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酿酒酵母的正向氮调节基因GLN3的序列与表达,该基因编码一种具有推定锌指DNA结合结构域的蛋白质。

Sequence and expression of GLN3, a positive nitrogen regulatory gene of Saccharomyces cerevisiae encoding a protein with a putative zinc finger DNA-binding domain.

作者信息

Minehart P L, Magasanik B

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

Mol Cell Biol. 1991 Dec;11(12):6216-28. doi: 10.1128/mcb.11.12.6216-6228.1991.

Abstract

The GLN3 gene of Saccharomyces cerevisiae is required for the activation of transcription of a number of genes in response to the replacement of glutamine by glutamate as source of nitrogen. We cloned the GLN3 gene and constructed null alleles by gene disruption. GLN3 is not essential for growth, but increased copies of GLN3 lead to a drastic decrease in growth rate. The complete nucleotide sequence of the GLN3 gene was determined, revealing one open reading frame encoding a polypeptide of 730 amino acids, with a molecular weight of approximately 80,000. The GLN3 protein contains a single putative Cys2/Cys2 zinc finger which has homology to the Neurospora crassa NIT2 protein, the Aspergillus nidulans AREA protein, and the erythroid-specific transcription factor GATA-1. Immunoprecipitation experiments indicated that the GLN3 protein binds the nitrogen upstream activation sequence of GLN1, the gene encoding glutamine synthetase. Neither control of transcription nor control of initiation of translation of GLN3 is important for regulation in response to glutamine availability.

摘要

酿酒酵母的GLN3基因是激活许多基因转录所必需的,这些基因可响应谷氨酸替代谷氨酰胺作为氮源的情况。我们克隆了GLN3基因并通过基因破坏构建了无效等位基因。GLN3对生长不是必需的,但GLN3基因的额外拷贝会导致生长速率急剧下降。我们测定了GLN3基因的完整核苷酸序列,发现一个开放阅读框编码一个730个氨基酸的多肽,分子量约为80,000。GLN3蛋白包含一个单一的假定Cys2/Cys2锌指结构,它与粗糙脉孢菌的NIT2蛋白、构巢曲霉的AREA蛋白以及红细胞特异性转录因子GATA-1具有同源性。免疫沉淀实验表明,GLN3蛋白结合GLN1(编码谷氨酰胺合成酶的基因)的氮上游激活序列。GLN3的转录控制和翻译起始控制对于响应谷氨酰胺可用性的调节都不重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fd3/361808/543bbc21ca50/molcellb00036-0433-a.jpg

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