A Meiosis-Specific Cyclin Regulated by Splicing Is Required for Proper Progression through Meiosis

Author:

Malapeira Jordi1,Moldón Alberto1,Hidalgo Elena1,Smith Gerald R.2,Nurse Paul3,Ayté José1

Affiliation:

1. Cell Signaling Unit, Universitat Pompeu Fabra, Barcelona, Spain

2. Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109

3. The Rockefeller University, New York, New York 10021

Abstract

ABSTRACT The meiotic cell cycle is modified from the mitotic cell cycle by having a premeiotic S phase which leads to high levels of recombination, a reductional pattern of chromosome segregation at the first division, and a second division with no intervening DNA synthesis. Cyclin-dependent kinases are essential for progression through the meiotic cell cycle, as for the mitotic cycle. Here we show that a fission yeast cyclin, Rem1, is present only during meiosis. Cells lacking Rem1 have impaired meiotic recombination, and Rem1 is required for premeiotic DNA synthesis when Cig2 is not present. rem1 expression is regulated at the level of both transcription and splicing, with Mei4 as a positive and Cig2 a negative factor of rem1 splicing. This regulation ensures the timely appearance of the different cyclins during meiosis, which is required for the proper progression through the meiotic cell cycle. We propose that the meiosis-specific B-type cyclin Rem1 has a central role in bringing about progression through meiosis.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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