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NDT80,酿酒酵母中从粗线期退出所需的一个减数分裂特异性基因。

NDT80, a meiosis-specific gene required for exit from pachytene in Saccharomyces cerevisiae.

作者信息

Xu L, Ajimura M, Padmore R, Klein C, Kleckner N

机构信息

Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA.

出版信息

Mol Cell Biol. 1995 Dec;15(12):6572-81. doi: 10.1128/MCB.15.12.6572.

Abstract

We describe the identification of a new meiosis-specific gene of Saccharomyces cerevisiae, NDT80. The ndt80 null and point mutants arrest at the pachytene stage of meiosis, with homologs connected by full-length synaptonemal complexes and spindle pole bodies duplicated but unseparated. Meiotic recombination in an ndt80 delta mutant is relatively normal, although commitment to heteroallelic recombination is elevated two- to threefold and crossing over is decreased twofold compared with those of the wild type. ndt80 arrest is not alleviated by mutations in early recombination genes, e.g., SPO11 or RAD50, and thus cannot be attributed to an intermediate block in prophase chromosome metabolism like that observed in several other mutants. The ndt80 mutant phenotype during meiosis most closely resembles that of a cdc28 mutant, which contains a thermolabile p34, the catalytic subunit of maturation-promoting factor. Cloning and molecular analysis reveal that the NDT80 gene maps on the right arm of chromosome VIII between EPT1 and a Phe-tRNA gene, encodes a 627-amino-acid protein which exhibits no significant homology to other known proteins, and is transcribed specifically during middle meiotic prophase. The NDT80 gene product could be a component of the cell cycle regulatory machinery involved in the transition out of pachytene, a participant in an unknown aspect of meiosis sensed by a pachytene checkpoint, or a SPO11- and RAD50-independent component of meiotic chromosomes that is the target of cell cycle signaling.

摘要

我们描述了酿酒酵母中一个新的减数分裂特异性基因NDT80的鉴定。ndt80缺失突变体和点突变体在减数分裂的粗线期停滞,同源染色体由全长联会复合体连接,纺锤体极体已复制但未分离。与野生型相比,ndt80Δ突变体中的减数分裂重组相对正常,尽管杂合等位基因重组的发生率提高了两到三倍,交叉发生率降低了两倍。早期重组基因(如SPO11或RAD50)的突变并不能缓解ndt80的停滞,因此不能将其归因于前期染色体代谢中的中间阻滞,就像在其他几个突变体中观察到的那样。减数分裂期间ndt80突变体的表型与cdc28突变体最为相似,后者含有热不稳定的p34,即成熟促进因子的催化亚基。克隆和分子分析表明,NDT80基因定位于第八条染色体右臂上EPT1和一个苯丙氨酸tRNA基因之间,编码一个627个氨基酸的蛋白质,该蛋白质与其他已知蛋白质没有明显的同源性,并且在减数分裂前期中期特异性转录。NDT80基因产物可能是参与从粗线期过渡的细胞周期调控机制的一个组成部分,是粗线期检查点所感知的减数分裂未知方面的参与者,或者是减数分裂染色体中不依赖SPO11和RAD50的组成部分,是细胞周期信号传导的靶点。

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