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19S蛋白酶体调控裂殖酵母中的亚端粒沉默和兼性异染色质形成。

The 19S proteasome regulates subtelomere silencing and facultative heterochromatin formation in fission yeast.

作者信息

Seo Hogyu David, Kwon Chang Seob, Lee Daeyoup

机构信息

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, 34141, South Korea.

Department of Chemistry and Biology, Korea Science Academy of KAIST, Busan, 47162, South Korea.

出版信息

Curr Genet. 2018 Jun;64(3):741-752. doi: 10.1007/s00294-017-0792-6. Epub 2017 Dec 6.

Abstract

Accumulating evidence shows that non-proteolytic functions of the proteasome are as crucial as its well-known proteolytic function in regulating cellular activities. In our recent work, we showed that the 19S proteasome mediates the heterochromatin spreading of centromeric heterochromatin in non-proteolytic manner. However, the involvement of the proteasome in other heterochromatin regions remained largely unknown. In the present study, we investigated the non-proteolytic role of the 19S proteasome in subtelomere and facultative heterochromatin regions. Using the non-proteolytic mutant, rpt4-1, we show that the 19S proteasome is involved in regulating subtelomere silencing and facultative heterochromatin formation in fission yeast. In addition to this proteasome-related regulation, we also observed a distinct pathway that regulates subtelomere silencing and facultative heterochromatin formation through the Paf1 complex subunit, Leo1. Our comparison of the two pathways revealed a new group of heterochromatin domains that are regulated exclusively by the proteasome pathway. Taken together, our findings reveal that the proteasome is involved in the global regulation of facultative and constitutive heterochromatin.

摘要

越来越多的证据表明,蛋白酶体的非蛋白水解功能在调节细胞活动中与其广为人知的蛋白水解功能同样重要。在我们最近的研究中,我们发现19S蛋白酶体以非蛋白水解方式介导着丝粒异染色质的异染色质扩展。然而,蛋白酶体在其他异染色质区域的作用在很大程度上仍不清楚。在本研究中,我们调查了19S蛋白酶体在亚端粒和兼性异染色质区域的非蛋白水解作用。使用非蛋白水解突变体rpt4-1,我们发现19S蛋白酶体参与调节裂殖酵母中的亚端粒沉默和兼性异染色质形成。除了这种与蛋白酶体相关的调节外,我们还观察到一条通过Paf1复合物亚基Leo1调节亚端粒沉默和兼性异染色质形成的独特途径。我们对这两条途径的比较揭示了一组仅由蛋白酶体途径调节的新的异染色质结构域。综上所述,我们的研究结果表明蛋白酶体参与了兼性和组成型异染色质的全局调节。

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