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Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites

The heterochromatin environment plays a central role in silencing genes associated with the malaria parasite’s development, survival in the host, and transmission to the mosquito vector. However, the underlying mechanism regulating the dynamic chromatin structure is not understood yet. Here, we have...

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Autores principales: Fan, Yanting, Shen, Shijun, Wei, Guiying, Tang, Jianxia, Zhao, Yuemeng, Wang, Fei, He, Xiaohui, Guo, Gangqiang, Shang, Xiaomin, Yu, Xinyu, Ma, Zhenlin, He, Xiaoqin, Liu, Meng, Zhu, Qianshu, Le, Zhen, Wei, Gang, Cao, Jun, Jiang, Cizhong, Zhang, Qingfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267889/
https://www.ncbi.nlm.nih.gov/pubmed/32487761
http://dx.doi.org/10.1128/mBio.01110-20
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author Fan, Yanting
Shen, Shijun
Wei, Guiying
Tang, Jianxia
Zhao, Yuemeng
Wang, Fei
He, Xiaohui
Guo, Gangqiang
Shang, Xiaomin
Yu, Xinyu
Ma, Zhenlin
He, Xiaoqin
Liu, Meng
Zhu, Qianshu
Le, Zhen
Wei, Gang
Cao, Jun
Jiang, Cizhong
Zhang, Qingfeng
author_facet Fan, Yanting
Shen, Shijun
Wei, Guiying
Tang, Jianxia
Zhao, Yuemeng
Wang, Fei
He, Xiaohui
Guo, Gangqiang
Shang, Xiaomin
Yu, Xinyu
Ma, Zhenlin
He, Xiaoqin
Liu, Meng
Zhu, Qianshu
Le, Zhen
Wei, Gang
Cao, Jun
Jiang, Cizhong
Zhang, Qingfeng
author_sort Fan, Yanting
collection PubMed
description The heterochromatin environment plays a central role in silencing genes associated with the malaria parasite’s development, survival in the host, and transmission to the mosquito vector. However, the underlying mechanism regulating the dynamic chromatin structure is not understood yet. Here, we have uncovered that Plasmodium falciparum Rrp6, an orthologue of eukaryotic RNA exosome-associated RNase, controls the silencing of heterochromatic genes. PfRrp6 knockdown disrupted the singular expression of the GC-rich ncRNA RUF6 family, a known critical regulator of virulence gene expression, through the stabilization of the nascent transcripts. Mechanistic investigation showed that the accumulation of the multiple RUF6 ncRNAs triggered local chromatin remodeling in situ, which activated their adjacent var genes. Strikingly, chromatin isolation by RNA purification analysis (ChIRP-seq) revealed that a remarkable RUF6 ncRNA had interacted with distal heterochromatin regions directly and stimulated a global derepression effect on heterochromatic genes, including all variant gene families and the sexual commitment-associated regulator ap2-g gene. Collectively, Rrp6 appears to conduct the epigenetic surveillance of heterochromatic gene expression through controlling RUF6 levels, thereby securing antigenic variation and sexual commitment of malaria parasites during the infection of the host.
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spelling pubmed-72678892020-06-08 Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites Fan, Yanting Shen, Shijun Wei, Guiying Tang, Jianxia Zhao, Yuemeng Wang, Fei He, Xiaohui Guo, Gangqiang Shang, Xiaomin Yu, Xinyu Ma, Zhenlin He, Xiaoqin Liu, Meng Zhu, Qianshu Le, Zhen Wei, Gang Cao, Jun Jiang, Cizhong Zhang, Qingfeng mBio Research Article The heterochromatin environment plays a central role in silencing genes associated with the malaria parasite’s development, survival in the host, and transmission to the mosquito vector. However, the underlying mechanism regulating the dynamic chromatin structure is not understood yet. Here, we have uncovered that Plasmodium falciparum Rrp6, an orthologue of eukaryotic RNA exosome-associated RNase, controls the silencing of heterochromatic genes. PfRrp6 knockdown disrupted the singular expression of the GC-rich ncRNA RUF6 family, a known critical regulator of virulence gene expression, through the stabilization of the nascent transcripts. Mechanistic investigation showed that the accumulation of the multiple RUF6 ncRNAs triggered local chromatin remodeling in situ, which activated their adjacent var genes. Strikingly, chromatin isolation by RNA purification analysis (ChIRP-seq) revealed that a remarkable RUF6 ncRNA had interacted with distal heterochromatin regions directly and stimulated a global derepression effect on heterochromatic genes, including all variant gene families and the sexual commitment-associated regulator ap2-g gene. Collectively, Rrp6 appears to conduct the epigenetic surveillance of heterochromatic gene expression through controlling RUF6 levels, thereby securing antigenic variation and sexual commitment of malaria parasites during the infection of the host. American Society for Microbiology 2020-06-02 /pmc/articles/PMC7267889/ /pubmed/32487761 http://dx.doi.org/10.1128/mBio.01110-20 Text en Copyright © 2020 Fan et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Fan, Yanting
Shen, Shijun
Wei, Guiying
Tang, Jianxia
Zhao, Yuemeng
Wang, Fei
He, Xiaohui
Guo, Gangqiang
Shang, Xiaomin
Yu, Xinyu
Ma, Zhenlin
He, Xiaoqin
Liu, Meng
Zhu, Qianshu
Le, Zhen
Wei, Gang
Cao, Jun
Jiang, Cizhong
Zhang, Qingfeng
Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites
title Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites
title_full Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites
title_fullStr Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites
title_full_unstemmed Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites
title_short Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites
title_sort rrp6 regulates heterochromatic gene silencing via ncrna ruf6 decay in malaria parasites
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267889/
https://www.ncbi.nlm.nih.gov/pubmed/32487761
http://dx.doi.org/10.1128/mBio.01110-20
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