 429–453 (1991).
Chen, M., Wang, L., Liu, C. C. & Nie, Q. Noise attenuation in the ON and OFF states of biological switches. ACS Synth. Biol. 2, 587–593 (2013).
We thank the Genomic Core, FACS and Imaging core facilities in IMB for considerable technical help. The Sox1Cre/+ line was a kind gift from Shin-Ichi Nishikawa in RIKEN CDB. We thank J. Dasen (NYU) for providing the gift of Hoxa5 antibody, and Yue Huang (PUMC China) for giving us mir-23–27–24 KO and DKO ESCs. We acknowledge T.-J. Kao from TMU for invaluable technical advice for in ovo experiments. We also acknowledge J.-K. Yu, Y.-H. Su and S.-J. Chou (ICOB, Academia Sinica) for discussing the experimental results, and the IMB Scientific English Editing Core for further reviewing the manuscript. J.-A. Chen is supported by Academia Sinica and MoST, and C.-J. Li is supported by a TIGP-MCB scholarship. This work is funded by Academia Sinica (AS-104-TP-B09), MoST (101-2314-B-001 -004 -MY3) and NHRI (NHRI-EX103-10315NC). Q. Nie was supported by National Institutes of Health grants R01GM107264, R01ED023050 and P50GM76516 and the National Science Foundation grants DMS1161621 and DMS1562176.
The authors declare no competing financial interests.
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Li, CJ., Hong, T., Tung, YT. et al. MicroRNA filters Hox temporal transcription noise to confer boundary formation in the spinal cord. Nat Commun 8, 14685 (2017). https://doi.org/10.1038/ncomms14685
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