Case C C, Roels S M, González J E, Simons E L, Simons R W
Department of Microbiology, University of California, Los Angeles 90024.
Gene. 1988 Dec 10;72(1-2):219-36. doi: 10.1016/0378-1119(88)90147-3.
Genetic analysis of eleven mutations affecting the IS10 promoters, pIN and pOUT, involved in anti-sense RNA control of transposase gene expression, and characterization of the transcripts, reveal that: (i) The transposase message (RNA-IN) and the anti-sense RNA (RNA-OUT) have been unambiguously identified in vivo. (ii) Five mutations affect pIN activity, and establish that pIN is the only IS10 promoter transcribing the tnp gene, and the only such IS10 promoter that responds to DNA-adenine methylation. (iii) Six mutations alter pOUT activity, and establish that pOUT is the only IS10 promoter specifying the anti-sense RNA-OUT. (iv) The latter, however, need not be so: heterologous promoters, if properly positioned, can also specify active anti-sense RNAs. (v) These heterologously promoted anti-sense RNAs are processed to species closely resembling native RNA-OUT.
对影响IS10启动子pIN和pOUT的11个突变进行遗传分析,这些启动子参与转座酶基因表达的反义RNA调控,并对转录本进行表征,结果表明:(i) 在体内已明确鉴定出转座酶信息(RNA-IN)和反义RNA(RNA-OUT)。(ii) 五个突变影响pIN活性,并确定pIN是唯一转录tnp基因的IS10启动子,也是唯一对DNA腺嘌呤甲基化有反应的此类IS10启动子。(iii) 六个突变改变pOUT活性,并确定pOUT是唯一指定反义RNA-OUT的IS10启动子。(iv) 然而,情况不一定如此:如果位置合适,异源启动子也可以指定有活性的反义RNA。(v) 这些异源启动的反义RNA被加工成与天然RNA-OUT非常相似的物种。