We identify SMARCD2 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily D, member 2), also known as BAF60b (BRG1/Brahma-associated factor 60b), as a critical regulator of myeloid differentiation in humans, mice, and zebrafish. Studying patients from three unrelated pedigrees characterized by neutropenia, specific granule deficiency, myelodysplasia with excess of blast cells, and various developmental aberrations, we identified three homozygous loss-of-function mutations in SMARCD2. Using mice and zebrafish as model systems, we showed that SMARCD2 controls early steps in the differentiation of myeloid–erythroid progenitor cells. In vitro, SMARCD2 interacts with the transcription factor CEBPɛ and controls expression of neutrophil proteins stored in specific granules. Defective expression of SMARCD2 leads to transcriptional and chromatin changes in acute myeloid leukemia (AML) human promyelocytic cells. In summary, SMARCD2 is a key factor controlling myelopoiesis and is a potential tumor suppressor in leukemia.
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We thank all medical and laboratory staff members involved in taking care of patients and performing scientific experiments, in particular R. Conca (FACS sorting), J. Hinke (genomic facility), and P. Robinson and S. Mundlos for next-generation sequencing expertise. We thank S. Hollizeck, D. Kotlarz, M. Lyszkiewicz, and N. Zietara for critical scientific discussion. We thank B. Zeller, R. Abdennour, and H. Nordgarden for clinical care of patients and A. Tierens for initial FACS and histological workup. We thank J. Lessard (IRIC, Université de Montréal) for providing antibodies to SMARCD1, SMARCD2, and SMARCD3 and for critical discussion.
The study has been supported by the European Research Council (ERC Advanced Grant 'Explore'), the Else Kröner-Fresenius-Stiftung, the DZIF (German Center for Infection Research), the Deutsche Forschungsgemeinschaft (Gottfried Wilhelm Leibniz Program), the German PID-NET (BMBF), and the Care-for-Rare Foundation.
V.P. was supported by a Monash International Postgraduate Research Scholarship (MIPRS) and a Monash Graduate Scholarship (MGS). G.L. was supported by the NHMRC (1069284, 1044754). The Australian Regenerative Medicine Institute (ARMI) is supported by grants from the State Government of Victoria and the Australian Government. This research was supported in part by the Intramural Research Program of the US National Institutes of Health, NLM. W.E. and C.Z. were supported by the Deutsche Forschungsgemeinschaft (DFG) through LMUexcellent and SFB1243 (subproject A14). J.G. was supported by the Bundesministerium für Bildung und Forschung, Juniorverbund in der Sytemmedizin 'mitOmics' grant FKZ 01ZX1405A, and C.M. is supported by EU Horizon2020 Collaborative Research Project SOUND (633974).
The authors declare no competing financial interests.
Integrated supplementary information
(a–d) Phenotype of patient AII.1. (a,b) Low-set, posteriorly rotated, simple ears, with prominent concha and broad incisura intertragica. (c) Hallux valgus (filled arrowhead) and plantar hyperkeratosis of left foot (empty arrowhead). (d) Sandal gap/increased interdigital space D1–D2 (asterisk) and dorsal feet hyperkeratosis D1 (filled arrowhead). (e–l) Phenotype of patient BII.1. (e,f) Thin hair, ear with dysplastic helix, neck with buffalo hump, and acanthosis nigricans. (g) Misaligned, dysplastic teeth, incomplete amelogenesis imperfecta (filled arrowhead), and accessory teeth in gingival plicae (empty arrowheads). (h,i) Features of metabolic syndrome and pubertas praecox vera, (j) Brachytelephalangy, longitudinal ridges on finger nails, and keratosis pilaris on forearm. (k) Bulging of right humerus diaphysis (empty arrowhead) and osteochondroma (filled arrowhead). (l) Increased interdigital space D1–D2 (asterisk), dorsal feet hyperkeratosis D1, D2 left (filled arrowhead), brittle (5th) nail (empty arrowhead), and pes planus. Images have been partially cropped.
(a–f) HE staining of bone marrow biopsies. (a,d) In 04/2008, HE-stained sections show altered bone marrow microarchitecture with reversion of the myeloid/erythroid ratio and dysplastic megakaryocytes. (b,e) In 10/2008, HE-stained sections show a dysplastic bone marrow with marked fibrosis (filled arrowheads). (c,f) In 04/2011, HE-stained sections show a hypercellular bone marrow with focal and peritrabecular infiltration by blast cells (asterisks). (g–i) Glycophorin C staining of bone marrow sections. (g) In 04/2008, irregular erythroid islands were observed. (h) In 10/2008, abnormal erythroid islands located along fibrotic strands were noted. (i) In 04/2011, erythroid islands are present in the immediate vicinity of blast cells (asterisk). (j–l) CD61 staining of bone marrow sections. (j) In 04/2008, small dysplastic megakaryocytes with hypolobated nuclei were observed. (k) In 10/2008, dysplastic micromegakaryocytes were noted. (l) In 04/2011, hypolobated dysplastic megakaryocytes in differing intensities, reminiscent of inadequate megakaryocyte maturation and megakaryocyte dysplasia, were detected. Images have been partially cropped. Scale bars, approximately 20 μm.
Supplementary Figure 3 Decreased expression of granulocyte-specific proteins in SMARCD2-deficient hematopoietic cells.
(a) Immunohistochemical detection of lactoferrin (LTF) in healthy donor (HD) bone marrow cells showing strong expression of LTF in myeloid cells. (b) Immunohistochemical detection of CD15 on healthy donor bone marrow, showing strong expression of CD15 by mature neutrophilic cells. (c) Immunohistochemical detection of myeloperoxidase showing normal amounts and distribution of myeloperoxidase (MPO)-expressing neutrophilic cells presenting at all stages of maturation. (d) Immunohistochemical detection of LTF in patient AII.1 showing lack of LTF-expressing cells. (e) Immunohistochemical detection of CD15 in patient AII.1 showing reduced intensity and decreased cell numbers of CD15-expressing cells. (f) Immunohistochemical detection of MPO in patient AII.1 bone marrow cells showing a hypercellular bone marrow with presence of neutrophilic cells and blast cells expressing MPO with considerably lower intensity as compared to HD. (g) Immunohistochemical detection of LTF in patient BII.2 shows false positive background staining in a postmortem sample (note that LTF deficiency in cells from BII.1 has previously been documented by ELISA). (h) Immunohistochemical detection of CD15 on patient BII.2 bone marrow cells shows a hypercellular bone marrow with almost complete absence of CD15-expressing cells. (i) Immunohistochemical detection of MPO in patient BII.2 bone marrow cells shows hypercellularity. MPO-positive neutrophilic cells are reduced in numbers and intensity in comparison to HD. (j) Immunohistochemical detection of LTF in patient CII.1 showing a hypercellular bone marrow and a lack of LTF-expressing cells. (k) Immunohistochemical detection of CD15 in patient CII.1 showing a hypercellular bone marrow with markedly reduced intensity and decreased cell numbers of CD15-expressing cells in comparison to HD. (l) Immunohistochemical detection of MPO in patient CII.1 bone marrow cells shows a hypercellular bone marrow with clusters of neutrophilic cells and blast cells. MPO expression is reduced. Images have been partially cropped. Scale bars, approximately 20 μm.
(a) Knockdown of smarcd2 by the splice-blocking morpholino oligonucleotides was examined by RT–PCR. Morpholino SB2 (MO SB2) failed to disrupt smarcd2 splicing. Top, amplification of smarcd2 exon boundaries; bottom, β-actin control; (+) and (–) indicate samples prepared with and without reverse transcriptase, i.e., monitoring for genomic DNA contamination. Image cropped from one gel. The full-length gel image is shown in Supplementary Data 3b. (b) Fluorescence image of Danio rerio strain Tg(mpx:EGFP)i114, control versus smarcd2-morphant embryo. Reduced numbers of GFP-expressing neutrophils are observed in morphant versus control fish embryos. Acquired images: CTRL (n = 15 images), ATG MO (n = 15 images), SB1 MO (n = 15 images) and SB2 MO (n = 15 images). (c) Comprehensive analysis of neutrophil numbers in Tg(mpx:EGFP)i114 at 72 h.p.f. after injection of morpholino oligonucleotides (nonspecific control versus translation-start-site blocker (ATG) and splice-site blocker (SB1 and SB2) MOs against smarcd2. Numbers represent fluorescence-labeled neutrophils per individual fish embryos. Data were pooled from two independent morpholino experiments: CTRL n = 15, ATG n = 15, SB1 n = 15, SB2 n = 15 fish. Center value, mean; error bars, s.d. P values were calculated by two-tailed unpaired t test. Replicates: 2. Please compare to Supplementary Tables 19 and 20. These results are an independent verification of the data in Figure 3b in another neutrophil reporter line. (d) Sanger chromatogram of the CRISPR/Cas9-edited frameshift allele smarcd21/1 (1/1) versus the smarcd2 wild-type allele (wt) indicating the induced mutation c.66dup (Mut).
(a) Erythrocyte staining in zebrafish larvae using O-dianisidine staining. Zebrafish treated with smarcd2 SB morpholino (right) show staining equal to that of control-treated zebrafish (left). Gross comparison shows equal O-dianisidine staining in control and morphant fish. (b) Macrophage numbers in zebrafish treated with smarcd2 SB morpholino and control-treated zebrafish are visualized by mCherry-positive cells in the tail. The smarcd2 SB morpholino, inducing aberrant splicing and consequent smarcd2 deficiency, shows no effect on macrophage numbers. Center value, mean; error bars, s.e.m. P values were calculated by two-tailed unpaired t test. Acquired images: CTRL (n = 94 images) and SB1 MO (n = 48 images). (c) Thrombocyte numbers in zebrafish treated with smarcd2 SB morpholino and control-treated zebrafish are visualized by EGFP-positive cells in the tail. The smarcd2 SB morpholino, inducing aberrant splicing and consequent smarcd2 deficiency, shows no effect on thrombocyte numbers. Center value, mean; error bars, s.e.m. P values were calculated by two-tailed unpaired t test. Acquired images: CTRL (n = 48 images) and SB1 MO (n = 63 images). Data are pooled from two independent experiments in b and c. Replicates: 2, See Supplementary Table 20 for raw data.
(a) FACS sorting strategy of zebrafish neutrophils. (b) Developmental stages of zebrafish granulopoiesis (May–Grünwald Giemsa staining). (c) May–Grünwald Giemsa staining of sorted neutrophils in control versus morpholino knockdown zebrafish. (d) No gross histological differences were recognized nor was any overt difference revealed by a four-category differential count of the embryonic neutrophil population (n = 1 experiment, pooling of neutrophils from n = 150 embryos/group); see Supplementary Table 20 for raw data.
(a) Mouse Smarcd2 (ENSMUST00000021052)-mutant embryonic stem cells (ES cells with heterozygous deletion of Smarcd2; clone AF4) were purchased from KOMP repository. Shown is Smarcd2tm1(KOMP)Vlcg (deletion allele). The positions of the primer pairs for the wild-type allele (empty arrowheads) and the knockout allele (filled arrowheads) are shown in relation to the Smarcd2 gene and deletion allele, respectively. (b) PCR-based genotyping. F1 intercrosses of heterozygous mice resulted in Smarcd2+/+, Smarcd2+/−, and Smarcd2−/− embryos. PCR was performed according to the manufacturer (KOMP repository): wild-type allele, 264 bp (empty arrowheads) and knockout allele, 569 bp (filled arrowheads). Embryos 13, 15, and 17 are of the knockout genotype (Smarcd2−/−), and embryos 12, 14, and 16 are of the heterozygous genotype (Smarcd2+/−). Images have been cropped; full-length images are shown in Supplementary Data 3d,e. (c–e) Mendelian inheritance pattern of mutant Smarcd2 alleles. (c) Knockout embryos are not viable after birth. The numbers of Smarcd2+/+ (n = 24), Smarcd2+/− (n = 52), and Smarcd2−/− (n = 1, perinatal death) offspring born are displayed. (d) The distributions of genotypes per litter (in percent) are displayed. In total, expected Mendelian ratios of the genotypes (percent of genotype per litter) are observed in utero. Data from 15 litters are shown; compare with Supplementary Table 20. Center value, mean; error bars, s.e.m. P values were calculated by two-tailed unpaired t test. (e) The number of embryos per genotype and gestational age are shown at 12.5, 13.5, 14.5, 15.5, and 16.5 d.p.c. In total, wild type n = 24, heterozygous n = 56, and knockout n = 27 embryos were observed. (f) Western blot analysis detecting members of the SWI/SNF complex in Smarcd2-knockout embryos. Protein expression of SMARCD1 (BAF60a), SMARCD2 (BAF60b), SMARCD2 (BAF60c) (kindly provided by J. Lessard, Montreal), and SWI/SNF members BRG1, BAF170, BAF155, and BAF47 are shown. Images of membranes have been cropped; full images are available in Supplementary Data 4. Protein expression was determined in crude embryonic tissue lysates by western blotting. Embryos from two litters were analyzed: wild type n = 3, heterozygous n = 3, knockout n = 3. Replicates: 1. (g) Enumeration of total white blood cells (CD45.2+) and the stem cell compartment (LSK cells and LSK CD150+CD48− cells) per embryo in wild-type, heterozygous, and knockout mouse fetal liver hematopoiesis. Smarcd2−/− embryos show reduced CD45.2+ blood cells but comparable amounts of stem cells (LSK, LSK CD150+CD48−). Data are from three litters: wild type n = 7; heterozygous n = 10; knockout n = 8. Center value, mean; error bars, s.e.m. P values were calculated by two-tailed unpaired t test. Replicates: 1.
(a) Comprehensive analysis of myeloid cell colonies. Data are from five experiments with eight litters: wild type n = 10, heterozygous n = 13, knockout n = 12. Numbers of colonies have been normalized to the input of 500 LSK cells. Center value, mean; error bars, s.e.m. P values were calculated by two-tailed unpaired t test. The F test when performed to compare the variances of the wild-type, heterozygous, and knockout groups showed, that variances differed significantly in total colonies (wild type vs. heterozygous, ***P < 0.001; wild type vs. knockout, ***P < 0.001), GM colonies (wild type vs. heterozygous, ***P < 0.001; wild type vs. knockout, **P = 0.003), M colonies (wild type vs. knockout, *P = 0.011), and G colonies (wild type vs. heterozygous, *P = 0.036; wild type vs. knockout, ***P < 0.001). Unpaired t tests with Welch’s correction showed that differences in means are significant in total colonies (wild type vs. heterozygous, *P = 0.037; wild type vs. knockout, **P = 0.004), in GM colonies (wild type vs. heterozygous, *P = 0.019; wild type vs. knockout, *P = 0.013), in M colonies (wild type vs. knockout, *P = 0.022), and in G colonies (wild type vs. knockout, *P = 0.011). This is likely to be due to sampling of experiments, outliers, and low numbers of colonies in M/G knockout samples. (b) Representative FACS plots of myeloid GM colonies derived from a showing expression of myeloid surface markers. Numbers are representative of the percentage of CD11b+Gr1+ and CD11b+Ly6c+ cells. CD11b+Gr1+ and CD11b+Ly6c+ cells are absent in Smarcd2−/− colonies. Data shown are from one experiment (wild type n = 1, heterozygous n = 2, knockout n = 2), subsequently confirmed by a second experiment with wild type n = 5, heterozygous n = 4, and knockout n = 6, for which data are not shown. Replicates: 2.
Supplementary Figure 9 Differentially expressed genes in mouse Smarcd2-deficient early progenitors affect myeloid pathways.
(a) Differentially expressed genes in Smarcd2+/+ versus Smarcd2−/− mouse LSK cells cluster in 11 groups by Reactome FI spectral clustering. Pathways cluster significantly in immune system and myeloid pathways. Smarcd2 is highlighted in red. Relevant pathways and interactions between pathways are indicated. The sources of pathway annotations are indicated in parentheses: C, CellMap; R, Reactome; K, KEGG; N, NCI PID; P, Panther; B, BioCarta. A complete list of pathways enriched per cluster is shown in Supplementary Table 6a. (b) Venn diagram of differentially expressed genes in Smarcd2+/+ versus Smarcd2−/− LSK cells and CEBPɛ target genes (Supplementary Table 6c). (c) Differentially expressed genes in Smarcd2+/+ versus Smarcd2−/− mouse LSK cells overlap with CEBPɛ targets (13 genes) and interact via MYC, FOS, EP300, and the ubiquitin system. Genes in green diamonds have been introduced as linker genes; differentially expressed genes are color-coded by continuous mapping of log(fold change) generated in LSK Smarcd2+/+ versus Smarcd2−/− RNA–seq experiments (blue, reduced expression in knockout; red, increased expression in knockout). Analysis and display of the network were carried out using Cytoscape 3.3.0 and the Reactome Functional Interaction (FI) plugin (solid line with arrow for activating/catalyzing FI, solid line with block for inhibitory FI, solid line (alone) for FIs extracted from complexes or inputs, and dotted lines for predicted FIs). The genes for all intersections are listed in Supplementary Table 6c.
(a–c) Representative example of wild-type (a) and knockout (b) fetal liver hematopoiesis (per embryo) and gating strategy (c). Cells were first discriminated by FSC/SSC (data not shown) and then by SSC-H/CD45. CD45+ cells were gated on Lin−c-Kit+ cells. CD45+Lin− Sca-1+c-Kit+ (LSK) cells were sorted, and CD45+Lin−CD117+Sca-1− (myeloid progenitor) cells were further separated into CD45+Lin−Sca-1−c-Kit+CD34−CD16/32lo MEPs, CD45+Lin−Sca-1−c-Kit+CD34+CD16/32int CMPs, and CD45+Lin−Sca-1−c-Kit+CD34+CD16/32hi GMPs. In comparison to a, GMP cells are almost absent in b. (c) Numbers in black boxes refer to the percentage of wild-type cells, and numbers in white boxes refer to the percentage of knockout cells.
Supplementary Figure 11 Promoter occupancy of target genes for the CEBPɛ and BRG1 proteins in SMARCD2-deficient NB4 cells.
(a–c) CEBPɛ and BRG1 bind to the promoter regions of MMP8 (a), CAMP (b), and SERPIN A1 (c). Although binding is not significantly reduced in cells transduced with shRNA1 (P = ns) or shRNA2 (P = ns) in comparison to cells transduced with a nonspecific control shRNA (CTRL), a trend can be observed. The experiment was performed two times. Data points from two experiments with a total of five biological replicates (five independent cultures and ChIP immunoprecipitations) are merged. Center value, mean; error bars, s.d. P values were calculated by two-tailed unpaired t test. Replicates: 3.
(a–d) Experiment 1. (a) Immunoblotting for SMARCD2 detects SMARCD2 in a CEBPɛ immunoprecipitate in short and long exposures; a distinct band is noted (red arrow) at the expected size of ~56 kDa, corresponding to input and coimmunoprecipitated SMARCD2 proteins. (b) Cropped lanes of a showing immunoprecipitation with isotype control and antibody to CEBPɛ (a2). (c) CEBPɛ is detected in input and immunoprecipitate; the image was cropped (c3) for summary. (d) Cropped images highlighting bands from experiment 1 shown with standard kDa marker (PageRuler Prestained Protein Ladder, Thermo Fisher). (e–g) Experiment 2. (e) Immunoblotting for SMARCD2 detects SMARCD2 in two independent CEBPɛ immunoprecipitates from the same lysate (technical replicates). Distinct bands are noted (red arrows) at the expected size of ~56 kDa, corresponding to input and coimmunoprecipitated SMARCD2 proteins (e1). Immunoblotting for GAPDH shows the presence of GAPDH in input but not in immunoprecipitates (e3). (f) CEBPɛ is detected in input and immunoprecipitates (red arrows) (f2). (g) Cropped images highlighting bands from experiment 2 shown with standard kDa marker (PageRuler Prestained Protein Ladder, Thermo Fisher). (h–j) Experiment 3. (h) Immunoblotting for SMARCD2 detects SMARCD2 in the CEBPɛ immunoprecipitate. A distinct band is noted (red arrow) at the expected size of ~56 kDa, corresponding to input and coimmunoprecipitated SMARCD2 (h1). Immunoblotting for GAPDH shows the presence of GAPDH in Input but not in immunoprecipitates (red arrow) (h3). (i) CEBPɛ is detected in input and immunoprecipitates (red arrows) (i2). (j) Cropped images highlighting bands from experiment 3 shown with standard kDa marker (Precision Plus Protein Kaleidoscope Prestained Protein Standards, Bio-Rad). The protein standard ladders differ between experiment 1 and 2 and experiment 3.
(a) Differentially expressed genes in undifferentiated AML-NB4 cells (shRNA-mediated SMARCD2 knockdown versus control) cluster in 11 groups by Reactome FI spectral partition and show significant enrichment for myeloid pathways. SMARCD2 is highlighted in red. Relevant pathways and interactions between pathways are indicated. The sources of pathway annotations are indicated in parentheses: C, CellMap; R, Reactome; K, KEGG; N, NCI PID; P, Panther; B, BioCarta. A complete list of the pathways enriched per cluster is given in Supplementary Table 6e. (b) Differentially expressed genes in ATRA-differentiated AML-NB4 cells (shRNA-mediated SMARCD2 knockdown versus control) cluster in 12 groups by Reactome FI spectral partition and show significant enrichment for myeloid pathways. SMARCD2 is highlighted in red. Relevant pathways and interactions between pathways are indicated. The sources of pathway annotations are indicated in parentheses: C, CellMap; R, Reactome; K, KEGG; N, NCI PID; P, Panther; B, BioCarta. A complete list of the pathways enriched per cluster is shown in Supplementary Table 6f. (c) Venn diagram of differentially expressed genes (undifferentiated and ATRA differentiated) and CEBPɛ target genes. Genes from all intersections are listed in Supplementary Table 6d. (d) Differentially expressed genes in ATRA-differentiated AML-NB4 cells overlap with CEBPɛ targets (21 genes) and interact via EP300, TP53, STAT1, and the ubiquitin system. Genes in green diamonds have been introduced as linker genes; differentially expressed genes are color-coded by continuous mapping of log(fold change) in SMARCD2-knockdown cells versus control cells (blue, reduced expression in SMARCD2-knockdown cells; red, increased expression in SMARCD2-knockdown cells). Analysis and display of the network were carried out with Cytoscape 3.3.0 and the Reactome Functional Interaction (FI) plugin: solid lines with arrows for activating/catalyzing FIs, solid lines with blocks for inhibitory FIs, solid lines (alone) for FIs extracted from complexes or inputs, and dotted lines for predicted FIs. This data set is derived from NB4 cells exposed to 1 μM ATRA for 2 d and, thus, cannot directly be compared to the qPCR data shown in Figure 5a.
Supplementary Figure 14 Regions of altered chromatin accessibility cluster around transcription start sites.
(a) Regions of open chromatin cluster around transcription start sites (TSSs) in DMSO/mock-treated NB4 cells. Peaks were binned into 500-bp windows with respect to their distance to the TSS. Each bar represents the fraction of peaks falling into one bin against all peaks of one group. The peaks are grouped as all peaks (black), upregulated peaks (red), and downregulated peaks (blue). The depicted peak distribution is based on undifferentiated (DMSO vehicle control) NB4 cells. (b) As in a but based on ATRA-differentiated NB4 cells.
Supplementary Figures 1–14, Supplementary Note and Supplementary Tables 1, 2 and 18 (PDF 3733 kb)
Supplementary Data 1–5 (PDF 13450 kb)
Primers for human, mouse, and zebrafish studies; morpholinos and sgRNAs for zebrafish studies. (XLSX 16 kb)
Differentially expressed genes in Smarcd2+/+ vs. Smarcd2−/− LSK cells. (XLSX 517 kb)
Up- and downregulated clusters of genes in Smarcd2+/+ vs. Smarcd2−/− LSK cells. (XLSX 34 kb)
CEBPɛ target genes, Venn intersections, and pathways. (XLSX 53 kb)
Differentially expressed genes in Smarcd2+/+ vs. Smarcd2−/− LSK cells. (XLSX 15 kb)
Differentially expressed genes in Smarcd2+/+ vs. Smarcd2−/− CMP cells. (XLSX 159 kb)
Differentially expressed genes in Smarcd2+/+ vs. Smarcd2−/− GMP cells. (XLSX 77 kb)
Differentially expressed genes in Smarcd2+/+ vs. Smarcd2−/− MEP cells. (XLSX 38 kb)
Up- and downregulated GO terms in Smarcd2+/+ vs. Smarcd2−/− CMP cells. (XLSX 21 kb)
Up- and downregulated GO terms in Smarcd2+/+ vs. Smarcd2−/− GMP cells (XLSX 19 kb)
Up- and downregulated GO terms in Smarcd2+/+ vs. Smarcd2−/− LSK cells. (XLSX 10 kb)
Up- and downregulated GO terms in Smarcd2+/+ vs. Smarcd2−/− MEP cells. (XLSX 20 kb)
Differentially expressed genes in ATAC–seq and RNA–seq, CTRL vs. shRNA1-, shRNA2-treated NB4 cells, vehicle DMSO treated. (XLSX 7374 kb)
Differentially expressed genes in ATAC–seq and RNA–seq, CTRL vs. shRNA1-, shRNA2-treated NB4 cells, ATRA treated. (XLSX 2427 kb)
Available blood counts of patients A, B, and C, chronologically arranged. (XLSX 31 kb)
Definition and number of replicates performed per experiment. (XLSX 31 kb)
Numbers used for dot-bot diagrams and statistical analysis, statistical test results. (XLSX 464 kb)
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Witzel, M., Petersheim, D., Fan, Y. et al. Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes. Nat Genet 49, 742–752 (2017). https://doi.org/10.1038/ng.3833
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