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The RNA‐binding protein Spo5 promotes meiosis II by regulating cyclin Cdc13 in fission yeast
Author(s) -
Arata Mayumi,
Sato Masamitsu,
Yamashita Akira,
Yamamoto Masayuki
Publication year - 2014
Publication title -
genes to cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 115
eISSN - 1365-2443
pISSN - 1356-9597
DOI - 10.1111/gtc.12133
Subject(s) - biology , meiosis , schizosaccharomyces pombe , microbiology and biotechnology , meiosis ii , mutant , schizosaccharomyces , cyclin , genetics , cell cycle , gene
Meiosis comprises two consecutive nuclear divisions, meiosis I and II. Despite this unique progression through the cell cycle, little is known about the mechanisms controlling the sequential divisions. In this study, we carried out a genetic screen to identify factors that regulate the initiation of meiosis II in the fission yeast S chizosaccharomyces pombe . We identified mutants deficient in meiosis II progression and repeatedly isolated mutants defective in spo5 , which encodes an RNA‐binding protein. Using fluorescence microscopy to visualize YFP‐tagged protein, we found that spo5 mutant cells precociously lost Cdc13, the major B‐type cyclin in fission yeast, before meiosis II. Importantly, the defect in meiosis II was rescued by increasing CDK activity. In wild‐type cells, cdc13 transcripts increased during meiosis II, but this increase in cdc13 expression was weaker in spo5 mutants. Thus, Spo5 is a novel regulator of meiosis II that controls the level of cdc13 expression and promotes de novo synthesis of Cdc13. We previously reported that inhibition of Cdc13 degradation is necessary to initiate meiosis II; together with the previous information, the current findings indicate that the dual control of Cdc13 by de novo synthesis and suppression of proteolysis ensures the progression of meiosis II.