SAM-VI RNAs selectively bind S-adenosylmethionine and exhibit similarities to SAM-III riboswitches

被引:43
作者
Arachchilage, Gayan Mirihana [1 ]
Sherlock, Madeline E. [2 ]
Weinberg, Zasha [1 ,4 ,5 ]
Breaker, Ronald R. [1 ,2 ,3 ]
机构
[1] Yale Univ, Howard Hughes Med Inst, New Haven, CT 06511 USA
[2] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT USA
[3] Yale Univ, Dept Mol Cellular & Dev Biol, KBT 506,266 Whitney Ave, New Haven, CT 06520 USA
[4] Univ Leipzig, Dept Comp Sci, Bioinformat Grp, D-04107 Leipzig, Germany
[5] Univ Leipzig, Interdisciplinary Ctr Bioinformat, D-04107 Leipzig, Germany
关键词
metK; aptamer; cofactor; gene regulation; noncoding RNA; metA; SAM; TRANSCRIPTION TERMINATION CONTROL; CANDIDATE STRUCTURED RNAS; BIOCHEMICAL VALIDATION; GENE-EXPRESSION; FREE GUANIDINE; APTAMER CLASS; BACTERIA; DIVERSITY; INTRONS; SENSE;
D O I
10.1080/15476286.2017.1399232
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Five distinct riboswitch classes that regulate gene expression in response to the cofactor S-adenosylmethionine (SAM) or its metabolic breakdown product S-adenosylhomocysteine (SAH) have been reported previously. Collectively, these SAM- or SAH-sensing RNAs constitute the most abundant collection of riboswitches, and are found in nearly every major bacterial lineage. Here, we report a potential sixth member of this pervasive riboswitch family, called SAM-VI, which is predominantly found in Bifidobacterium species. SAM-VI aptamers selectively bind the cofactor SAM and strongly discriminate against SAH. The consensus sequence and structural model for SAM-VI share some features with the consensus model for the SAM-III riboswitch class, whose members are mainly found in lactic acid bacteria. However, there are sufficient differences between the two classes such that current bioinformatics methods separately cluster representatives of the two motifs. These findings highlight the abundance of RNA structures that can form to selectively recognize SAM, and showcase the ability of RNA to utilize diverse strategies to perform similar biological functions.
引用
收藏
页码:369 / 376
页数:8
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