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酵母着丝粒DNA的功能筛选与分析

Functional selection and analysis of yeast centromeric DNA.

作者信息

Hieter P, Pridmore D, Hegemann J H, Thomas M, Davis R W, Philippsen P

出版信息

Cell. 1985 Oct;42(3):913-21. doi: 10.1016/0092-8674(85)90287-9.

Abstract

A direct selection procedure has been used to isolate 11 distinct yeast genomic DNA fragments that eliminate the extreme segregation bias characteristic of autonomously replicating yeast plasmids. The selection scheme takes advantage of the fact that the cloned ochre suppressing tRNA gene, SUP11, is lethal at high copy number and therefore causes cell death when present on an ARS plasmid that lacks a cis-acting partition function. Each of the cloned DNA sequences was mapped to specific yeast chromosomes by hybridization to chromosome-sized DNA molecules separated by alternating field electrophoresis. Ten of the cloned fragments correspond to chromosomal centromeres; one fragment corresponds to the cis-acting locus required for endogenous 2 mu plasmid stability. Nucleotide sequence comparison of the ten centromere DNAs gives a new picture of conserved centromere DNA elements.

摘要

一种直接筛选程序已被用于分离11个不同的酵母基因组DNA片段,这些片段消除了自主复制酵母质粒特有的极端分离偏差。该筛选方案利用了这样一个事实,即克隆的赭石抑制tRNA基因SUP11在高拷贝数时是致死的,因此当存在于缺乏顺式作用分配功能的ARS质粒上时会导致细胞死亡。通过与交变电场电泳分离的染色体大小的DNA分子杂交,将每个克隆的DNA序列定位到特定的酵母染色体上。其中10个克隆片段对应于染色体着丝粒;一个片段对应于内源性2μm质粒稳定性所需的顺式作用位点。对这10个着丝粒DNA的核苷酸序列比较给出了保守着丝粒DNA元件的新图景。

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