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酿酒酵母中天冬酰胺合成酶编码基因ASN1和ASN2的克隆:CCAAT盒结合因子的差异调控

Cloning of the ASN1 and ASN2 genes encoding asparagine synthetases in Saccharomyces cerevisiae: differential regulation by the CCAAT-box-binding factor.

作者信息

Dang V D, Valens M, Bolotin-Fukuhara M, Daignan-Fornier B

机构信息

Láboratoire de Génétique Moléculaire, Institut de Génétique et Microbiologie, Orsay, France.

出版信息

Mol Microbiol. 1996 Nov;22(4):681-92. doi: 10.1046/j.1365-2958.1996.d01-1715.x.

Abstract

Two new yeast genes, named ASN1 and ASN2, were isolated by complementation of the growth defect of an asparagine auxotrophic mutant. Genetical analysis indicates that these two genes are allelic to the asnA and asnB loci described previously. Simultaneous disruption of both genes leads to a total asparagine auxotrophy, while disruption of asn1 or asn2 alone has no effect on growth under tested conditions. Nucleotide sequences of ASN1 and ASN2 revealed striking similarities with genes encoding asparagine synthetase (AS) from other organisms. Regulation of ASN1 and ASN2 expression was studied using lacZ fusions and both genes were found to be several times less expressed in the absence of the transcription activator Gcn4p. The HAP complex, another transcription factor that binds to CCAAT-box sequences, was shown to specifically affect ASN1 expression. Hap2p and Hap3p subunits of the HAP complex are required for optimal expression of ASN1, while the Hap4p regulatory subunit, which is required for regulation by the carbon source, plays a minor role in this process. Consistent with the weak effect of Hap4p, the carbon source does not significantly affect expression of ASN1. Our results show that the role of the HAP complex is not limited to activation of genes required for respiratory metabolism.

摘要

通过对天冬酰胺营养缺陷型突变体生长缺陷的互补作用,分离出了两个新的酵母基因,命名为ASN1和ASN2。遗传学分析表明,这两个基因与先前描述的asnA和asn B位点等位。同时破坏这两个基因会导致完全的天冬酰胺营养缺陷,而单独破坏asn1或asn2在测试条件下对生长没有影响。ASN1和ASN2的核苷酸序列与来自其他生物体的编码天冬酰胺合成酶(AS)的基因有显著相似性。使用lacZ融合研究了ASN1和ASN2的表达调控,发现这两个基因在没有转录激活因子Gcn4p的情况下表达量降低了几倍。HAP复合体是另一种与CCAAT框序列结合的转录因子,已证明它能特异性影响ASN1的表达。HAP复合体的Hap2p和Hap3p亚基是ASN1最佳表达所必需的,而碳源调控所需的Hap4p调节亚基在此过程中起次要作用。与Hap4p的微弱作用一致,碳源对ASN1的表达没有显著影响。我们的结果表明,HAP复合体的作用不仅限于激活呼吸代谢所需的基因。

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