Larson T G, Nuss D L
Molecular Oncology and Virology, Roche Institute of Molecular Biology, Roche Research Center, Nutley, NJ 07110.
Proc Natl Acad Sci U S A. 1993 Jan 1;90(1):148-52. doi: 10.1073/pnas.90.1.148.
Exposure to cyclosporin A (CspA) increased laccase (lac-1) transcript accumulation in the chestnut blight fungus Cryphonectria parasitica. This response was suppressed by compounds that interfere with calcium-dependent signal transduction and by the presence of a virulence-attenuating mycovirus. CspA stimulated the accumulation of mRNA from a nonhomologous reporter fused to the lac-1 promoter, indicating that the increased transcript levels resulted from an increase in promoter activity. Based on the current model for the regulation of lac-1 transcription, these results suggest that CspA interferes with a negative regulatory pathway that normally constrains lac-1 promoter activity. Significantly, CspA did not stimulate lac-1 transcription in mutant strains deficient in CspA binding activity, directly demonstrating a requirement for the interaction of CspA and cyclophilin in the modulation of lac-1 transcription. Our results establish that CspA treatment can stimulate gene transcription and that cyclophilin is the cellular receptor that mediates this activity.
暴露于环孢菌素A(CspA)会增加栗疫病菌(Cryphonectria parasitica)中漆酶(lac-1)转录本的积累。干扰钙依赖性信号转导的化合物以及一种减毒致病的真菌病毒的存在会抑制这种反应。CspA刺激了与lac-1启动子融合的非同源报告基因的mRNA积累,表明转录水平的增加是由启动子活性增强所致。基于当前对lac-1转录调控的模型,这些结果表明CspA干扰了通常限制lac-1启动子活性的负调控途径。值得注意的是,CspA在缺乏CspA结合活性的突变菌株中不会刺激lac-1转录,直接证明了CspA与亲环蛋白相互作用对调节lac-1转录的必要性。我们的结果表明,CspA处理可以刺激基因转录,并且亲环蛋白是介导这种活性的细胞受体。