[SNG2]是Cut4/Apc1的一种朊病毒形式,它使裂殖酵母的异染色质沉默缺陷具有非孟德尔遗传性

IF 16.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Suman Sharma, Suchita Srivastava, Rudra Narayan Dubey, Poonam Mishra, Jagmohan Singh
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引用次数: 0

摘要

朊病毒代表着表观遗传调节蛋白,它们可以自我传播其结构,并将其错误折叠的结构和功能赋予正常折叠的蛋白质。与哺乳动物的朊病毒 PrPSc 一样,真菌中也存在朊病毒。虽然少数朊病毒(如 Swi1)会影响基因表达,但没有任何朊病毒会影响异染色质的结构和功能。在裂殖酵母和类囊动物中,组蛋白甲基转移酶Clr4/Suv39会导致H3-Lys9甲基化,而H3-Lys9会与染色质链蛋白Swi6/HP1结合,从而形成异染色质。早些时候,我们发现无性繁殖促进复合体Cut4亚基的sng2-1突变由于Swi6的结合和招募缺陷而导致异染色质结构失效。在这里,我们证明了 Cut4p 形成了一种非经典的朊病毒形式,命名为 [SNG2],它能终止异染色质沉默。[SNG2]具有多种朊病毒样特性,如非孟德尔遗传、其传播需要 Hsp 蛋白、cut4 过表达时从头生成、胍类可逆固化、胞质遗传和形成感染性蛋白聚集体,这些聚集体在过表达 hsp 基因时被溶解。有趣的是,[SNG2]朊病毒增强了对应激条件的耐受性,这支持了它在进化过程中促进细胞在环境压力下生存的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[SNG2], a prion form of Cut4/Apc1, confers non-Mendelian inheritance of heterochromatin silencing defect in fission yeast
Prions represent epigenetic regulator proteins that can self-propagate their structure and confer their misfolded structure and function on normally folded proteins. Like the mammalian prion PrPSc, prions also occur in fungi. While a few prions, like Swi1, affect gene expression, none are shown to affect heterochromatin structure and function. In fission yeast and metazoans, histone methyltransferase Clr4/Suv39 causes H3-Lys9 methylation, which is bound by the chromodomain protein Swi6/HP1 to assemble heterochromatin. Earlier, we showed that sng2-1 mutation in the Cut4 subunit of anaphase-promoting complex abrogates heterochromatin structure due to defective binding and recruitment of Swi6. Here, we demonstrate that the Cut4p forms a non-canonical prion form, designated as [SNG2], which abrogates heterochromatin silencing. [SNG2] exhibits various prion-like properties, e.g. non-Mendelian inheritance, requirement of Hsp proteins for its propagation, de novo generation upon cut4 overexpression, reversible curing by guanidine, cytoplasmic inheritance and formation of infectious protein aggregates, which are dissolved upon overexpression of hsp genes. Interestingly, [SNG2] prion imparts an enhanced tolerance to stress conditions, supporting its role in promoting cell survival under environmental stress during evolution.
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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