Young Jennifer A, Hyppa Randy W, Smith Gerald R
Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Genetics. 2004 Jun;167(2):593-605. doi: 10.1534/genetics.103.023762.
During meiosis DNA double-strand breaks initiate recombination in the distantly related budding and fission yeasts and perhaps in most eukaryotes. Repair of broken meiotic DNA is essential for formation of viable gametes. We report here distinct but overlapping sets of proteins in these yeasts required for formation and repair of double-strand breaks. Meiotic DNA breakage in Schizosaccharomyces pombe did not require Rad50 or Rad32, although the homologs Rad50 and Mre11 are required in Saccharomyces cerevisiae; these proteins are required for meiotic DNA break repair in both yeasts. DNA breakage required the S. pombe midmeiosis transcription factor Mei4, but the structurally unrelated midmeiosis transcription factor Ndt80 is not required for breakage in S. cerevisiae. Rhp51, Swi5, and Rad22 + Rti1 were required for full levels of DNA repair in S. pombe, as are the related S. cerevisiae proteins Rad51, Sae3, and Rad52. Dmc1 was not required for repair in S. pombe, but its homolog Dmc1 is required in the well-studied strain SK1 of S. cerevisiae. Additional proteins required in one yeast have no obvious homologs in the other yeast. The occurrence of conserved and nonconserved proteins indicates potential diversity in the mechanism of meiotic recombination and divergence of the machinery during the evolution of eukaryotes.
在减数分裂过程中,DNA双链断裂引发了远缘相关的芽殖酵母和裂殖酵母中的重组,可能在大多数真核生物中也是如此。断裂的减数分裂DNA的修复对于形成有活力的配子至关重要。我们在此报告这些酵母中双链断裂的形成和修复所需的不同但重叠的蛋白质组。粟酒裂殖酵母中的减数分裂DNA断裂不需要Rad50或Rad32,尽管酿酒酵母中需要同源物Rad50和Mre11;这两种蛋白质在两种酵母中都是减数分裂DNA断裂修复所必需的。DNA断裂需要粟酒裂殖酵母减数分裂中期转录因子Mei4,但结构上不相关的减数分裂中期转录因子Ndt80在酿酒酵母的断裂过程中不是必需的。Rhp51、Swi5和Rad22 + Rti1是粟酒裂殖酵母中DNA完全修复水平所必需的,酿酒酵母中相关蛋白质Rad51、Sae3和Rad52也是如此。Dmc1在粟酒裂殖酵母的修复中不是必需的,但其同源物Dmc1在经过充分研究的酿酒酵母菌株SK1中是必需的。一种酵母中所需的其他蛋白质在另一种酵母中没有明显的同源物。保守和非保守蛋白质的存在表明减数分裂重组机制存在潜在差异,以及在真核生物进化过程中该机制的分歧。