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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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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. |
format | Online Article Text |
id | pubmed-9982096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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