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SAM 响应性 S(MK)框是一种可逆的核酶。

The SAM-responsive S(MK) box is a reversible riboswitch.

机构信息

Department of Microbiology, The Ohio State University, Columbus, OH 43210, USA.

出版信息

Mol Microbiol. 2010 Dec;78(6):1393-402. doi: 10.1111/j.1365-2958.2010.07410.x. Epub 2010 Oct 18.

Abstract

The S(MK) (SAM-III) box is an S-adenosylmethionine (SAM)-responsive riboswitch found in the 5' untranslated region of metK genes, encoding SAM synthetase, in many members of the Lactobacillales. SAM binding causes a structural rearrangement in the RNA that sequesters the Shine-Dalgarno (SD) sequence by pairing with a complementary anti-SD (ASD) sequence; sequestration of the SD sequence inhibits binding of the 30S ribosomal subunit and prevents translation initiation. We observed a slight increase in the half-life of the metK transcript in vivo when Enterococcus faecalis cells were depleted for SAM, but no significant change in overall transcript abundance, consistent with the model that this riboswitch regulates at the level of translation initiation. The half-life of the SAM-S(MK) box RNA complex in vitro is shorter than that of the metK transcript in vivo, raising the possibility of reversible binding of SAM. We used a fluorescence assay to directly visualize reversible switching between the SAM-free and SAM-bound conformations. We propose that the S(MK) box riboswitch can make multiple SAM-dependent regulatory decisions during the lifetime of the transcript in vivo, acting as a reversible switch that allows the cell to respond rapidly to fluctuations in SAM pools by modulating expression of the SAM synthetase gene.

摘要

S(MK)(SAM-III)盒是一种 S-腺苷甲硫氨酸(SAM)反应性的 RNA 分子,存在于许多乳杆菌目成员的 metK 基因 5'非翻译区。SAM 结合导致 RNA 发生结构重排,通过与互补的反 Shine-Dalgarno(ASD)序列配对来隔离 Shine-Dalgarno(SD)序列;SD 序列的隔离抑制了 30S 核糖体亚基的结合,并阻止了翻译起始。当粪肠球菌细胞 SAM 耗尽时,我们观察到体内 metK 转录本的半衰期略有增加,但总体转录丰度没有显著变化,这与该核糖开关在翻译起始水平调节的模型一致。体外 SAM-S(MK)盒 RNA 复合物的半衰期短于体内 metK 转录本的半衰期,这增加了 SAM 可逆结合的可能性。我们使用荧光测定法直接可视化 SAM 自由和 SAM 结合构象之间的可逆转换。我们提出,S(MK)盒核糖开关可以在体内转录本的寿命内做出多个依赖 SAM 的调节决定,作为一个可逆开关,使细胞能够通过调节 SAM 合成酶基因的表达,快速响应 SAM 池的波动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ff/3064258/47933016b1fd/nihms251175f1.jpg

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