Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
14
pubmed:dateCreated
1996-8-29
pubmed:abstractText
The threonyl-tRNA synthetase gene, thrS, is a member of a family of Gram-positive genes that are induced following starvation for the corresponding amino acid by a transcriptional antitermination mechanism involving the cognate uncharged tRNA. Here we show that an additional level of complexity exists in the control of the thrS gene with the mapping of an mRNA processing site just upstream of the transcription terminator in the thrS leader region. The processed RNA is significantly more stable than the full-length transcript. Under nonstarvation conditions, or following starvation for an amino acid other than threonine, the full-length thrS mRNA is more abundant than the processed transcript. However, following starvation for threonine, the thrS mRNA exists primarily in its cleaved form. This can partly be attributed to an increased processing efficiency following threonine starvation, and partly to a further, nonspecific increase in the stability of the processed transcript under starvation conditions. The increased stability of the processed RNA contributes significantly to the levels of functional RNA observed under threonine starvation conditions, previously attributed solely to antitermination. Finally, we show that processing is likely to occur upstream of the terminator in the leader regions of at least four other genes of this family, suggesting a widespread conservation of this phenomenon in their control.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-1370426, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-1379177, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-1577690, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-2115870, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-2449287, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-2992951, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-3521892, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-7476165, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-7527891, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-8088508, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-8288542, http://linkedlifedata.com/resource/pubmed/commentcorrection/8692931-8348614
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
9
pubmed:volume
93
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6992-7
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:8692931-Amino Acyl-tRNA Synthetases, pubmed-meshheading:8692931-Bacillus subtilis, pubmed-meshheading:8692931-Base Sequence, pubmed-meshheading:8692931-Gene Expression Regulation, Bacterial, pubmed-meshheading:8692931-Gene Expression Regulation, Enzymologic, pubmed-meshheading:8692931-Genes, Bacterial, pubmed-meshheading:8692931-Kinetics, pubmed-meshheading:8692931-Molecular Sequence Data, pubmed-meshheading:8692931-Nucleic Acid Conformation, pubmed-meshheading:8692931-Polymerase Chain Reaction, pubmed-meshheading:8692931-RNA, Messenger, pubmed-meshheading:8692931-RNA-Directed DNA Polymerase, pubmed-meshheading:8692931-Recombinant Fusion Proteins, pubmed-meshheading:8692931-Rifampin, pubmed-meshheading:8692931-Terminator Regions, Genetic, pubmed-meshheading:8692931-Threonine, pubmed-meshheading:8692931-Threonine-tRNA Ligase, pubmed-meshheading:8692931-Transcription, Genetic, pubmed-meshheading:8692931-beta-Galactosidase
pubmed:year
1996
pubmed:articleTitle
Processing of the leader mRNA plays a major role in the induction of thrS expression following threonine starvation in Bacillus subtilis.
pubmed:affiliation
Unité Propre de Recherche 9073, Institut de Biologie Physic-Chimique, Paris, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't