Ranade K, Poteete A R
Department of Molecular Genetics and Microbiology, University of Massachusetts, Worcester 01655.
Genes Dev. 1993 Aug;7(8):1498-507. doi: 10.1101/gad.7.8.1498.
Antisense RNAs regulate expression of target genes in a variety of ways--transcription termination, translation initiation, and mRNA stability. We describe a case in which the target gene encodes two polypeptides, and antisense RNA causes a switch in its translation by selectively inhibiting synthesis of one of the polypeptides. Bacteriophage P22 is a temperate Salmonella phage; in the prophage state it expresses only a handful of its genes. One of these genes, sieB, aborts the lytic development of some phages. P22 itself is insensitive to the lethal effect of SieB because it harbors a determinant called esc. We show that the sieB gene encodes two polypeptides--SieB, which is the exclusion protein, and Esc, which is a truncated version of SieB that inhibits its action. Superinfecting P22 synthesizes an antisense RNA, sas, that inhibits synthesis of SieB but allows continued synthesis of Esc, thus allowing P22 to bypass SieB-mediated exclusion. This translational switch induced by sas RNA is essential to vegetatively developing P22; a mutation that prevents this switch causes P22 to commit SieB-mediated suicide. Finally, we show that P22's Esc allows it to circumvent the SieB-mediated exclusion system of bacteriophage lambda.
反义RNA通过多种方式调控靶基因的表达——转录终止、翻译起始和mRNA稳定性。我们描述了一个案例,其中靶基因编码两种多肽,反义RNA通过选择性抑制其中一种多肽的合成导致其翻译发生转换。噬菌体P22是一种温和的沙门氏菌噬菌体;在原噬菌体状态下,它只表达少数几个基因。其中一个基因sieB会阻止某些噬菌体的裂解发育。P22本身对SieB的致死效应不敏感,因为它含有一个名为esc的决定簇。我们表明,sieB基因编码两种多肽——作为排除蛋白的SieB和作为SieB截短版本并抑制其作用的Esc。超感染的P22合成一种反义RNA,即sas,它抑制SieB的合成,但允许Esc继续合成,从而使P22能够绕过SieB介导的排除作用。由sas RNA诱导的这种翻译转换对营养生长的P22至关重要;阻止这种转换的突变会导致P22发生SieB介导的自杀。最后,我们表明P22的Esc使其能够规避噬菌体λ的SieB介导的排除系统。