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将额外的端粒外DNA序列导入酿酒酵母会导致端粒延长。

Introduction of extra telomeric DNA sequences into Saccharomyces cerevisiae results in telomere elongation.

作者信息

Runge K W, Zakian V A

机构信息

Fred Hutchinson Cancer Research Center, Seattle, Washington 98104.

出版信息

Mol Cell Biol. 1989 Apr;9(4):1488-97. doi: 10.1128/mcb.9.4.1488-1497.1989.

Abstract

The termini of Saccharomyces cerevisiae chromosomes consist of tracts of C1-3A (one to three cytosine and one adenine residue) sequences of approximately 450 base pairs in length. To gain insights into trans-acting factors at telomeres, high-copy-number linear and circular plasmids containing tracts of C1-3A sequences were introduced into S. cerevisiae. We devised a novel system to distinguish by color colonies that maintained the vector at 1 to 5, 20 to 50, and 100 to 400 copies per cell and used it to change the amount of telomeric DNA sequences per cell. An increase in the number of C1-3A sequences caused an increase in the length of telomeric C1-3A repeats that was proportional to plasmid copy number. Our data suggest that telomere growth is inhibited by a limiting factor(s) that specifically recognizes C1-3A sequences and that this factor can be effectively competed for by long tracts of C1-3A sequences at telomeres or on circular plasmids. Telomeres without this factor are exposed to processes that serve to lengthen chromosome ends.

摘要

酿酒酵母染色体的末端由长度约为450个碱基对的C1-3A(一到三个胞嘧啶和一个腺嘌呤残基)序列片段组成。为了深入了解端粒处的反式作用因子,将含有C1-3A序列片段的高拷贝数线性和环状质粒导入酿酒酵母。我们设计了一种新颖的系统,通过颜色区分每个细胞中维持载体数量为1至5、20至50和100至400拷贝的菌落,并利用该系统改变每个细胞中端粒DNA序列的数量。C1-3A序列数量的增加导致端粒C1-3A重复序列的长度增加,且与质粒拷贝数成正比。我们的数据表明,端粒生长受到一种特异性识别C1-3A序列的限制因子的抑制,并且端粒或环状质粒上的长片段C1-3A序列能够有效竞争该因子。没有这种因子的端粒会受到促使染色体末端延长的过程的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06f9/362565/ef4ad8a6bb55/molcellb00052-0120-a.jpg

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