Bechhofer D H, Wang W
Department of Biochemistry, Mount Sinai School of Medicine of the City University of New York, New York, New York 10029, USA.
J Bacteriol. 1998 Nov;180(22):5968-77. doi: 10.1128/JB.180.22.5968-5977.1998.
ermC mRNA decay was examined in a mutant of Bacillus subtilis that has a deleted pnpA gene (coding for polynucleotide phosphorylase). 5'-proximal RNA fragments less than 400 nucleotides in length were abundant in the pnpA strain but barely detectable in the wild type. On the other hand, the patterns of 3'-proximal RNA fragments were similar in the wild-type and pnpA strains. Northern blot analysis with different probes showed that the 5' end of the decay intermediates was the native ermC 5' end. For one prominent ermC RNA fragment, in particular, it was shown that formation of its 3' end was directly related to the presence of a stalled ribosome. 5'-proximal decay intermediates were also detected for transcripts encoded by the yybF gene. These results suggest that PNPase activity, which may be less sensitive to structures or sequences that block exonucleolytic decay, is required for efficient decay of specific mRNA fragments. However, it was shown that even PNPase activity could be blocked in vivo at a particular RNA structure.
在枯草芽孢杆菌的一个缺失pnpA基因(编码多核苷酸磷酸化酶)的突变体中检测了ermC mRNA的衰变情况。在pnpA菌株中,长度小于400个核苷酸的5'-近端RNA片段大量存在,但在野生型中几乎检测不到。另一方面,野生型和pnpA菌株中3'-近端RNA片段的模式相似。用不同探针进行的Northern印迹分析表明,衰变中间体的5'端是天然的ermC 5'端。特别是对于一个突出的ermC RNA片段,已表明其3'端的形成与停滞核糖体的存在直接相关。对于yybF基因编码的转录本也检测到了5'-近端衰变中间体。这些结果表明,高效衰变特定mRNA片段需要PNPase活性,该活性可能对阻碍核酸外切衰变的结构或序列不太敏感。然而,已表明即使是PNPase活性在体内也可能在特定RNA结构处被阻断。