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酿酒酵母1号染色体DNA的分子克隆:CDC24基因及该染色体相邻区域的分离与特性分析

Molecular cloning of chromosome I DNA from Saccharomyces cerevisiae: isolation and characterization of the CDC24 gene and adjacent regions of the chromosome.

作者信息

Coleman K G, Steensma H Y, Kaback D B, Pringle J R

出版信息

Mol Cell Biol. 1986 Dec;6(12):4516-25. doi: 10.1128/mcb.6.12.4516-4525.1986.

Abstract

Molecular cloning techniques were used to isolate and characterize the DNA including and surrounding the CDC24 and PYK1 genes on the left arm of chromosome I of the yeast Saccharomyces cerevisiae. A plasmid that complemented a temperature-sensitive cdc24 mutation was isolated from a yeast genomic DNA library in a shuttle vector. Plasmids containing pyk1-complementing DNA were obtained from other investigators. Several lines of evidence (including one-step gene replacement experiments) demonstrated that the complementing plasmids contained the bona fide CDC24 and PYK1 genes. These sequences were then used to isolate additional DNA from chromosome I by probing a yeast genomic DNA library in a lambda vector. A total of 28 kilobases (kb) of contiguous DNA surrounding the CDC24 and PYK1 genes was isolated, and a restriction map was determined. Electron microscopy of R-loop-containing DNA and RNA blot hybridization analyses indicated that an 18-kb segment contained at least seven transcribed regions, only three of which corresponded to previously known genes (CDC24, PYK1, and CYC3). Southern blot hybridization experiments suggested that none of the genes in this region was duplicated elsewhere in the yeast genome. The centers of CDC24 and PYK1 were only approximately 7.5 kb apart, although the genetic map distance between them is approximately 13 centimorgans. As previous studies with S. cerevisiae have indicated that 1 centimorgan generally corresponds to approximately 3 kb, the region between CDC24 and PYK1 appears to undergo meiotic recombination at an unusually high frequency.

摘要

利用分子克隆技术分离并鉴定了酿酒酵母1号染色体左臂上包含CDC24和PYK1基因及其周围的DNA。从穿梭载体中的酵母基因组DNA文库中分离出了一个能互补温度敏感型cdc24突变的质粒。含有pyk1互补DNA的质粒由其他研究人员提供。几条证据线(包括一步基因置换实验)表明,互补质粒包含真正的CDC24和PYK1基因。然后利用这些序列通过探测λ载体中的酵母基因组DNA文库从1号染色体中分离出更多的DNA。总共分离出了围绕CDC24和PYK1基因的28千碱基(kb)连续DNA,并确定了限制酶切图谱。含R环的DNA的电子显微镜观察和RNA印迹杂交分析表明,一个18 kb的片段包含至少七个转录区域,其中只有三个对应于先前已知的基因(CDC24、PYK1和CYC3)。Southern印迹杂交实验表明,该区域的基因在酵母基因组的其他地方均未重复。CDC24和PYK1的中心相距仅约7.5 kb,尽管它们之间的遗传图谱距离约为13厘摩。正如先前对酿酒酵母的研究表明,1厘摩通常对应约3 kb,CDC24和PYK1之间的区域似乎以异常高的频率发生减数分裂重组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3465/367236/00fb97a3b50e/molcellb00096-0384-a.jpg

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