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

ABSTRACT 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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Yanting Fan, Shijun Shen, Guiying Wei, Jianxia Tang, Yuemeng Zhao, Fei Wang, Xiaohui He, Gangqiang Guo, Xiaomin Shang, Xinyu Yu, Zhenlin Ma, Xiaoqin He, Meng Liu, Qianshu Zhu, Zhen Le, Gang Wei, Jun Cao, Cizhong Jiang, Qingfeng Zhang
Formato: article
Lenguaje:EN
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://doaj.org/article/9cab13a866c54338aa2778af35f5f676
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:9cab13a866c54338aa2778af35f5f676
record_format dspace
spelling oai:doaj.org-article:9cab13a866c54338aa2778af35f5f6762021-11-15T15:56:46ZRrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites10.1128/mBio.01110-202150-7511https://doaj.org/article/9cab13a866c54338aa2778af35f5f6762020-06-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01110-20https://doaj.org/toc/2150-7511ABSTRACT 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. IMPORTANCE Malaria remains a major public health and economic burden. The heterochromatin environment controls the silencing of genes associated with the fate of malaria parasites. Previous studies have demonstrated that a group of GC-rich ncRNAs (RUF6) is associated with the mutually exclusive expression of var genes, but the underlying mechanisms remain elusive. Here, through a series of genetic manipulation and genome-wide multiomics analysis, we have identified the plasmodial orthologue of RNA exosome-associated Rrp6 as an upstream regulator of RUF6 expression and revealed that the dysregulation of RUF6 upon Rrp6 knockdown triggered local chromatin alteration, thereby activating most heterochromatic genes via direct interaction of RUF6 and distal gene loci. This finding not only uncovered the in-depth mechanism of RUF6-mediated regulation of heterochromatic genes but also identified Rrp6 as a novel regulator of gene expression in human malaria parasites, which provides a new target for developing intervention strategies against malaria.Yanting FanShijun ShenGuiying WeiJianxia TangYuemeng ZhaoFei WangXiaohui HeGangqiang GuoXiaomin ShangXinyu YuZhenlin MaXiaoqin HeMeng LiuQianshu ZhuZhen LeGang WeiJun CaoCizhong JiangQingfeng ZhangAmerican Society for MicrobiologyarticleRNA exosomemalariaheterochromatingene regulationncRNAMicrobiologyQR1-502ENmBio, Vol 11, Iss 3 (2020)
institution DOAJ
collection DOAJ
language EN
topic RNA exosome
malaria
heterochromatin
gene regulation
ncRNA
Microbiology
QR1-502
spellingShingle RNA exosome
malaria
heterochromatin
gene regulation
ncRNA
Microbiology
QR1-502
Yanting Fan
Shijun Shen
Guiying Wei
Jianxia Tang
Yuemeng Zhao
Fei Wang
Xiaohui He
Gangqiang Guo
Xiaomin Shang
Xinyu Yu
Zhenlin Ma
Xiaoqin He
Meng Liu
Qianshu Zhu
Zhen Le
Gang Wei
Jun Cao
Cizhong Jiang
Qingfeng Zhang
Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites
description ABSTRACT 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. IMPORTANCE Malaria remains a major public health and economic burden. The heterochromatin environment controls the silencing of genes associated with the fate of malaria parasites. Previous studies have demonstrated that a group of GC-rich ncRNAs (RUF6) is associated with the mutually exclusive expression of var genes, but the underlying mechanisms remain elusive. Here, through a series of genetic manipulation and genome-wide multiomics analysis, we have identified the plasmodial orthologue of RNA exosome-associated Rrp6 as an upstream regulator of RUF6 expression and revealed that the dysregulation of RUF6 upon Rrp6 knockdown triggered local chromatin alteration, thereby activating most heterochromatic genes via direct interaction of RUF6 and distal gene loci. This finding not only uncovered the in-depth mechanism of RUF6-mediated regulation of heterochromatic genes but also identified Rrp6 as a novel regulator of gene expression in human malaria parasites, which provides a new target for developing intervention strategies against malaria.
format article
author Yanting Fan
Shijun Shen
Guiying Wei
Jianxia Tang
Yuemeng Zhao
Fei Wang
Xiaohui He
Gangqiang Guo
Xiaomin Shang
Xinyu Yu
Zhenlin Ma
Xiaoqin He
Meng Liu
Qianshu Zhu
Zhen Le
Gang Wei
Jun Cao
Cizhong Jiang
Qingfeng Zhang
author_facet Yanting Fan
Shijun Shen
Guiying Wei
Jianxia Tang
Yuemeng Zhao
Fei Wang
Xiaohui He
Gangqiang Guo
Xiaomin Shang
Xinyu Yu
Zhenlin Ma
Xiaoqin He
Meng Liu
Qianshu Zhu
Zhen Le
Gang Wei
Jun Cao
Cizhong Jiang
Qingfeng Zhang
author_sort Yanting Fan
title 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_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_sort rrp6 regulates heterochromatic gene silencing via ncrna ruf6 decay in malaria parasites
publisher American Society for Microbiology
publishDate 2020
url https://doaj.org/article/9cab13a866c54338aa2778af35f5f676
work_keys_str_mv AT yantingfan rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT shijunshen rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT guiyingwei rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT jianxiatang rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT yuemengzhao rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT feiwang rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT xiaohuihe rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT gangqiangguo rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT xiaominshang rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT xinyuyu rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT zhenlinma rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT xiaoqinhe rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT mengliu rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT qianshuzhu rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT zhenle rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT gangwei rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT juncao rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT cizhongjiang rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
AT qingfengzhang rrp6regulatesheterochromaticgenesilencingviancrnaruf6decayinmalariaparasites
_version_ 1718427107936174080