RING1 missense variants reveal sensitivity of DNA damage repair to H2A monoubiquitination dosage during neurogenesis-Reference-Cited by-同舟云学术

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RING1 missense variants reveal sensitivity of DNA damage repair to H2A monoubiquitination dosage during neurogenesis

Published:2024-09-10 Issue:1 Volume:15 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Ryan C. W.^ORCID,Regan S. L.,Mills E. F.,McGrath B. T.,Gong E.,Lai Y. T.,Sheingold J. B.,Patel K.^ORCID,Horowitz T.,Moccia A.^ORCID,Tsan Y. C.,Srivastava A.,Bielas S. L.^ORCID

Funder

U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development

U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s41467-024-52292-8.pdf

Reference77 articles.

1. Barbour, H. et al. Polycomb group-mediated histone H2A monoubiquitination in epigenome regulation and nuclear processes. Nat. Commun. 11, 5947 (2020).

2. Illingworth, R. S. et al. The E3 ubiquitin ligase activity of RING1B is not essential for early mouse development. Genes Dev. 29, 1897–1902 (2015).

3. Blackledge, N. P. et al. PRC1 catalytic activity is central to polycomb system function. Mol. Cell 77, 857–874.e9 (2020).

4. del Mar Lorente, M. et al. Loss- and gain-of-function mutations show a polycomb group function for Ring1A in mice. Development 127, 5093–5100 (2000).

5. Eskeland, R. et al. Ring1B compacts chromatin structure and represses gene expression independent of histone ubiquitination. Mol. Cell 38, 452–464 (2010).

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