Literature DB >> 2443706

Transcription products from the rplKAJL-rpoBC gene cluster.

W L Downing1, P P Dennis.   

Abstract

Transcripts from the rplKAJL-rpoBC ribosomal protein-RNA polymerase gene cluster have been quantified and their ends mapped using RNA-DNA hybridization, sucrose density-gradient sedimentation, Northern hybridization and S1 nuclease protection. The results indicate that the most abundant transcript is the 2600 nucleotide tetracistronic L11-L1-L10-L12 mRNA initiated at the upstream major PL11 promoter and terminated at the transcription attenuator in the L12-beta intergenic space. Somewhat less abundant 1300 nucleotide L11-L1 and L10-L12 bicistronic transcripts were observed. The 3' ends of the L11-L1 transcripts were heterogeneous; most of the ends were localized to three sites within a 110 base-pair region in the L1-L10 intergenic space. This intergenic space encodes also the major PL10 promoter and the mRNA binding site for the L10 translational control protein. Two 5' ends were observed for L10-L12 bicistronic mRNA, one at the PL10 promoter and the other 150 nucleotides further downstream in a region in which promoter activity has not been detected. It is suggested that this second downstream 5' end is generated by processing of the transcripts initiated at the major PL10 promoter. No transcript initiation in the L10-L12 intergenic space was detected. About 80% of the transcripts reading through the L12 gene were terminated in the vicinity of the transcription attenuator that is responsible for the reduction in the expression of the downstream RNA polymerase genes. Transcripts reading through the attenuator were partially processed by RNase III within a potential hairpin structure in the RNA transcript. Processing appears to produce 3' and 5' transcript end sites separated by about ten nucleotides. No other major 5' ends were observed in the L12-beta intergenic space. These results indicate that the two major promoters, PL11 and PL10, are both utilized to drive the interrelated transcriptional expression of this ribosomal protein-RNA polymerase gene cluster.

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Year:  1987        PMID: 2443706     DOI: 10.1016/0022-2836(87)90238-5

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  17 in total

1.  Transcription frequency modulates the efficiency of an attenuator preceding the rpoBC RNA polymerase genes of Escherichia coli: possible autogenous control.

Authors:  K L Steward; T Linn
Journal:  Nucleic Acids Res       Date:  1992-09-25       Impact factor: 16.971

2.  Autogenous regulation of the RNA polymerase beta subunit of Escherichia coli occurs at the translational level in vivo.

Authors:  L Passador; T Linn
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

Review 3.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

4.  Sequence and transcriptional pattern of the essential Escherichia coli secE-nusG operon.

Authors:  W L Downing; S L Sullivan; M E Gottesman; P P Dennis
Journal:  J Bacteriol       Date:  1990-03       Impact factor: 3.490

5.  Improved vector system for constructing transcriptional fusions that ensures independent translation of lacZ.

Authors:  T Linn; R St Pierre
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

Review 6.  Linkage map of Escherichia coli K-12, edition 8.

Authors:  B J Bachmann
Journal:  Microbiol Rev       Date:  1990-06

7.  Sequence alignment and evolutionary comparison of the L10 equivalent and L12 equivalent ribosomal proteins from archaebacteria, eubacteria, and eucaryotes.

Authors:  L C Shimmin; C Ramirez; A T Matheson; P P Dennis
Journal:  J Mol Evol       Date:  1989-11       Impact factor: 2.395

8.  The genome of the non-cultured, bacterial-like organism associated with citrus greening disease contains the nusG-rplKAJL-rpoBC gene cluster and the gene for a bacteriophage type DNA polymerase.

Authors:  S Villechanoux; M Garnier; F Laigret; J Renaudin; J M Bové
Journal:  Curr Microbiol       Date:  1993-03       Impact factor: 2.188

9.  Measurement of the rates of synthesis of three components of ribosomes of Mycobacterium fortuitum: a theoretical approach to qRT-PCR experimentation.

Authors:  Maria Jesus Garcia; Maria Carmen Nuñez; Robert Ashley Cox
Journal:  PLoS One       Date:  2010-07-14       Impact factor: 3.240

10.  Evolutionary relationships among eubacteria, cyanobacteria, and chloroplasts: evidence from the rpoC1 gene of Anabaena sp. strain PCC 7120.

Authors:  K J Bergsland; R Haselkorn
Journal:  J Bacteriol       Date:  1991-06       Impact factor: 3.490

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