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对α-鹅膏蕈碱敏感性降低20000倍的突变型秀丽隐杆线虫RNA聚合酶II。

Mutant Caenorhabditis elegans RNA polymerase II with a 20,000-fold reduced sensitivity to alpha-amanitin.

作者信息

Rogalski T M, Golomb M, Riddle D L

机构信息

Division of Biological Sciences, University of Missouri, Columbia 65211.

出版信息

Genetics. 1990 Dec;126(4):889-98. doi: 10.1093/genetics/126.4.889.

Abstract

A doubly mutant ama-1(m118m526) gene results in an RNA polymerase (Rpo) II that is unusually resistant to alpha-amanitin. Rpo II activity in isolated Caenorhabditis elegans cell nuclei is inhibited 50% by alpha-amanitin at a concentration of 150 micrograms/ml, making this enzyme 150 times more resistant to the toxin than Rpo II from the singly mutant allele, ama-1(m118), 20,000 times more resistant than the wild-type Rpo II, and about six times more resistant to amanitin than is Rpo III. It was determined that the SL1 spliced leader precursor is transcribed by Rpo II, and this transcript was used to measure Rpo II activity. The Rpo II activity is unstable in vitro, and the mutant strain has a temperature-sensitive sterile phenotype. The highly resistant double mutant was selected among four million progeny of the mutagenized ama-1(m118) parent by its ability to grow and reproduce in 200 micrograms/ml amanitin in the presence of a permeabilizing agent, Triton X-100.

摘要

双突变ama-1(m118m526)基因会导致RNA聚合酶(Rpo)II对α-鹅膏蕈碱具有异常的抗性。在分离的秀丽隐杆线虫细胞核中,α-鹅膏蕈碱在浓度为150微克/毫升时会抑制50%的Rpo II活性,这使得这种酶对毒素的抗性比单突变等位基因ama-1(m118)的Rpo II高150倍,比野生型Rpo II高20000倍,对鹅膏蕈碱的抗性比Rpo III高约6倍。已确定SL1剪接前导序列前体由Rpo II转录,并且该转录本用于测量Rpo II活性。Rpo II活性在体外不稳定,并且该突变菌株具有温度敏感的不育表型。通过在通透剂Triton X-100存在的情况下,在200微克/毫升鹅膏蕈碱中生长和繁殖的能力,从诱变的ama-1(m118)亲本的四百万后代中筛选出了高度抗性的双突变体。

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