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HDAC1 SUMOylation promotes Argonaute-directed transcriptional silencing in C. elegans

Eukaryotic cells use guided search to coordinately control dispersed genetic elements. Argonaute proteins and their small RNA cofactors engage nascent RNAs and chromatin-associated proteins to direct transcriptional silencing. The small ubiquitin-like modifier (SUMO) has been shown to promote the fo...

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Autores principales: Kim, Heesun, Ding, Yue-He, Zhang, Gangming, Yan, Yong-Hong, Conte, Darryl, Dong, Meng-Qiu, Mello, Craig C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131101/
https://www.ncbi.nlm.nih.gov/pubmed/34003109
http://dx.doi.org/10.7554/eLife.63299
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author Kim, Heesun
Ding, Yue-He
Zhang, Gangming
Yan, Yong-Hong
Conte, Darryl
Dong, Meng-Qiu
Mello, Craig C
author_facet Kim, Heesun
Ding, Yue-He
Zhang, Gangming
Yan, Yong-Hong
Conte, Darryl
Dong, Meng-Qiu
Mello, Craig C
author_sort Kim, Heesun
collection PubMed
description Eukaryotic cells use guided search to coordinately control dispersed genetic elements. Argonaute proteins and their small RNA cofactors engage nascent RNAs and chromatin-associated proteins to direct transcriptional silencing. The small ubiquitin-like modifier (SUMO) has been shown to promote the formation and maintenance of silent chromatin (called heterochromatin) in yeast, plants, and animals. Here, we show that Argonaute-directed transcriptional silencing in Caenorhabditis elegans requires SUMOylation of the type 1 histone deacetylase HDA-1. Our findings suggest how SUMOylation promotes the association of HDAC1 with chromatin remodeling factors and with a nuclear Argonaute to initiate de novo heterochromatin silencing.
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spelling pubmed-81311012021-05-19 HDAC1 SUMOylation promotes Argonaute-directed transcriptional silencing in C. elegans Kim, Heesun Ding, Yue-He Zhang, Gangming Yan, Yong-Hong Conte, Darryl Dong, Meng-Qiu Mello, Craig C eLife Developmental Biology Eukaryotic cells use guided search to coordinately control dispersed genetic elements. Argonaute proteins and their small RNA cofactors engage nascent RNAs and chromatin-associated proteins to direct transcriptional silencing. The small ubiquitin-like modifier (SUMO) has been shown to promote the formation and maintenance of silent chromatin (called heterochromatin) in yeast, plants, and animals. Here, we show that Argonaute-directed transcriptional silencing in Caenorhabditis elegans requires SUMOylation of the type 1 histone deacetylase HDA-1. Our findings suggest how SUMOylation promotes the association of HDAC1 with chromatin remodeling factors and with a nuclear Argonaute to initiate de novo heterochromatin silencing. eLife Sciences Publications, Ltd 2021-05-18 /pmc/articles/PMC8131101/ /pubmed/34003109 http://dx.doi.org/10.7554/eLife.63299 Text en © 2021, Kim et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Kim, Heesun
Ding, Yue-He
Zhang, Gangming
Yan, Yong-Hong
Conte, Darryl
Dong, Meng-Qiu
Mello, Craig C
HDAC1 SUMOylation promotes Argonaute-directed transcriptional silencing in C. elegans
title HDAC1 SUMOylation promotes Argonaute-directed transcriptional silencing in C. elegans
title_full HDAC1 SUMOylation promotes Argonaute-directed transcriptional silencing in C. elegans
title_fullStr HDAC1 SUMOylation promotes Argonaute-directed transcriptional silencing in C. elegans
title_full_unstemmed HDAC1 SUMOylation promotes Argonaute-directed transcriptional silencing in C. elegans
title_short HDAC1 SUMOylation promotes Argonaute-directed transcriptional silencing in C. elegans
title_sort hdac1 sumoylation promotes argonaute-directed transcriptional silencing in c. elegans
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8131101/
https://www.ncbi.nlm.nih.gov/pubmed/34003109
http://dx.doi.org/10.7554/eLife.63299
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