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酵母同工-2-细胞色素c基因中三个转录突变的分子特征分析。

The molecular characterization of three transcriptional mutations in the yeast iso-2-cytochrome c gene.

作者信息

Montgomery D L, Boss J M, McAndrew S J, Marr L, Walthall D A, Zitomer R S

出版信息

J Biol Chem. 1982 Jul 10;257(13):7756-61.

PMID:6282853
Abstract

Three mutations, each of which causes overproduction of iso-2-cytochrome c, were characterized biochemically. Two, CYP3-4 and CYP3-15, were previously shown to be cis-dominant and map to the CYC7 locus which encodes the iso-2 protein, while the third, cyp1-16, maps to an unliked locus. All three mutations caused dramatically increased levels of transcription of the CYC7 gene, and the CYC7 mRNA in mutant cells was found to be the same size as that in wild type cells. The CYP3-4 mutation was found to be caused by the integration of a transposable element, Tyl, 269 base pairs 5' to the coding sequences. The CYP3-15 mutation was also found to alter the DNA, probably through a deletion or inversion with one endpoint 285 base pairs upstream from the coding sequence. The CYC7 gene in both wild type and mutant cells was not subject to catabolite repression.

摘要

对三种均导致异-2-细胞色素c过量产生的突变进行了生化特性分析。其中两种突变,即CYP3-4和CYP3-15,先前已证明是顺式显性的,并且定位于编码异-2蛋白的CYC7基因座,而第三种突变cyp1-16则定位于一个不相关的基因座。所有这三种突变均导致CYC7基因的转录水平显著增加,并且发现突变细胞中的CYC7 mRNA大小与野生型细胞中的相同。发现CYP3-4突变是由一个转座因子Tyl整合到编码序列上游269个碱基对处引起的。还发现CYP3-15突变改变了DNA,可能是通过缺失或倒位,其中一个端点位于编码序列上游285个碱基对处。野生型和突变型细胞中的CYC7基因均不受分解代谢物阻遏作用的影响。

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