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粗糙脉孢菌cys-3调控基因的分子克隆与特性分析。

Molecular cloning and characterization of the cys-3 regulatory gene of Neurospora crassa.

作者信息

Paietta J V, Akins R A, Lambowitz A M, Marzluf G A

出版信息

Mol Cell Biol. 1987 Jul;7(7):2506-11. doi: 10.1128/mcb.7.7.2506-2511.1987.

Abstract

The regulatory gene cys-3+ controls the synthesis of a number of enzymes involved in sulfur metabolism. cys-3 mutants show a multiple loss of enzymes in different pathways of sulfur metabolism. The cys-3+ gene was isolated by transformation of an aro-9 qa-2 cys-3 inl strain with a clone bank followed by screening with the "sib selection" method. The library used (pRAL1) contained inserts of Sau3a partial digest fragments of about 9 kilobases as well as the Neurospora qa-2+ gene. Double selection for qa-2+ and cys-3+ function was carried out. The transformants obtained with the isolated cys-3+ clone show recovery of the enzyme activities associated with the cys-3 mutation (e.g., arylsulfatase and sulfate permease). Restriction fragment length polymorphism experiments confirmed the identity of the clone, mRNA studies with Northern blots show that the expression of the cys-3+ gene is inducible. In contrast to cys-3+, the cys-3 (P22) mutant gene was not expressed at a higher level under sulfur-derepressed conditions.

摘要

调控基因cys-3+控制着多种参与硫代谢的酶的合成。cys-3突变体在硫代谢的不同途径中表现出多种酶的缺失。通过用克隆文库转化aro-9 qa-2 cys-3 inl菌株,然后用“同胞选择”方法进行筛选,分离出了cys-3+基因。所使用的文库(pRAL1)包含约9千碱基的Sau3a部分消化片段的插入片段以及粗糙脉孢菌qa-2+基因。对qa-2+和cys-3+功能进行了双重选择。用分离出的cys-3+克隆获得的转化体显示出与cys-3突变相关的酶活性的恢复(例如,芳基硫酸酯酶和硫酸盐通透酶)。限制性片段长度多态性实验证实了该克隆的身份,用Northern印迹进行的mRNA研究表明cys-3+基因的表达是可诱导的。与cys-3+相反,cys-3(P22)突变基因在硫去阻遏条件下没有更高水平的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0abb/365384/115647005291/molcellb00079-0218-a.jpg

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