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远距离上游调控序列控制粗糙脉孢菌am(GDH)基因座的表达水平。

Distant upstream regulatory sequences control the level of expression of the am (GDH) locus of Neurospora crassa.

作者信息

Frederick G D, Kinsey J A

机构信息

Department of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical School, Kansas City 66103.

出版信息

Curr Genet. 1990 Jul;18(1):53-8. doi: 10.1007/BF00321115.

Abstract

We have constructed deletions in the 5' noncoding sequences of the cloned Neurospora crassa am gene. Vectors with a truncated fragment of the am gene were used in transformation experiments to introduce the deletions into the chromosome by homologous recombination. Analysis of glutamate dehydrogenase (GDH) expression by enzyme assay and immunoblots, as well as Northern and dot blots of poly (A)+ RNA, in the deletion strains indicates that there are two upstream regulatory sequences that control the level of gene expression. The closer of these two elements (URSam alpha) is at approximately 1.4 kb upstream of the transcriptional start site. The second elements (URSam beta) is located between 2.1 and 3.2 kb upstream of the transcription start site. Deletion of either of these two elements reduces am expression to about 50% of the wild-type level. Deletion of both elements reduce am expression to from 5-16% of the wild-type level. Deletion of 1.1 kb of sequence just downstream of URSam alpha, which brings this element to within 300 bp of the transcription start site, had no effect on am expression. Likewise, deletion of 3.5 kb of sequence upstream of URSam beta had no effect on expression. None of these deletions had any effect on the expression of usg-1, a gene of unknown function that is transcribed in the same direction as the am gene, and which terminates about 3.5 kb upstream of the URSam beta element.

摘要

我们构建了克隆的粗糙脉孢菌am基因5'非编码序列的缺失突变体。携带am基因截短片段的载体用于转化实验,通过同源重组将缺失突变引入染色体。对缺失突变菌株中谷氨酸脱氢酶(GDH)表达进行酶活性测定和免疫印迹分析,以及对聚腺苷酸加尾RNA进行Northern印迹和斑点印迹分析,结果表明存在两个上游调控序列控制基因表达水平。这两个元件中较靠近转录起始位点的(URSamα)位于转录起始位点上游约1.4 kb处。第二个元件(URSamβ)位于转录起始位点上游2.1至3.2 kb之间。缺失这两个元件中的任何一个都会使am基因的表达降低至野生型水平的约50%。同时缺失这两个元件会使am基因的表达降低至野生型水平的5%至16%。在URSamα元件下游缺失1.1 kb的序列,使该元件与转录起始位点的距离缩短至300 bp以内,对am基因表达没有影响。同样,在URSamβ元件上游缺失3.5 kb的序列对表达也没有影响。这些缺失突变对usg - 1基因的表达均无影响,usg - 1是一个功能未知的基因,其转录方向与am基因相同,且在URSamβ元件上游约3.5 kb处终止。

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