Literature DB >> 16775783

cry1Aa lacks stability elements at its 5'-UTR but integrity of its transcription terminator is critical to prevent decay of its transcript.

Jorge Humberto Ramírez-Prado1, Eva Isabel Martínez-Márquez, Gabriela Olmedo-Alvarez.   

Abstract

We analyzed the influence of the 5' and 3' untranslated regions of the Bacillus thuringiensis cry1Aa on its mRNA stability. Although the cry1Aa gene has a stable transcript (8 min), its 5' UTR did not provide stability to the reporter gene uidA. Stability of cry1Aa could be increased to 40 min by addition of an SP82 stability element at the 5' UTR, suggesting that once the 5' and 3' ends were protected initiation of decay could be effectively blocked. We generated mutations in the transcription terminator and found that changes that reduced the stability of the stem, a larger loop, or elimination of the U-trail sharply decreased the half-life of the transcript. Therefore, unlike some stable bacterial transcripts, cry1Aa lacks special features at the end 5' to prevent decay, but its terminator is the main determinant of its stability.

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Year:  2006        PMID: 16775783     DOI: 10.1007/s00284-005-5178-1

Source DB:  PubMed          Journal:  Curr Microbiol        ISSN: 0343-8651            Impact factor:   2.188


  27 in total

1.  An efficient Shine-Dalgarno sequence but not translation is necessary for lacZ mRNA stability in Escherichia coli.

Authors:  L A Wagner; R F Gesteland; T J Dayhuff; R B Weiss
Journal:  J Bacteriol       Date:  1994-03       Impact factor: 3.490

2.  mRNA stabilization by the ompA 5' untranslated region: two protective elements hinder distinct pathways for mRNA degradation.

Authors:  T E Arnold; J Yu; J G Belasco
Journal:  RNA       Date:  1998-03       Impact factor: 4.942

3.  Differential contributions of two elements of rho-independent terminator to transcription termination and mRNA stabilization.

Authors:  H Abe; H Aiba
Journal:  Biochimie       Date:  1996       Impact factor: 4.079

4.  Mechanism of decay of the cry1Aa mRNA in Bacillus subtilis.

Authors:  C Vázquez-Cruz; G Olmedo-Alvarez
Journal:  J Bacteriol       Date:  1997-10       Impact factor: 3.490

5.  Transcriptional and translational start sites for the Bacillus thuringiensis crystal protein gene.

Authors:  H C Wong; H E Schnepf; H R Whiteley
Journal:  J Biol Chem       Date:  1983-02-10       Impact factor: 5.157

6.  Construction of gusA transcriptional fusion vectors for Bacillus subtilis and their utilization for studies of spore formation.

Authors:  M L Karow; P J Piggot
Journal:  Gene       Date:  1995-09-22       Impact factor: 3.688

7.  Construction of a cloning site near one end of Tn917 into which foreign DNA may be inserted without affecting transposition in Bacillus subtilis or expression of the transposon-borne erm gene.

Authors:  P Youngman; J B Perkins; R Losick
Journal:  Plasmid       Date:  1984-07       Impact factor: 3.466

8.  A 5' stem-loop and ribosome binding but not translation are important for the stability of Bacillus subtilis aprE leader mRNA.

Authors:  Gustav Hambraeus; Kaisa Karhumaa; Blanka Rutberg
Journal:  Microbiology       Date:  2002-06       Impact factor: 2.777

9.  The stability of mRNA from the gsiB gene of Bacillus subtilis is dependent on the presence of a strong ribosome binding site.

Authors:  B Jürgen; T Schweder; M Hecker
Journal:  Mol Gen Genet       Date:  1998-06

10.  Maturation of Escherichia coli tryptophan operon mRNA: evidence for 3' exonucleolytic processing after rho-dependent termination.

Authors:  J E Mott; J L Galloway; T Platt
Journal:  EMBO J       Date:  1985-07       Impact factor: 11.598

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