The aptamer core of SAM-IV riboswitches mimics the ligand-binding site of SAM-I riboswitches

被引:85
作者
Weinberg, Zasha [1 ]
Regulski, Elizabeth E. [1 ]
Hammond, Ming C. [2 ]
Barrick, Jeffrey E. [2 ,3 ]
Yao, Zizhen [4 ]
Ruzzo, Walter L. [4 ,5 ]
Breaker, Ronald R. [1 ,2 ,3 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Yale Univ, Howard Hughes Med Inst, New Haven, CT 06520 USA
[3] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[4] Univ Washington, Dept Comp Sci & Engn, Seattle, WA 98195 USA
[5] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
关键词
AdoMet; S-adenosylmethionine; riboswitches; scaffold; Streptomyces;
D O I
10.1261/rna.988608
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
A novel family of riboswitches, called SAM-IV, is the fourth distinct set of mRNA elements to be reported that regulate gene expression via direct sensing of S-adenosylmethionine (SAM or AdoMet). SAM-IV riboswitches share conserved nucleotide positions with the previously described SAM-I riboswitches, despite rearranged structures and nucleotide positions with family-specific nucleotide identities. Sequence analysis and molecular recognition experiments suggest that SAM-I and SAM-IV riboswitches share similar ligand binding sites, but have different scaffolds. Our findings support the view that RNA has considerable structural versatility and reveal that riboswitches exploit this potential to expand the scope of RNA in genetic regulation.
引用
收藏
页码:822 / 828
页数:7
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