| Literature DB >> 27050457 |
Fu-ping Wen1,2, Yue-shuai Guo3, Yang Hu1,4, Wei-xiao Liu1, Qian Wang1,2, Yuan-ting Wang1,2, Hai-Yan Yu1,2, Chao-ming Tang1,2, Jun Yang4, Tao Zhou3, Zhi-ping Xie5, Jia-hao Sha3, Xuejiang Guo3, Wei Li1.
Abstract
Meiosis is a special type of cellular renovation that involves 2 successive cell divisions and a single round of DNA replication. Two major degradation systems, the autophagy-lysosome and the ubiquitin-proteasome, are involved in meiosis, but their roles have yet to be elucidated. Here we show that autophagy mainly affects the initiation of meiosis but not the nuclear division. Autophagy works not only by serving as a dynamic recycling system but also by eliminating some negative meiotic regulators such as Ego4 (Ynr034w-a). In a quantitative proteomics study, the proteasome was found to be significantly upregulated during meiotic divisions. We found that proteasomal activity is essential to the 2 successive meiotic nuclear divisions but not for the initiation of meiosis. Our study defines the roles of autophagy and the proteasome in meiosis: Autophagy mainly affects the initiation of meiosis, whereas the proteasome mainly affects the 2 successive meiotic divisions.Entities:
Keywords: autophagy; meiosis; proteasome; quantitative proteomics; yeast
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Year: 2016 PMID: 27050457 PMCID: PMC4835973 DOI: 10.1080/15548627.2016.1149659
Source DB: PubMed Journal: Autophagy ISSN: 1554-8627 Impact factor: 16.016