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酿酒酵母中两个调控方式不同的氮分解代谢基因的诱导表达需要DAL81基因产物。

The DAL81 gene product is required for induced expression of two differently regulated nitrogen catabolic genes in Saccharomyces cerevisiae.

作者信息

Bricmont P A, Daugherty J R, Cooper T G

机构信息

Department of Microbiology and Immunology, University of Tennessee, Memphis 38163.

出版信息

Mol Cell Biol. 1991 Feb;11(2):1161-6. doi: 10.1128/mcb.11.2.1161-1166.1991.

Abstract

We demonstrate that the DAL81 gene, previously thought to be specifically required for induced expression of the allantoin pathway genes in Saccharomyces cerevisiae, functions in a more global manner. The data presented show it to be required for utilization of 4-aminobutyrate as a nitrogen source and for 4-aminobutyrate-induced increases in the steady-state levels of UGA1 mRNA. The DAL81 gene encodes a 970-amino-acid protein containing sequences homologous to the Zn(II)2Cys6 motif and two stretches of polyglutamine residues. Deletion of sequences homologous to the Zn(II)2Cys6 motif did not result in a detectable loss of function. On the other hand, loss of one of the polyglutamine stretches, but not the other, resulted in a 50% loss of DAL81 function.

摘要

我们证明,先前认为在酿酒酵母中对尿囊素途径基因的诱导表达具有特异性需求的DAL81基因,具有更广泛的功能。所呈现的数据表明,它对于将4-氨基丁酸用作氮源以及4-氨基丁酸诱导的UGA1 mRNA稳态水平的增加是必需的。DAL81基因编码一种970个氨基酸的蛋白质,该蛋白质包含与Zn(II)2Cys6基序同源的序列以及两段聚谷氨酰胺残基。与Zn(II)2Cys6基序同源的序列缺失并未导致可检测到的功能丧失。另一方面,其中一段聚谷氨酰胺序列缺失(而非另一段)导致DAL81功能丧失50%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5ad/359801/e824640fd3e4/molcellb00137-0589-a.jpg

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