Histone Ubiquitination: An Integrative Signaling Platform in Genome Stability

Complex mechanisms are in place to maintain genome stability. Ubiquitination of chromatin plays a central role in these mechanisms. The ever-growing complexity of the ubiquitin (Ub) code and of chromatin modifications and dynamics challenges our ability to fully understand how histone ubiquitination...

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Vydané v:Trends in genetics Ročník 37; číslo 6; s. 566 - 581
Hlavní autori: Mattiroli, Francesca, Penengo, Lorenza
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England Elsevier Ltd 01.06.2021
Predmet:
chromatin modifications
DDR
DNA damage response
H2AK15ub
pUbT12
RNF8/RNF168/USP51
ubiquitin phosphorylation
pUbT12
DDR
DNA damage response
ubiquitin phosphorylation
chromatin modifications
H2AK15ub
RNF8/RNF168/USP51
ISSN:0168-9525
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Shrnutí:Complex mechanisms are in place to maintain genome stability. Ubiquitination of chromatin plays a central role in these mechanisms. The ever-growing complexity of the ubiquitin (Ub) code and of chromatin modifications and dynamics challenges our ability to fully understand how histone ubiquitination regulates genome stability. Here we review the current knowledge on specific, low-abundant histone ubiquitination events that are highly regulated within the cellular DNA damage response (DDR), with particular emphasis on the latest discovery of Ub phosphorylation as a novel regulator of the DDR signaling pathway. We discuss players involved and potential implications of histone (phospho)ubiquitination on chromatin structure, and we highlight exciting open questions for future research. Histones are heavily post-translationally modified by ubiquitin. Lately, many more ubiquitin-based modifications have been mapped on histones, which are far less abundant than the canonical ones but essential to safeguard genome stability.Histones at damaged DNA can be modified by phospho-ubiquitin (i.e., pUb at Thr12), resulting in chromatin regions with new properties that impact DNA repair pathways.The discovery of new ubiquitination sites on histones and new ubiquitin modifications expands dramatically the landscape of chromatin-based signaling and crosstalk, paving the way for future studies on novel mechanisms in genome stability programs (i.e., new writers, readers, and erasers).
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ISSN:0168-9525
DOI:10.1016/j.tig.2020.12.005