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5'-非翻译区参与多变鱼腥藻M3中rbpA1基因的冷调节表达。

Involvement of the 5'-untranslated region in cold-regulated expression of the rbpA1 gene in the cyanobacterium Anabaena variabilis M3.

作者信息

Sato N, Nakamura A

机构信息

Department of Biochemistry and Molecular Biology, Faculty of Science, Saitama University, Urawa 338, Japan.

出版信息

Nucleic Acids Res. 1998 May 1;26(9):2192-9. doi: 10.1093/nar/26.9.2192.

Abstract

Transcript of the rbpA1 gene in Anabaena variabilis accumulates significantly at low growth temperatures below 28 degreesC. This accumulation was maximal at 16 degreesC. Accumulation of the rbpA1 transcript was completely abolished by rifampicin, but not by chloramphenicol. Photosynthesis was not required for this cold-induced accumulation. This accumulation of transcript was partly accounted for by increased stability of the rbpA1 transcript at low temperature. Expression of chimeric genes containing 3'-deleted rbpA1 sequences fused to the lacZ gene was regulated by low temperature when almost the entire 5'-untranslated region (5'-UTR) remained undeleted. Further deletion resulted in constitutive expression of the chimeric gene. The 5'-UTR sequence formed two types of complexes in vitro with protein extract from cells grown at 38 degreesC, but not with extract from the 22 degreesC grown cells. Affinity purification identified polypeptides of 75 and 32 kDa in Complex 1 and a 72 kDa polypeptide in Complex 2. These results are compatible with a model in which expression of the rbpA1 gene is regulated by transcriptional derepression at low temperature, although additional mechanisms, such as regulation of mRNA stability, might also contribute to temperature-dependent regulation.

摘要

多变鱼腥藻中rbpA1基因的转录本在低于28℃的低温生长条件下显著积累。这种积累在16℃时达到最大值。rbpA1转录本的积累被利福平完全消除,但氯霉素不能消除。这种冷诱导积累不需要光合作用。转录本的这种积累部分是由于rbpA1转录本在低温下稳定性增加。当几乎整个5'-非翻译区(5'-UTR)未被删除时,含有与lacZ基因融合的3'-缺失rbpA1序列的嵌合基因的表达受低温调节。进一步删除导致嵌合基因的组成型表达。5'-UTR序列在体外与38℃生长的细胞的蛋白质提取物形成两种类型的复合物,但与22℃生长的细胞的提取物不形成复合物。亲和纯化鉴定出复合物1中的75 kDa和32 kDa多肽以及复合物2中的72 kDa多肽。这些结果与一个模型相符,在该模型中rbpA1基因的表达在低温下通过转录去抑制进行调节,尽管其他机制,如mRNA稳定性的调节,也可能有助于温度依赖性调节。

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