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CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiation
| dc.date.accessioned | 2021-10-27T19:57:29Z | |
| dc.date.available | 2021-10-27T19:57:29Z | |
| dc.date.issued | 2020 | |
| dc.identifier.uri | https://hdl.handle.net/1721.1/133981 | |
| dc.description.abstract | © 2020 National Academy of Sciences. All rights reserved. Hematopoietic stem and progenitor cell (HSPC) formation and lineage differentiation involve gene expression programs orchestrated by transcription factors and epigenetic regulators. Genetic disruption of the chromatin remodeler chromodomain-helicase-DNA-binding protein 7 (CHD7) expanded phenotypic HSPCs, erythroid, and myeloid lineages in zebrafish and mouse embryos. CHD7 acts to suppress hematopoietic differentiation. Binding motifs for RUNX and other hematopoietic transcription factors are enriched at sites occupied by CHD7, and decreased RUNX1 occupancy correlated with loss of CHD7 localization. CHD7 physically interacts with RUNX1 and suppresses RUNX1-induced expansion of HSPCs during development through modulation of RUNX1 activity. Consequently, the RUNX1:CHD7 axis provides proper timing and function of HSPCs as they emerge during hematopoietic development or mature in adults, representing a distinct and evolutionarily conserved control mechanism to ensure accurate hematopoietic lineage differentiation. | |
| dc.language.iso | en | |
| dc.publisher | Proceedings of the National Academy of Sciences | |
| dc.relation.isversionof | 10.1073/PNAS.2003228117 | |
| dc.rights | Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. | |
| dc.source | PNAS | |
| dc.title | CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiation | |
| dc.type | Article | |
| dc.relation.journal | Proceedings of the National Academy of Sciences of the United States of America | |
| dc.eprint.version | Final published version | |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | |
| dc.date.updated | 2021-08-04T18:50:00Z | |
| dspace.orderedauthors | Hsu, J; Huang, H-T; Lee, C-T; Choudhuri, A; Wilson, NK; Abraham, BJ; Moignard, V; Kucinski, I; Yu, S; Hyde, RK; Tober, J; Cai, X; Li, Y; Guo, Y; Yang, S; Superdock, M; Trompouki, E; Calero-Nieto, FJ; Ghamari, A; Jiang, J; Gao, P; Gao, L; Nguyen, V; Robertson, AL; Durand, EM; Kathrein, KL; Aifantis, I; Gerber, SA; Tong, W; Tan, K; Cantor, AB; Zhou, Y; Liu, PP; Young, RA; Göttgens, B; Speck, NA; Zon, LI | |
| dspace.date.submission | 2021-08-04T18:50:02Z | |
| mit.journal.volume | 117 | |
| mit.journal.issue | 38 | |
| mit.license | PUBLISHER_POLICY | |
| mit.metadata.status | Authority Work and Publication Information Needed |
