A SAM-I riboswitch with the ability to sense and respond to uncharged initiator tRNA.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32493973.
- Also identified by DOI 10.1038/s41467-020-16417-z and PMC identifier 7270179.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
All known riboswitches use their aptamer to senese one metabolite signal and their expression platform to regulate gene expression. Here, we characterize a SAM-I riboswitch (SAM-I<sub>Xcc</sub>) from the Xanthomonas campestris that regulates methionine synthesis via the met operon. In vitro and in vivo experiments show that SAM-I<sub>Xcc</sub> controls the met operon primarily at the translational level in response to cellular S-adenosylmethionine (SAM) levels. Biochemical and genetic data demonstrate that SAM-I<sub>Xcc</sub> expression platform not only can repress gene expression in response to SAM binding to SAM-I<sub>Xcc</sub> aptamer but also can sense and bind uncharged initiator Met tRNA, resulting in the sequestering of the anti-Shine-Dalgarno (SD) sequence and freeing the SD for translation initiation. These findings identify a SAM-I riboswitch with a dual functioning expression platform that regulates methionine synthesis through a previously unrecognized mechanism and discover a natural tRNA-sensing RNA element. This SAM-I riboswitch appears to be highly conserved in Xanthomonas species.
Medical subject headings
- RNA, Transfer, Met
- Riboswitch
- S-Adenosylmethionine