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C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association
Jumonji C (JmjC) domain-containing protein 14 (JMJ14) is an H3K4-specific histone demethylase that has important roles in RNA-mediated gene silencing and flowering time regulation in Arabidopsis. However, how JMJ14 is recruited to its target genes remains unclear. Here, we show that the C-terminal F...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659397/ https://www.ncbi.nlm.nih.gov/pubmed/26617990 http://dx.doi.org/10.1038/celldisc.2015.3 |
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author | Zhang, Shuaibin Zhou, Bing Kang, Yanyuan Cui, Xia Liu, Ao Deleris, Angelique Greenberg, Maxim VC Cui, Xiekui Qiu, Qi Lu, Falong Wohlschlegel, James A Jacobsen, Steven E Cao, Xiaofeng |
author_facet | Zhang, Shuaibin Zhou, Bing Kang, Yanyuan Cui, Xia Liu, Ao Deleris, Angelique Greenberg, Maxim VC Cui, Xiekui Qiu, Qi Lu, Falong Wohlschlegel, James A Jacobsen, Steven E Cao, Xiaofeng |
author_sort | Zhang, Shuaibin |
collection | PubMed |
description | Jumonji C (JmjC) domain-containing protein 14 (JMJ14) is an H3K4-specific histone demethylase that has important roles in RNA-mediated gene silencing and flowering time regulation in Arabidopsis. However, how JMJ14 is recruited to its target genes remains unclear. Here, we show that the C-terminal FYRN (F/Y-rich N terminus) and FYRC (F/Y-rich C terminus) domains of JMJ14 are required for RNA silencing and flowering time regulation. Chromatin binding of JMJ14 is lost upon deletion of its FYRN and FYRC domains, and H3K4me3 is increased. FYRN and FYRC domains interact with a pair of NAC (NAM, ATAF, CUC) domain-containing transcription factors, NAC050 and NAC052. Genome-wide chromatin immunoprecipitation analysis revealed that JMJ14 and NAC050/052 share a set of common target genes with CTTGNNNNNCAAG consensus sequences. Mutations in either NAC052 or NAC050 impair RNA-mediated gene silencing. Together, our findings demonstrate an important role of FYRN and FYRC domains in targeting JMJ14 through direct interaction with NAC050/052 proteins, which reveals a novel mechanism of histone demethylase recruitment. |
format | Online Article Text |
id | pubmed-4659397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46593972016-04-28 C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association Zhang, Shuaibin Zhou, Bing Kang, Yanyuan Cui, Xia Liu, Ao Deleris, Angelique Greenberg, Maxim VC Cui, Xiekui Qiu, Qi Lu, Falong Wohlschlegel, James A Jacobsen, Steven E Cao, Xiaofeng Cell Discov Article Jumonji C (JmjC) domain-containing protein 14 (JMJ14) is an H3K4-specific histone demethylase that has important roles in RNA-mediated gene silencing and flowering time regulation in Arabidopsis. However, how JMJ14 is recruited to its target genes remains unclear. Here, we show that the C-terminal FYRN (F/Y-rich N terminus) and FYRC (F/Y-rich C terminus) domains of JMJ14 are required for RNA silencing and flowering time regulation. Chromatin binding of JMJ14 is lost upon deletion of its FYRN and FYRC domains, and H3K4me3 is increased. FYRN and FYRC domains interact with a pair of NAC (NAM, ATAF, CUC) domain-containing transcription factors, NAC050 and NAC052. Genome-wide chromatin immunoprecipitation analysis revealed that JMJ14 and NAC050/052 share a set of common target genes with CTTGNNNNNCAAG consensus sequences. Mutations in either NAC052 or NAC050 impair RNA-mediated gene silencing. Together, our findings demonstrate an important role of FYRN and FYRC domains in targeting JMJ14 through direct interaction with NAC050/052 proteins, which reveals a novel mechanism of histone demethylase recruitment. Nature Publishing Group 2015-04-28 /pmc/articles/PMC4659397/ /pubmed/26617990 http://dx.doi.org/10.1038/celldisc.2015.3 Text en Copyright © 2015 SIBS, CAS http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Zhang, Shuaibin Zhou, Bing Kang, Yanyuan Cui, Xia Liu, Ao Deleris, Angelique Greenberg, Maxim VC Cui, Xiekui Qiu, Qi Lu, Falong Wohlschlegel, James A Jacobsen, Steven E Cao, Xiaofeng C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association |
title | C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association |
title_full | C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association |
title_fullStr | C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association |
title_full_unstemmed | C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association |
title_short | C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association |
title_sort | c-terminal domains of histone demethylase jmj14 interact with a pair of nac transcription factors to mediate specific chromatin association |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659397/ https://www.ncbi.nlm.nih.gov/pubmed/26617990 http://dx.doi.org/10.1038/celldisc.2015.3 |
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