Hollingsworth N M, Byers B
Department of Genetics, University of Washington, Seattle 98195.
Genetics. 1989 Mar;121(3):445-62. doi: 10.1093/genetics/121.3.445.
The recessive mutation, hop1-1, was isolated by use of a screen designed to detect mutations defective in homologous chromosomal pairing during meiosis in Saccharomyces cerevisiae. Mutants in HOP1 displayed decreased levels of meiotic crossing over and intragenic recombination between markers on homologous chromosomes. In contrast, assays of the hop1-1 mutation in a spo13-1 haploid disomic for chromosome III demonstrated that intrachromosomal recombination between directly duplicated sequences was unaffected. The spores produced by SPO13 diploids homozygous for hop1 were largely inviable, as expected for a defect in interhomolog recombination that results in high levels of nondisjunction. HOP1 was cloned by complementation of the spore lethality phenotype and the cloned gene was used to map HOP1 to the LYS11-HIS6 interval on the left arm of chromosome IX. Electron microscopy revealed that diploids homozygous for hop1 fail to form synaptonemal complex, which normally provides the structural basis for homolog pairing. We propose that HOP1 acts in meiosis primarily to promote chromosomal pairing, perhaps by encoding a component of the synaptonemal complex.
隐性突变体hop1-1是通过一种筛选方法分离得到的,该筛选旨在检测酿酒酵母减数分裂过程中同源染色体配对缺陷的突变。HOP1突变体的减数分裂交叉互换水平以及同源染色体上标记之间的基因内重组水平降低。相比之下,在第三条染色体的spo13-1单倍体二体中对hop1-1突变进行检测表明,直接重复序列之间的染色体内重组不受影响。如预期的那样,对于同源重组缺陷导致高水平不分离的情况,hop1纯合的SPO13二倍体产生的孢子大多无法存活。通过对孢子致死表型的互补作用克隆了HOP1,并且利用克隆的基因将HOP1定位到第九条染色体左臂上的LYS11-HIS6区间。电子显微镜显示,hop1纯合的二倍体无法形成联会复合体,而联会复合体通常为同源配对提供结构基础。我们提出,HOP1在减数分裂中主要起促进染色体配对的作用,可能是通过编码联会复合体的一个组分来实现的。