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Structure, activity and function of the lysine methyltransferase SETD5

SET domain-containing 5 (SETD5) is an uncharacterized member of the protein lysine methyltransferase family and is best known for its transcription machinery by methylating histone H3 on lysine 36 (H3K36). These well-characterized functions of SETD5 are transcription regulation, euchromatin formatio...

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Autores principales: Li, Mingyang, Hou, Yanan, Zhang, Ziwei, Zhang, Bowen, Huang, Ting, Sun, Aiqin, Shao, Genbao, Lin, Qiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982096/
https://www.ncbi.nlm.nih.gov/pubmed/36875494
http://dx.doi.org/10.3389/fendo.2023.1089527
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author Li, Mingyang
Hou, Yanan
Zhang, Ziwei
Zhang, Bowen
Huang, Ting
Sun, Aiqin
Shao, Genbao
Lin, Qiong
author_facet Li, Mingyang
Hou, Yanan
Zhang, Ziwei
Zhang, Bowen
Huang, Ting
Sun, Aiqin
Shao, Genbao
Lin, Qiong
author_sort Li, Mingyang
collection PubMed
description SET domain-containing 5 (SETD5) is an uncharacterized member of the protein lysine methyltransferase family and is best known for its transcription machinery by methylating histone H3 on lysine 36 (H3K36). These well-characterized functions of SETD5 are transcription regulation, euchromatin formation, and RNA elongation and splicing. SETD5 is frequently mutated and hyperactive in both human neurodevelopmental disorders and cancer, and could be down-regulated by degradation through the ubiquitin-proteasome pathway, but the biochemical mechanisms underlying such dysregulation are rarely understood. Herein, we provide an update on the particularities of SETD5 enzymatic activity and substrate specificity concerning its biological importance, as well as its molecular and cellular impact on normal physiology and disease, with potential therapeutic options.
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spelling pubmed-99820962023-03-04 Structure, activity and function of the lysine methyltransferase SETD5 Li, Mingyang Hou, Yanan Zhang, Ziwei Zhang, Bowen Huang, Ting Sun, Aiqin Shao, Genbao Lin, Qiong Front Endocrinol (Lausanne) Endocrinology SET domain-containing 5 (SETD5) is an uncharacterized member of the protein lysine methyltransferase family and is best known for its transcription machinery by methylating histone H3 on lysine 36 (H3K36). These well-characterized functions of SETD5 are transcription regulation, euchromatin formation, and RNA elongation and splicing. SETD5 is frequently mutated and hyperactive in both human neurodevelopmental disorders and cancer, and could be down-regulated by degradation through the ubiquitin-proteasome pathway, but the biochemical mechanisms underlying such dysregulation are rarely understood. Herein, we provide an update on the particularities of SETD5 enzymatic activity and substrate specificity concerning its biological importance, as well as its molecular and cellular impact on normal physiology and disease, with potential therapeutic options. Frontiers Media S.A. 2023-02-17 /pmc/articles/PMC9982096/ /pubmed/36875494 http://dx.doi.org/10.3389/fendo.2023.1089527 Text en Copyright © 2023 Li, Hou, Zhang, Zhang, Huang, Sun, Shao and Lin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Li, Mingyang
Hou, Yanan
Zhang, Ziwei
Zhang, Bowen
Huang, Ting
Sun, Aiqin
Shao, Genbao
Lin, Qiong
Structure, activity and function of the lysine methyltransferase SETD5
title Structure, activity and function of the lysine methyltransferase SETD5
title_full Structure, activity and function of the lysine methyltransferase SETD5
title_fullStr Structure, activity and function of the lysine methyltransferase SETD5
title_full_unstemmed Structure, activity and function of the lysine methyltransferase SETD5
title_short Structure, activity and function of the lysine methyltransferase SETD5
title_sort structure, activity and function of the lysine methyltransferase setd5
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982096/
https://www.ncbi.nlm.nih.gov/pubmed/36875494
http://dx.doi.org/10.3389/fendo.2023.1089527
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