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构巢曲霉metR基因编码一种bZIP蛋白,该蛋白可激活硫代谢基因的转录。

The Aspergillus nidulans metR gene encodes a bZIP protein which activates transcription of sulphur metabolism genes.

作者信息

Natorff Renata, Sieńko Marzena, Brzywczy Jerzy, Paszewski Andrzej

机构信息

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 5A Pawińskiego Str., 02-106 Warszawa, Poland.

出版信息

Mol Microbiol. 2003 Aug;49(4):1081-94. doi: 10.1046/j.1365-2958.2003.03617.x.

Abstract

The identification, isolation and characterization of a new Aspergillus nidulans positive-acting gene metR, which encodes a transcriptional activator of sulphur metabolism, is reported. metR mutants are tight auxotrophs requiring methionine or homocysteine for growth. Mutations in the metR gene are epistatic to mutations in the negative-acting sulphur regulatory scon genes. The metR coding sequence is interrupted by a single intron of 492 bp which is unusually long for fungi. Aspergillus nidulans METR is a member of bZIP family of DNA-binding proteins. The bZIP domains of METR and the Neurospora crassa CYS3 transcriptional activator of sulphur genes are highly similar. Although Neurospora cys-3 gene does not substitute for the metR function, a chimeric metR gene with a cys-3 bZIP domain is able to transform the DeltametR mutant to methionine prototrophy. This indicates that METR recognizes the same regulatory sequence as CYS3. The metR gene is not essential, as deletion mutants are viable and have similar phenotype as point mutants. In contrast to the Neurospora cys-3, transcription of the metR gene was found to be regulated neither by METR protein nor by sulphur source. Transcription of metR gene is derepressed in the sconB2 mutant. Transcription of genes encoding sulphate permease, homocysteine synthase, cysteine synthase, ATP-sulphurylase, and sulphur controller--sconB is strongly regulated by the metR gene product and depends on the character of the metR mutation and sulphur supplementation.

摘要

报道了一种新的构巢曲霉正向作用基因metR的鉴定、分离和特性分析,该基因编码硫代谢的转录激活因子。metR突变体是严格的营养缺陷型,生长需要甲硫氨酸或同型半胱氨酸。metR基因中的突变对负向作用的硫调节基因scon的突变具有上位性。metR编码序列被一个492bp的单一内含子打断,这对真菌来说异常长。构巢曲霉METR是DNA结合蛋白bZIP家族的成员。METR的bZIP结构域与粗糙脉孢菌硫基因的转录激活因子CYS3高度相似。虽然粗糙脉孢菌cys-3基因不能替代metR的功能,但具有cys-3 bZIP结构域的嵌合metR基因能够将DeltametR突变体转化为甲硫氨酸原养型。这表明METR识别与CYS3相同的调控序列。metR基因不是必需的,因为缺失突变体是可行的,并且具有与点突变体相似的表型。与粗糙脉孢菌cys-3不同,发现metR基因的转录既不受METR蛋白调控,也不受硫源调控。metR基因在sconB2突变体中去阻遏。编码硫酸盐通透酶、同型半胱氨酸合酶、半胱氨酸合酶、ATP硫酸化酶和硫调控因子——sconB的基因转录受metR基因产物的强烈调控,并取决于metR突变的性质和硫的补充情况。

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