Gregan Juraj, Rabitsch Peter K, Sakem Benjamin, Csutak Ortansa, Latypov Vitaly, Lehmann Elisabeth, Kohli Juerg, Nasmyth Kim
Research Institute of Molecular Pathology, Dr. Bohr-Gasse 7, A-1030 Vienna, Austria.
Curr Biol. 2005 Sep 20;15(18):1663-9. doi: 10.1016/j.cub.2005.07.059.
Two rounds of chromosome segregation after only a single round of DNA replication enable the production of haploid gametes from diploid precursors during meiosis. To identify genes involved in meiotic chromosome segregation, we developed an efficient strategy to knock out genes in the fission yeast on a large scale. We used this technique to delete 180 functionally uncharacterized genes whose expression is upregulated during meiosis. Deletion of two genes, sgo1 and mde2, caused massive chromosome missegregation. sgo1 is required for retention of centromeric sister-chromatid cohesion after anaphase I. We show here that mde2 is required for formation of the double-strand breaks necessary for meiotic recombination.
在减数分裂过程中,仅一轮DNA复制后进行两轮染色体分离,就能使二倍体前体产生单倍体配子。为了鉴定参与减数分裂染色体分离的基因,我们开发了一种在裂殖酵母中大规模敲除基因的有效策略。我们利用这项技术删除了180个功能未明确的基因,这些基因在减数分裂过程中表达上调。删除sgo1和mde2这两个基因会导致大量染色体错分离。sgo1是后期I后着丝粒姐妹染色单体黏连保留所必需的。我们在此表明,mde2是减数分裂重组所需双链断裂形成所必需的。