Hostname: page-component-cd9895bd7-q99xh Total loading time: 0 Render date: 2024-12-24T13:57:20.309Z Has data issue: false hasContentIssue false

The GA motif: An RNA element common to bacterial antitermination systems, rRNA, and eukaryotic RNAs

Published online by Cambridge University Press:  27 July 2001

WADE C. WINKLER
Affiliation:
Department of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA
FRANK J. GRUNDY
Affiliation:
Department of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA
BROOKE A. MURPHY
Affiliation:
Department of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA
TINA M. HENKIN
Affiliation:
Department of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA
Get access

Abstract

Two different transcription termination control mechanisms, the T box and S box systems, are used to regulate transcription of many bacterial aminoacyl-tRNA synthetase, amino acid biosynthesis, and amino acid transport genes. Both of these regulatory mechanisms involve an untranslated mRNA leader region capable of adopting alternate structural conformations that result in transcription termination or transcription elongation into the downstream region. Comparative analyses revealed a small RNA secondary structural element, designated the GA motif, that is highly conserved in both T box and S box leader sequences. The motif consists of two short helices separated by an asymmetric internal loop, with highly conserved GA dinucleotide sequences on either side of the internal loop. Site-directed mutagenesis of this motif in model T and S box leader sequences indicated that it is essential for transcriptional regulation in both systems. This motif is similar to the binding site of yeast ribosomal protein L30, the Snu13p binding sites found in U4 snRNA and box C/D snoRNAs, and two elements in 23S rRNA.

Type
Research Article
Copyright
© 2001 RNA Society

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)