Regulatory mechanisms in meiosis
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IME4, a Gene That Mediates MAT and Nutritional Control of Meiosis in Saccharomyces cerevisiae
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Role of IME1 Expression in Regulation of Meiosis in Saccharomyces cerevisiae
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Nutritional Regulation of Meiosis-Specific Gene Expression in Saccharomyces cerevisiae
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Identification of Functionally Related Genes That Stimulate Early Meiotic Gene Expression in Yeast
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Meiotic Induction of the Yeast HOP1 Gene is Controlled by Positive and Negative Regulatory Sites
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The Yeast UME6 Gene Product is Required for Transcriptional Repression Medicated by the CAR1 URS1 Repressor Binding Site
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RPD1 (SIN3/UME4) is Required for Maximal Activation and Repression of Diverse Yeast Genes
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Positive Control of Sporulation-Specific Genes by the IME1 and IME2 Products in Saccharomyces cerevisiae
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Early Meiotic Transcripts are Highly Unstable in Saccharomyces cerevisiae
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S.pombe pac1+, Whose Overexpression Inhibits Sexual Development, Encodes a Ribonuclease III-Like RNase
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Meiosis-Specific RNA Splicing in Yeast
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DMC1: A Meiosis-Specific Yeast Homolog of E. coli recA Required for Recombination, Synaptonemal Complex Formation, and Cell Cycle Progression
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Cited by (30)
Control of Meiosis by Respiration
2008, Current BiologyCitation Excerpt :We next tested whether induction of the early meiotic genes allowed sporulation in KCl by utilizing a strain bearing an allele of the protein kinase Ime2, ime2-as, which can be reversibly inhibited by the ATP analog 1-NA-PP1 [2]. In the presence of the inhibitor, IME1, a transcription factor governing entry into meiosis [3], and other early meiotic genes are expressed but premeiotic DNA replication and subsequent meiotic events are not initiated [2] (compare also Figures S1A and S3A). When the inhibitor was washed out of KAc cultures, cells sporulated efficiently only when released into KAc, whereas tetranucleate formation was decreased by more than 7-fold in cells released into KCl medium (Figure 1B).
Ume1p Represses Meiotic Gene Transcription in Saccharomyces cerevisiae through Interaction with the Histone Deacetylase Rpd3p
2003, Journal of Biological ChemistryDifferential regulation of growth and checkpoint control mediated by a Cdc25 mitotic phosphatase from Pneumocystis carinii
2001, Journal of Biological ChemistryCitation Excerpt :In response to environmental stimuli, signal transduction pathways are activated that eventually impact on the cell cycle machinery. Cdc25 is a key regulator of several cellular processes including regulating entry into mitosis, meiotic phase transitions, and maintaining G2/M and S/M checkpoints in the response to DNA damage and incomplete DNA replication (26-31). The protein complexes that sense DNA damage or stalled DNA replication forks transmit signals that ultimately lead to the inactivation of Cdc2 (32, 33, 37).
Stopping and starting the meiotic cell cycle
1997, Current Opinion in Genetics and DevelopmentMaternal Xenopus Cdk2-cyclin E complexes function during meiotic and early embryonic cell cycles that lack a G<inf>1</inf> phase
1995, Journal of Biological Chemistry