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...
Guardado en:
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
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 |