Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1995 Aug;140(4):1235-45.
doi: 10.1093/genetics/140.4.1235.

The role of cdc2 and other genes in meiosis in Schizosaccharomyces pombe

Affiliations

The role of cdc2 and other genes in meiosis in Schizosaccharomyces pombe

Y Iino et al. Genetics. 1995 Aug.

Abstract

The requirement of the cdc2, cdc13 and cdc25 genes for meiosis in Schizosaccharomyces pombe was investigated using three different conditions to induce meiosis. These genes were known to be required for meiosis II. cdc13 and cdc25 are essential for meiosis I. The cdc2 gene, which is required for the initiation of both mitotic S-phase and M-phase, is essential for premeiotic DNA synthesis and meiosis II. The requirement of cdc2 for meiosis I was unclear. This contrasts with Saccharomyces cerevisiae, where CDC28, the homolog of cdc2, is required for meiosis I but not for premeiotic DNA synthesis. Expression of cdc13 and cdc25 was induced after premeiotic DNA synthesis, reaching a sharp peak before the first nuclear division. Expression of cdc22, encoding the large subunit of ribonucleotide reductase, was also induced but the peak was before premeiotic DNA synthesis. The induction of cdc13 and cdc25 was largely dependent on DNA synthesis and the function of the mei4 gene. The mei4 gene itself was also induced in a DNA synthesis-dependent manner. The chain of gene expression activating cdc25 may be important as part of the mechanism that ensures the dependency of nuclear division on DNA replication during meiosis.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Cell. 1990 Feb 23;60(4):665-73 - PubMed
    1. Cell. 1991 Oct 4;67(1):189-96 - PubMed
    1. Cell. 1994 Aug 12;78(3):487-98 - PubMed
    1. Cell. 1990 May 4;61(3):375-8 - PubMed
    1. Proc Natl Acad Sci U S A. 1980 Sep;77(9):5201-5 - PubMed

Publication types

MeSH terms