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Regulation of nucleosome landscape and transcription factor targeting at tissue-specific enhancers by BRG1
Open accessAbstract
Enhancers of transcription activate transcription via binding of sequence-specific transcription factors to their target sites in chromatin. In this report, we identify GATA1-bound distal sites genome-wide and find a global reorganization of the nucleosomes at these potential enhancers during differentiation of hematopoietic stem cells (HSCs) to erythrocytes. We show that the catalytic subunit BRG1 of BAF complexes localizes to these distal sites during differentiation and generates a longer nucleosome linker region surrounding the GATA1 sites by shifting the flanking nucleosomes away. Intriguingly, we find that the nucleosome shifting specifically facilitates binding of TAL1 but not GATA1 and is linked to subsequent transcriptional regulation of target genes.
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“The mechanisms of pioneer factor action are still being established [37], but at least some of them (such as FOXA, OCT4 and SOX2/SOX11) have been shown to initiate chromatin opening by direct displacement of histones [38–41], whilst many others recruit chromatin remodelers [42–50].”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [48]
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Cites
Mapping and quantifying mammalian transcriptomes by RNA-Seq
Mortazavi, A., Williams, B. A., McCue, K., Schaeffer, L., & Wold, B. (2008) · Nature Methods · doi:10.1038/nmeth.1226 · Cited by 13,696
High-Resolution Profiling of Histone Methylations in the Human Genome
Barski, A., Cuddapah, S., Cui, K., Roh, T.-Y., Schones, D. E., Wang, Z., Wei, G., Chepelev, I., & Zhao, K. (2007) · Cell · doi:10.1016/j.cell.2007.05.009 · Cited by 6,845
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Research works printed but not linked: 51
- 10.1016/S0092-8674(00)81785-7 · DOI
- 10.1093/nar/gkl198 · DOI
- 10.1006/jmbi.1998.1783 · DOI
- 10.1016/S1097-2765(00)00127-1 · DOI
- 10.1038/nsmb1333 · DOI
- 10.1038/sj.onc.1205326 · DOI
- 10.1101/gr.098921.109 · DOI · Paper page
- 10.1093/nar/gkp507 · DOI
- 10.1038/nature00876 · DOI
- 10.1128/MCB.24.10.4476-4486.2004 · DOI
- 10.1016/j.stem.2008.11.011 · DOI
- 10.1016/j.molcel.2005.02.024 · DOI
- 10.1016/j.molcel.2009.11.001 · DOI
- 10.1074/jbc.M609847200 · DOI
- 10.1038/ng.545 · DOI
- 10.1073/pnas.0812888106 · DOI
- 10.1073/pnas.0506164102 · DOI
- 10.1038/370481a0 · DOI
- 10.1084/jem.20080938 · DOI
- 10.1016/j.molcel.2008.02.010 · DOI
- 10.1016/S1097-2765(03)00034-0 · DOI
- 10.1038/nature07667 · DOI
- 10.1101/gr.104935.110 · DOI
- 10.1093/nar/gkp677 · DOI
- 10.1073/pnas.0806420106 · DOI
- 10.1073/pnas.0811274106 · DOI
- 10.1016/S0092-8674(01)00446-9 · DOI
- 10.1128/MCB.22.18.6471-6479.2002 · DOI
- 10.4049/jimmunol.178.1.345 · DOI
- 10.1038/ni.1619 · DOI
- 10.1073/pnas.96.2.349 · DOI
- 10.1073/pnas.92.21.9585 · DOI · Paper page
- 10.1016/S0092-8674(00)80076-8 · DOI
- 10.1016/j.cell.2009.04.020 · DOI
- 10.1093/bioinformatics/btp616 · DOI · Paper page
- 10.1016/j.cell.2008.02.022 · DOI
- 10.1371/journal.pone.0009129 · DOI
- 2010, Widespread remodeling of mid-coding sequence nucleosomes by Isw1, Genome Biol, 11, R49, 10.1186/gb-2010-11-5-r49 · DOI
- 10.1182/blood-2008-07-169417 · DOI
- 10.1093/emboj/16.11.3145 · DOI
- 1996, Purification and biochemical heterogeneity of the mammalian SWI-SNF complex, EMBO J, 15, 5370, 10.1002/j.1460-2075.1996.tb00921.x · DOI
- 10.1038/nature06391 · DOI
- 10.1182/blood-2009-01-200048 · DOI
- 10.1016/j.stem.2010.07.016 · DOI · Paper page
- 10.1016/j.neuron.2007.08.021 · DOI
- 10.1128/MCB.00835-08 · DOI
- 10.1016/j.molcel.2009.11.002 · DOI
- 10.1093/bioinformatics/btp340 · DOI
- 10.1186/gb-2008-9-9-r137 · DOI · Paper page
- 10.1186/1471-2164-9-537 · DOI
- 10.1016/S0092-8674(00)81633-5 · DOI
Cited by
Sorted by citations
Items 101–174 of 174
Wei, G., Hu, G.-Q., Cui, K.-R., & Zhao, K.-J. (2012) · Methods in Enzymology · doi:10.1016/b978-0-12-391938-0.00013-6 · Cited by 28
“Another aspect of transcriptional regulation through chromatin structure is mediated by reorganization of nucleosome occupancy and positioning, which impact the accessibility of genomic target sites for transcription factors and transcription machinery to regulate gene expression (Henikoff, Furuyama, & Ahmad, 2004; Hu…”
BackgroundSelf-citationChromatin regulation and dynamics in stem cells
Klein, D. C., & Hainer, S. J. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.11.002 · Cited by 41
“Along with OCT4 and SOX2, additional pioneer factors, such as p63, GATA, and AP-1 have been reported to recruit nucleosome remodeling factors to their target sites (Bao et al., 2015; Engelen et al., 2011; Hu et al., 2011; Takaku et al., 2016; Vierbuchen et al., 2017).”
BackgroundWenderski, W., & Maze, I. S. (2016) · BioEssays · doi:10.1002/bies.201500171 · Cited by 31
“The BAF complex additionally influences transcriptional initiation by increasing nucleosomal spacing at enhancer elements, a phenomenon that has recently been demonstrated during the process of hematopoiesis [66].”
BackgroundGenetic Modifiers of the Breast Tumor Microenvironment
Flister, M. J., & Bergom, C. R. (2018) · Trends in cancer · doi:10.1016/j.trecan.2018.04.003 · Cited by 24
Chatterjee, S., Biswas, M., Boila, L. D., Banerjee, D., & Sengupta, A. (2018) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-17-0493 · Cited by 24
“SWI/SNF was shown to play chromatin remodeling function at both promoters and enhancers (30, 48).”
BackgroundTaking into account nucleosomes for predicting gene expression
Teif, V. B., Erdel, F., Beshnova, D. A., Vainshtein, Y., Mallm, J., & Rippe, K. (2013) · Methods · doi:10.1016/j.ymeth.2013.03.011 · Cited by 22
Pioneer Factors in Animals and Plants—Colonizing Chromatin for Gene Regulation
Lai, X., Verhage, L., Hugouvieux, V., & Zubieta, C. (2018) · Molecules · doi:10.3390/molecules23081914 · Cited by 31
Using epigenetic mechanisms to understand the impact of common disease causing alleles
Leung, A., Schones, D. E., & Natarajan, R. D. (2012) · Current Opinion in Immunology · doi:10.1016/j.coi.2012.07.004 · Cited by 21
Self-citationRichards, L. A., Kumari, A., Knezevic, K., Thoms, J. A. I., von Jonquières, G., Napier, C. E., Ali, Z., O’Brien, R., Marks-Bluth, J., Maritz, M. F., et al. (2019) · Haematologica · doi:10.3324/haematol.2018.215699 · Cited by 25
Romano, O., Peano, C., Tagliazucchi, G. M., Petiti, L., Poletti, V., Cocchiarella, F., Rizzi, E., Severgnini, M., Cavazza, A., Rossi, C., et al. (2016) · Scientific Reports · doi:10.1038/srep24724 · Cited by 22
BRG1 knockdown inhibits proliferation through multiple cellular pathways in prostate cancer
Giles, K., Gould, C. M., Achinger-Kawecka, J., Page, S. G., Kafer, G., Rogers, S., Luu, P.-L., Cesare, A. J., Clark, S., & Taberlay, P. (2021) · Clinical Epigenetics · doi:10.1186/s13148-021-01023-7 · Cited by 21
Takesue, H., Hirota, T., Tachimura, M., Tokashiki, A., & Ieiri, I. (2018) · Molecular Pharmacology · doi:10.1124/mol.118.111807 · Cited by 21
“Previous studies demonstrated that nucleosomes control tissue-specific transcription factor binding to gene promoters, and, thus, contribute to tissue-specific gene expression (Hoffman et al., 2010; Hu et al., 2011; Tsui et al., 2011; Yang et al., 2013; Zhang et al., 2015).”
BackgroundRogers, H. M., Wang, L., Yu, X., Alnaeeli, M., Cui, K., Zhao, K., Bieker, J. J., Prchal, J. T., Huang, S., Weksler, B. B., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.378398 · Cited by 18
“Importantly, shifting the nucleosomepositioning can specifically facilitate binding of TAL1 and is linked to subsequent transcriptional regulation of target genes (44), providing further support for the suggestion that the expanded linker region of EPO-R in CD36 cells facilitates TAL1 binding to the EPO-R promoter and…”
BackgroundSelf-citationChromatin Alterations in Neurological Disorders and Strategies of (Epi)Genome Rescue
Janowski, M., Milewska, M., Zare, P., & Pękowska, A. (2021) · Pharmaceuticals · doi:10.3390/ph14080765 · Cited by 21
McAndrew, M. J., Gjidoda, A., Tagore, M. M., Miksanek, T., & Floer, M. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.734186 · Cited by 18
Deciphering cis -regulatory control in inflammatory cells
Ghisletti, S., & Natoli, G. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0370 · Cited by 19
“GATA1-mediated recruitment of BRG1 and subsequent nucleosome shifting facilitate binding of TAL1, a key TF for haematopoiesis [2].”
BackgroundProfiling of pluripotency factors in individual stem cells and early embryosPreprint
Hainer, S. J., Bošković, A., Rando, O. J., & Fazzio, T. G. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/286351 · Cited by 15
“…component of the esBAF nucleosome remodeling complex that activates enhancers by creating open chromatin structure—is required for association of OCT4 with approximately 60% of its normal genomic binding sites (Hainer and Fazzio, 2015; Hodges et al., 2018; Hu et al., 2011; King and Klose, 2017).”
BackgroundLi, J., Xu, J., Jiang, H., Zhang, T., Ramakrishnan, A., Shen, L., & Xu, P. (2021) · Journal of the American Society of Nephrology · doi:10.1681/asn.2021040525 · Cited by 21
Kumar, M., Majumder, D., Mal, S., Chakraborty, S., Gupta, P., Jana, K., Gupta, U. D., Ghosh, Z., Kundu, M., & Basu, J. (2019) · Cellular Microbiology · doi:10.1111/cmi.13142 · Cited by 19
“BRG1 is required for differentiation of lymphoid and myeloid cells (Choi et al., 2012; Hu et al., 2011; Kowenz‐Leutz & Leutz, 1999).”
BackgroundCTCF and cellular heterogeneity
Ren, G., & Zhao, K. (2019) · Cell & Bioscience · doi:10.1186/s13578-019-0347-2 · Cited by 20
Self-citationKyrochristos, I. D., Glantzounis, G. K., Ziogas, D. E., Gizas, I., Schizas, D., Lykoudis, E. G., Felekouras, E. S., Machairas, A., Katsios, C. G., Liakakos, T., et al. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18010180 · Cited by 18
Genome-wide analysis reveals positional-nucleosome-oriented binding pattern of pioneer factor FOXA1
Ye, Z., Chen, Z., Sunkel, B. D., Frietze, S. E., Huang, T. H. ‐., Wang, Q., & Jin, V. X. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw659 · Cited by 19
Yun, H., Narayan, N., Vohra, S., Giotopoulos, G., Mupo, A., Madrigal, P., Sasca, D., Lara‐Astiaso, D., Horton, S. J., Singh, S. A., et al. (2021) · Nature Genetics · doi:10.1038/s41588-021-00925-9 · Cited by 38
“Using published data (including ChIP-seq on H3K4me1 6 and CTCF 37 , ATAC-seq 38 , together with pCHiC 18 ) of human CD34+ HSPC, we could demonstrate that the interaction was also present across species, and ChIP-seq data from ourselves 39 and others 40,41 indicated that this region also contained a SE in human AML cel…”
Cornes, B. K., Brody, J. A., Nikpoor, N., Morrison, A. C., Dang, H. C. P., Ahn, B. S., Wang, S., Dauriz, M., Barzilay, J. I., Dupuis, J., et al. (2014) · Circulation Cardiovascular Genetics · doi:10.1161/circgenetics.113.000169 · Cited by 14
EBF1 is continuously required for stabilizing local chromatin accessibility in pro-B cells
Zolotarev, N., Bayer, M., & Grosschedl, R. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2210595119 · Cited by 13
“The initial binding of pioneer TFs is unstable but it can be stabilized by the recruitment of chromatin remodeling complexes (36, 37) (reviewed in ref.”
BackgroundCerván-Martín, M., Bossini-Castillo, L., Rivera‐Egea, R., Garrido, N., Luján, S., Romeu, G., Santos-Ribeiro, S., Castilla, J., Gonzalvo, M. D. C., Clavero, A., et al. (2021) · Andrology · doi:10.1111/andr.13009 · Cited by 13
“Regarding CDC42BPA- rs3000811 (associated with NOA in the GWASs by Hu et al11,12 and with MA in our study), the complete LD block spanned a total of 92 SNPs and up to 54.5 kb in chromosome 1 (Figure 2).”
BackgroundMethodInfluentialShidlovskii, Y. V., Bylino, O. V., Shaposhnikov, A. V., Kachaev, Z. M., Lebedeva, L. A., Kolesnik, V. V., Amendola, D., Simone, G. D., Formicola, N., Schedl, P. D., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22062856 · Cited by 13
“SWI/SNF similarly establishes the nucleosome landscape on enhancers [48,53], and its participation in local histone acetylation has also been described [46].”
BackgroundUechi, L., Dashti, M. J. S., Wilbur, J. D., French, J. L., Jumbe, N. L., Meaney, M. J., Gluckman, P. D., Karnani, N., Sakhanenko, N. A., Galas, D. J., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0242684 · Cited by 12
Insights Into the Emerging Role of Baf53b in Autism Spectrum Disorder
Rowland, M. E., Jajarmi, J. M., Osborne, T. S. M., & Ciernia, A. V. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.805158 · Cited by 16
“These data suggest that the BAF complex is required for establishment and maintenance of accessible chromatin that allows for celltype specific transcription factor binding (Iurlaro et al., 2021; Schick et al., 2021).”
BackgroundYadav, V., Thakur, R. K., Eckloff, B., Baral, A., Singh, A., Halder, R., Kumar, A., Alam, M. P., Kundu, T., Pandita, R., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku596 · Cited by 12
“Other studies found that nucleosome repositioning events may facilitate TF binding and gene expression upon androgen treatment (19), during differentiation of hematopoietic stem cells to erythrocytes (20), or interferon-beta activation following virus infection (21).”
BackgroundEpigenetic and genetic mechanisms in red cell biology
Hewitt, K. J., Sanalkumar, R., Johnson, K. D., Keleş, S., & Bresnick, E. H. (2014) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000034 · Cited by 12
“The Brahmarelated gene 1 (BRG1) component of the switch/ sucrose non-fermentable (SWI/SNF) chromatin remodeling complex induces chromatin accessibility at GATA-1-occupied enhancers [64,65].”
BackgroundLazar, J. E., Stehling-Sun, S., Nandakumar, V., Wang, H., Chee, D. R., Howard, N. P., Acosta, R., Dunn, D., Diegel, M., Neri, F. J., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107676 · Cited by 14
A SWI/SNF-specific Ig-like domain, SWIFT, is a transcription factor binding platform
Jain, S. U., Williamson, K. E., Ying, A. W., Turner, A. M., Jiang, R. J., Raval, S., So, K., Allison, M. J., Sankar, A., Sáme Guerra, D. D., et al. (2026) · Science · doi:10.1126/science.aeb3627 · Cited by 11
DNA G-quadruplex structures act as functional elements in α- and β-globin enhancers
Doyle, C., Herka, K., Flynn, S. M., Melidis, L., Dhir, S., Schoenfelder, S., Tannahill, D., & Balasubramanian, S. (2025) · Genome biology · doi:10.1186/s13059-025-03627-1 · Cited by 10
“We next determined whether a folded G4 structure influences chromatin accessibility in the HS-40 and HS2 globin enhancers, as nucleosome organization is critical for enhancer activity [57–59] and it is known that G4s are involved in determining an open chromatin state in promoters [5, 60].”
Baf155 controls hematopoietic differentiation and regeneration through chromatin priming
Wu, J., Fan, C., Kabir, A. U., Krchma, K., Kim, M., Kwon, Y., Xing, X., Wang, T., & Choi, K. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114558 · Cited by 7
nucMACC: An MNase-seq pipeline to identify structurally altered nucleosomes in the genome
Wernig-Zorc, S., Kugler, F., Schmutterer, L., Räß, P., Hausmann, C., Holzinger, S., Längst, G., & Schwartz, U. (2024) · Science Advances · doi:10.1126/sciadv.adm9740 · Cited by 16
“Regulatory regions, such as promoters, enhancers, and insulators, are characterized by well-positioned nucleosomes, which is a common feature of eukaryotic chromatin ( 12 , 13 ).”
BackgroundCorrelating Histone Modification Patterns with Gene Expression Data During Hematopoiesis
Hu, G.-Q., & Zhao, K.-J. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-0512-6_11 · Cited by 9
“Download the RNA-Seq BED file from GEO (GSM651554) [14].”
MethodSelf-citationShin, C. Y., Gokbayrak, B., Tao, V. L., Almadani, N., Li, E., Ho, R., Kommoss, F. K. F., Huvila, J. K., Chiu, D. S., Leung, S. C. Y., et al. (2025) · Histopathology · doi:10.1111/his.15411 · Cited by 9
Inherited variants in genes somatically mutated in thyroid cancer
Campo, C., Köhler, A., Figlioli, G., Elisei, R., Romei, C., Cipollini, M., Bambi, F., Hemminki, K., Gemignani, F., Landi, S., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174995 · Cited by 8
An approach of identifying differential nucleosome regions in multiple samples
Liu, L., Xie, J., Sun, X., Luo, K., Qin, Z., & Liu, H.-D. (2017) · BMC Genomics · doi:10.1186/s12864-017-3541-9 · Cited by 8
Dynamic nucleosome landscape elicits a noncanonical GATA2 pioneer model
Li, T., Liu, Q., Chen, Z., Fang, K., Huang, F., Fu, X., Wang, Q., & Jin, V. X. (2022) · Nature Communications · doi:10.1038/s41467-022-30960-x · Cited by 6
HELLS is required for maintaining proper DNA modification at human satellite repeats
Guckelberger, P., Haut, L., Tornisiello, R., Kretzmer, H., & Meissner, A. (2025) · Genome Biology · doi:10.1186/s13059-025-03681-9 · Cited by 6
From Genotype to Phenotype: How Enhancers Control Gene Expression and Cell Identity in Hematopoiesis
Mulet‐Lazaro, R., & Delwel, R. (2023) · HemaSphere · doi:10.1097/hs9.0000000000000969 · Cited by 11
“…and colleagues first coined the term “pioneer factors” to describe FOXA (HNF3) and GATA4, after demonstrating they bind nucleosome arrays and open compacted chromatin, 77 but multiple other LDTFs have a similar function in the hematopoietic system, including C/EBP β , 78 GATA1, 79,80 and PU.1.”
BackgroundPeinado, P., Andrades, Á., Martorell-Marugán, J., Haswell, J. R., Slack, F., Carmona-Sáez, P., & Medina, P. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab187 · Cited by 6
nucMACC: A MNase-seq pipeline to identify structurally altered nucleosomes in the genome
Sara, W.-Z., Fabian, K., Leo, S., Patrick, R., Clemens, H., Simon, H., Gernot, L., & Uwe, S. (2023) · bioRxiv · doi:10.1101/2022.12.29.521985 · Cited by 5
“Regulatory regions, such as promoters, enhancers, and insulators, are characterized by well-57 positioned nucleosomes, which is a common feature of eukaryotic chromatin (Hu et al , 2011; Schones et al , 2008).”
BackgroundThe Role of Nucleosomes in Epigenetic Gene Regulation
Giles, K. A., & Taberlay, P. C. (2019) · Springer eBooks · doi:10.1007/978-981-13-8958-0_4 · Cited by 10
SWI/SNF deficient tumors - morphology, immunophenotype, genetics, epigenetics, nosology and therapy.
Ng, C., & Qin, J.-L. (2024) · Laboratory investigation; a journal of technical methods and pathology · doi:10.1016/j.labinv.2024.102185 · Cited by 4
Chromatin—a global buffer for eukaryotic gene control
Moshkin, Y. M. (2015) · AIMS Biophysics · doi:10.3934/biophy.2015.4.531 · Cited by 4
“Nucleosome phasing is found in the vicinity to Ori Recognition Complex sites (ORC), CCCTC-binding factor (CTCF) sites and so on [144–147].”
Ovarian small cell carcinoma in one of a pair of monozygous twins
Fahiminiya, S., Sabbaghian, N., Albrecht, S., Nadaf, J., Callegaro‐Filho, D., & Foulkes, W. (2018) · Familial Cancer · doi:10.1007/s10689-018-0108-0 · Cited by 3
A Hierarchical Framework for State-Space Matrix Inference and Clustering
Zuo, C., Chen, K.-L., Hewitt, K., Bresnick, E., & Keleş, S. (2015) · Annals of Applied Statistics · doi:10.1214/16-aoas938 · Cited by 3
“, 2009a,b) and co-localizes with GATA1 at some chromatin sites (Hu et al., 2011).”
BackgroundWhat Can We Learn from Flies: Epigenetic Mechanisms Regulating Blood Cell Development in Drosophila
Badenhorst, P. (2014) · Epigenetics and human health · doi:10.1007/978-3-642-45198-0_2 · Cited by 3
“There is also evidence from mammalian systems implicating the SWI/SNF subtype complexes BAF and PBAF in haematopoiesis (Bultman et al. 2005) and that these SWI/SNF complexes may be involved in facilitating binding of TAL1 to chromatin (Bultman et al. 2005; Hu et al. 2011).”
BackgroundGong, H., Hu, B., Nie, L., Zhang, H.-F., Wang, P., Xu, W., Li, M., Liu, L., Zhang, J., Xiao, X.-J., et al. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkaf1506 · Cited by 2
“Previous studies have demonstrated that GA T A1 and TAL1 interact with BRG1 to regulate erythroid gene expression [ 45 –47 ].”
Matur, M., Uzun, Y., Shi, X. E., Hamamoto, K., Qiu, Y., & Huang, S. (2025) · Molecular and Cellular Biology · doi:10.1080/10985549.2025.2482079 · Cited by 4
Self-citationLiu, Y., Yin, A., Seese, K., Fu, W., & Yin, H. (2025) · Obesity · doi:10.1002/oby.24280 · Cited by 2
“The afore-mentioned putative functions of ncBAF/Brd9 echoes its reported roles in lineage specification [38, 42, 43].”
PC Gene Affects Milk Production Traits in Dairy Cattle
Du, A.-X., Guo, Z., Chen, A., Xu, L., Sun, D.-X., & Han, B. (2024) · Genes · doi:10.3390/genes15060708 · Cited by 2
Yun, H.-Y., Vohra, S., Mupo, A., Giotopoulos, G., Sasca, D., Horton, S., Agrawal-Singh, S., Meduri, E., Basheer, F., Marando, L., et al. (2019) · bioRxiv · doi:10.1101/2020.03.20.000059 · Cited by 2
Kaur, H., Sood, V., Choubey, P., Sawant, M., Gogate, A., Gupta, A., & Bansal, K. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117604 · Cited by 1
Jin, Y., Hasegawa, Y., Zhou, Z., Lin, J. T., Leung, A. K.-Y., Yu, H., & Lis, J. T. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.16.706221
“Together, these observations support a model in which GATA1-dependent activity at enhancer_86 promotes SWI/SNF dependent chromatin opening at both the enhancer and its target promoter, thereby enabling transcriptional activation of an otherwise inaccessible promoter 52 .”
Saha, D., Animireddy, S., Lee, J., Lin, Y.-C., Feola, K. C., Jain, A. K., Lu, Y., Liu, B., & Bartholomew, B. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.06.506785 · Cited by 1
“increasing accessibility at the enhancers (Bossen et al., 2015; Hu et al., 2011; Ni et al., 2008).”
BackgroundInfluentialMeng, N., Machiraju, R., & Huang, K. (2016) · BMC Bioinformatics · doi:10.1186/s12859-016-1346-5 · Cited by 1
A comprehensive map of the sequence basis of transcription initiation in humans
He, A. Y., Tian, C., & Kundaje, A. (2026) · bioRxiv · doi:10.64898/2026.10.29.762743
“…accessibility is confounded when both positive and negative training examples are drawn from accessible chromatin, and secondarily because shallow sequencing depth causes disproportionate dropout of the lowly transcribed enhancers that GATA1 predominantly binds [27] (Supplementary Note 1).”
Ryder: Epigenome normalization using a two-tier model and internal reference regions.
Cao, Y.-Q., Ge, G.-Z., & Zhao, K.-J. (2026) · Bioinformatics · doi:10.1093/bioinformatics/btag753
“…we found that inhibition of BRG1 using a chemical inhibitor, BRM014, resulted in increased nucleosome occupancy at enhancer centers and decreased occupancy in flanking regions, consistent with our previous finding that BRG1 acts to maintain a nucleosome-free region at enhancers ( 31, 34 ).”
Self-citationLi, X., & Eisen, M. B. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.23.707495
Turpin, M., Madigou, T., Bizot, M., Acker, R., Avner, S., Benoît, G., Braud, M., Fourgeux, C., Palierne, G., Poschmann, J., et al. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag152
“The size of this nucleosome-shift effect is very reminiscent of that observed upon alterations in the activity of chromatin re-modelers such as BRG1 [ 100 , 101 ].”
ASCL1 interacts with the mSWI/SNF at distal regulatory elements to regulate neural differentiationPreprint
Păun, O., Tan, Y. X., Patel, H., Strohbuecker, S., Ghanate, A. D., Gigli, C. C., Sopeña, M. L., Gerontogianni, L., Goldstone, R. J., Ang, S., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.09.510609 · Cited by 2
“, 2020), and/or interaction with other transcription factors and proteins with chromatin remodeling capacity (Hu et al., 2011; King and Klose, 2017; Takaku et al., 2016; Theodorou et al., 2013; Wang et al., 2014).”
BackgroundInfluentialBRG1 promotes transcriptional patterns that are permissive to proliferation in cancer cells
Giles, K., Gould, C. M., Achinger-Kawecka, J., Page, S. G., Kafer, G., Luu, P.-L., Cesare, A. J., Clark, S., & Taberlay, P. (2020) · bioRxiv · doi:10.1101/2020.07.03.187385
PBAP chromatin remodeler mediates enhancer-driven transcription in DrosophilaPreprint
Shidlovskii, Y., Shaposhnikov, A., Bylino, O. V., Amendola, D., Simone, G. D., Afeltra, N., Schedl, P., Digilio, F. A., & Giordano, E. (2020) · bioRxiv · doi:10.1101/2020.04.11.036772
“SWI/S NF similarly establishes the nucleosome landscape on enhancers [44, 49], and its participation in local histone acetylation has also been described [42].”
BackgroundCharacterizing higher order structures of chromatin in human cells
Schwartz, U., Németh, A., Diermeier, S., Exler, J. H., Hansch, S., Maldonado, R., Heizinger, L., Merkl, R., & Läengst, G. (2018) · bioRxiv · doi:10.1101/267856
Sefrioui, D. (2017) · doi:10.70675/58257576zef53z49b3zb16bz3309b1154d62
“Plusieurs travaux ont montré que le positionnement des nucléosomes variait en fonction de différentes conditions tissulaires physiologiques ou pathologiques (Schones et al, 2008; Hu et al, 2011; Valouev et al, 2011; Gaffney et al, 2012).”
BackgroundPetiti, L. (2015) · Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) · doi:10.13130/petiti-luca_phd2015-07-01
The Control of Gene Expression in Macrophages
Ostuni, R., & Natoli, G. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1311-4_26
Griffith, A. (2016) · uO Research (University of Ottawa) · doi:10.20381/ruor-849
“From the hematopoietic lineage HSCs [50, 54, 55], Erythroid [56, 57, 58], Megakaryocyte [59], and T-ALL cell lines and primary cells [39, 56] were contributed.”
BackgroundBarutcu, A. R. (2016) · eScholarship@UMassChan · doi:10.13028/m2t01z
“[247; 248] and B-cells [245] and colocalizes with pluripotency factors [249], suggesting”
Background
Metadata
- Authors
- Hu, G., Schones, D. E., Cui, K., Ybarra, R., Northrup, D., Tang, Q., Gattinoni, L., Restifo, N. P., Huang, S., & Zhao, K.
- Affiliations
- National Institutes of Health (US)
- University of Florida Health (US)
- ORCID
- Venue
- Genome Research
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2011-07-27
- Volume
- 21
- Issue
- 10
- Pages
- 1650-1658
- ISSN
- 1088-9051 (ISSN-L)
- PMC
- PMC3202282
- OpenAlex
- W2119037385
- Cited by
- 186
- References
- 0
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 6 · 2023: 4 · 2022: 10 · 2021: 19 · 2020: 12 · 2019: 14 · 2018: 15 · 2017: 11 · 2016: 18 · 2015: 11 · 2014: 25 · 2013: 15 · 2012: 16
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genome Research (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- National Institutes of Health
- National Heart, Lung, and Blood Institute (R01HL091929, K22HL101950, R01HL090589)
- NHLBI Division of Intramural Research
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- SMARCA4, BAF chromatin remodeling complex, nucleosome positioning, enhancers, GATA-1, TAL1, hematopoietic stem cell differentiation, erythropoiesis, transcription factor binding, chromatin regulation
- MeSH terms
- T-Cell Acute Lymphocytic Leukemia Protein 1, CCCTC-Binding Factor, Binding Sites, Cell Differentiation, Cells, Cultured, DNA Helicases, Enhancer Elements, Genetic, Gene Expression Regulation, Hematopoiesis, Hematopoietic Stem Cells, Humans, Nuclear Proteins, Nucleosomes, Organ Specificity, Proto-Oncogene Proteins, Repressor Proteins, Transcription Factors, Transcription, Genetic, Chromatin Assembly and Disassembly, Chromatin Immunoprecipitation, GATA1 Transcription Factor, Basic Helix-Loop-Helix Proteins, Primary Cell Culture
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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