Proteomic identification of tmRNA substrates

Sue Jean Hong, Faith H. Lessner, Elisabeth M. Mahen, Kenneth C. Keiler

Research output: Contribution to journalArticle

23 Scopus citations

Abstract

The tmRNA-SmpB system releases ribosomes stalled on truncated mRNAs and tags the nascent polypeptides to target them for proteolysis. In many species, mutations that disrupt tmRNA activity cause defects in growth or development. In Caulobacter crescentus cells lacking tmRNA activity there is a delay in the initiation of DNA replication, which disrupts the cell cycle. To understand the molecular basis for this phenotype, 73 C. crescentus proteins were identified that are tagged by tmRNA under normal growth conditions. Among these substrates, proteins involved in DNA replication, recombination, and repair were overrepresented, suggesting that misregulation of these factors in the absence of tmRNA activity might be responsible for the delay in initiation of DNA replication. Analysis of the tagging sites within these substrates revealed a conserved nucleotide motif 5′ of the tagging site, which is required for wild-type tmRNA tagging.

Original languageEnglish (US)
Pages (from-to)17128-17133
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume104
Issue number43
DOIs
StatePublished - Oct 23 2007

All Science Journal Classification (ASJC) codes

  • General

Fingerprint Dive into the research topics of 'Proteomic identification of tmRNA substrates'. Together they form a unique fingerprint.

  • Cite this