Neuhaus Klaus, Anastasov Natasa, Kaberdin Vladimir, Francis Kevin P, Miller Virginia L, Scherer Siegfried
Department of Molecular Microbiology, Washington University in St Louis, St Louis, MO 63110, USA.
Mol Microbiol. 2003 Dec;50(5):1629-45. doi: 10.1046/j.1365-2958.2003.03795.x.
Acclimatization of the psychrotolerant Yersinia enterocolitica after a cold shock from 30 degrees C to 10 degrees C causes transcription of the major cold shock protein (CSP) bicistronic gene cspA1/A2 to increase by up to 300-fold. Northern blot analysis of cspA1/A2 using four probes that hybridize specifically to different regions of CSP mRNA revealed the appearance of a number of cspA1/A2 transcripts that are smaller than the original transcript and transiently visible at the end of the acclimation period. Primer extension and RNA protection experiments demonstrated that these smaller mRNAs have 5' ends located in the same core sequence (5'-AGUAAA-3') at five different places within the mRNA, indicating preferential cleavage of the CSP mRNA transcripts. A similar result was obtained for cspB of Escherichia coli, containing two such core sequences. Furthermore, this motif is present in the major CSP genes of a variety of Gram-negative and Gram-positive bacteria. We have therefore termed this sequence cold shock cut box (CSC-box). After inserting a CSC-box into a plasmid-bound lacZ gene in Y. enterocolitica, the mRNA of this construct was cleaved within the CSC-box, and a change in this CSC-box from AGUAAA to AGUCCC dramatically reduced cleavage of the mutated lacZ gene. Mutating all CSC-boxes in Y. enterocolitica of a plasmid bound cspA1/A2 dramatically increases the lag time after a cold shock before re-growth occurs. Based on these results, we suggest that the role of the CSC-box is related to downregulation of cspA mRNA after acclimation to low temperature.
嗜冷小肠结肠炎耶尔森菌从30℃冷休克至10℃后的适应性变化会使主要冷休克蛋白(CSP)双顺反子基因cspA1/A2的转录增加多达300倍。使用四个与CSP mRNA不同区域特异性杂交的探针进行的cspA1/A2 Northern印迹分析显示,出现了一些比原始转录本小的cspA1/A2转录本,并且在适应期结束时短暂可见。引物延伸和RNA保护实验表明,这些较小的mRNA在mRNA内五个不同位置的5'端位于相同的核心序列(5'-AGUAAA-3')中,表明CSP mRNA转录本存在优先切割。对于含有两个此类核心序列的大肠杆菌cspB,也获得了类似的结果。此外,该基序存在于多种革兰氏阴性和革兰氏阳性细菌的主要CSP基因中。因此,我们将此序列称为冷休克切割框(CSC-box)。在小肠结肠炎耶尔森菌中将一个CSC-box插入与质粒结合的lacZ基因后,该构建体的mRNA在CSC-box内被切割,并且该CSC-box从AGUAAA变为AGUCCC会显著降低突变的lacZ基因的切割。将与质粒结合的cspA1/A2的小肠结肠炎耶尔森菌中的所有CSC-box突变会显著增加冷休克后重新生长前的延迟时间。基于这些结果,我们认为CSC-box的作用与低温适应后cspA mRNA的下调有关。