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粗糙脉孢菌芳基硫酸酯酶结构基因的分子克隆及调控分析

Molecular cloning and regulatory analysis of the arylsulfatase structural gene of Neurospora crassa.

作者信息

Paietta J V

机构信息

Department of Biochemistry, Wright State University, Dayton, Ohio 45435.

出版信息

Mol Cell Biol. 1989 Sep;9(9):3630-7. doi: 10.1128/mcb.9.9.3630-3637.1989.

Abstract

The ars-1+ gene of Neurospora crassa encodes the enzyme arylsulfatase. ars-1+ is in a group of highly regulated sulfur-related structural genes that are expressed under conditions of sulfur limitation and are under coordinate control of the cys-3+ and scon+ regulatory genes. The ars-1+ gene was cloned by chromosome walking from the qa gene cluster, using a lambda library. Cotransformation of an N. crassa ars-1 mutant with the isolated lambda clones and the benomyl resistance gene, followed by assay for arylsulfatase activity, was used to screen for the ars-1+ gene. Further confirmation that the cloned segment mapped to the ars-1+ locus was obtained by restriction-fragment-length polymorphism analysis. Northern (RNA) blot analysis showed that the ars-1+ gene was transcribed to give an mRNA of 2.3 kilobases. In wild-type cells, the ars-1+ transcript was abundant under sulfur-derepressing conditions but absent under repressing conditions. Time course analysis showed that the appearance of ars-1+ message in sulfur-derepressed cultures paralleled the appearance of arylsulfatase enzyme activity. In addition, transcription of ars-1+ was detected only under derepressing conditions in a nuclear transcription assay. In a cys-3 regulatory mutant that was unable to synthesize arylsulfatase (or other sulfur-controlled enzymes), there was no ars-1+ transcript under repressing or derepressing conditions. In a temperature-sensitive cys-3 mutant, the ars-1+ transcript was present only at the permissive growth temperature and under sulfur derepression. A negative regulatory mutant, sconc, displayed both constitutive expression of arylsulfatase enzyme activity and content of ars-1+ message.

摘要

粗糙脉孢菌的ars-1+基因编码芳基硫酸酯酶。ars-1+属于一组高度受调控的与硫相关的结构基因,这些基因在硫限制条件下表达,并受cys-3+和scon+调控基因的协同控制。利用λ文库通过染色体步移从qa基因簇克隆了ars-1+基因。用分离的λ克隆和苯菌灵抗性基因对粗糙脉孢菌ars-1突变体进行共转化,随后检测芳基硫酸酯酶活性,以此筛选ars-1+基因。通过限制性片段长度多态性分析进一步证实克隆片段定位于ars-1+位点。Northern(RNA)印迹分析表明,ars-1+基因转录产生一条2.3千碱基的mRNA。在野生型细胞中,ars-1+转录本在硫去阻遏条件下丰富,但在阻遏条件下不存在。时间进程分析表明,硫去阻遏培养物中ars-1+信息的出现与芳基硫酸酯酶活性的出现平行。此外,在核转录试验中,仅在去阻遏条件下检测到ars-1+的转录。在一个无法合成芳基硫酸酯酶(或其他硫控制酶)的cys-3调控突变体中,在阻遏或去阻遏条件下均无ars-1+转录本。在一个温度敏感的cys-3突变体中,ars-1+转录本仅在允许生长温度和硫去阻遏条件下存在。一个负调控突变体sconc,显示出芳基硫酸酯酶活性和ars-1+信息含量的组成型表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f0/362423/4a2219a0f190/molcellb00057-0053-a.jpg

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