Literature DB >> 7041118

Effects of DNA base analogs on transcription termination at the tryptophan operon attenuator of EScherichia coli.

P J Farnham, T Platt.   

Abstract

We have devised a method to specifically incorporate deoxyribonucleotide base analogs in vitro into either strand of the tryptophan (trp) operon attenuator region, using primed synthesis on bacteriophage M13 derivatives carrying cloned trp attenuator DNA. We have employed these techniques to extend previous studies implicating both RNA-RNA and RNA-DNA interactions in transcription termination in an attempt to determine the nature of the contribution from the template DNA molecule in termination regions. In general, we find that the dramatic effects upon transcription termination seen with base analog incorporation into mRNA do not occur when similar analogs are incorporated into the DNA. Only the analog 2,6-diaminopurine deoxyribonucleotide triphosphate (dDapTP), which strengthens A.T or A.U base pairing, elicits a significant response: in the template DNA strand, the presence of this analog increases read-through at the trp attenuator. The analog 5-bromouracil deoxyribonucleoside triphosphate (BrdUTP), which also strengthens pairing with its complementary base, has no detectable effect on termination when it is placed in either strand of the trp attenuator or the mutant attenuator trp a1419. Surprisingly, though the analog 5-iodocytosine deoxyribonucleoside triphosphate (IdCTP) does not affect termination, it has a great effect on initiation of transcription, depressing trp promoter activity as well as stimulating transcription from other regions. These results support the postulated interaction between terminal uridines in mRNA and the template DNA strand in enhancing termination and suggest that there are no significant additional contributions from the DNA. In addition, the novel use of M13 derivatives for incorporating analogs into the DNA on a preparative scale provides a technique for introducing mutations in a general but controlled fashion as a new means for studying other regulatory regions.

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Year:  1982        PMID: 7041118      PMCID: PMC345886          DOI: 10.1073/pnas.79.4.998

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  16 in total

Review 1.  Regulatory sequences involved in the promotion and termination of RNA transcription.

Authors:  M Rosenberg; D Court
Journal:  Annu Rev Genet       Date:  1979       Impact factor: 16.830

2.  Transcription of T7 DNA containing modified nucleotides by bacteriophage T7 specific RNA polymerase.

Authors:  S J Stahl; M J Chamberlin
Journal:  J Biol Chem       Date:  1978-07-25       Impact factor: 5.157

3.  Termination of transcription by Escherichia coli RNA polymerase in vitro is affected by ribonucleoside triphosphate base analogs.

Authors:  N F Neff; M J Chamberlin
Journal:  J Biol Chem       Date:  1978-04-10       Impact factor: 5.157

4.  A fast and simple method for sequencing DNA cloned in the single-stranded bacteriophage M13.

Authors:  P H Schreier; R Cortese
Journal:  J Mol Biol       Date:  1979-03-25       Impact factor: 5.469

5.  Methylation of single-stranded DNA in vitro introduces new restriction endonuclease cleavage sites.

Authors:  B Gronenborn; J Messing
Journal:  Nature       Date:  1978-03-23       Impact factor: 49.962

6.  A procedure for the rapid, large-scall purification of Escherichia coli DNA-dependent RNA polymerase involving Polymin P precipitation and DNA-cellulose chromatography.

Authors:  R R Burgess; J J Jendrisak
Journal:  Biochemistry       Date:  1975-10-21       Impact factor: 3.162

7.  The attenuator of the tryptophan operon in E.coli: rho-mediated release of RNA polymerase from a transcription termination complex in vitro.

Authors:  R S Fuller; T Platt
Journal:  Nucleic Acids Res       Date:  1978-12       Impact factor: 16.971

8.  Termination of transcription by Escherichia coli RNA polymerase: influence of secondary structure of RNA transcripts on rho-independent and rho-dependent termination.

Authors:  S Adhya; P Sarkar; D Valenzuela; U Maitra
Journal:  Proc Natl Acad Sci U S A       Date:  1979-04       Impact factor: 11.205

9.  Transcription termination at the trp operon attenuators of Escherichia coli and Salmonella typhimurium: RNA secondary structure and regulation of termination.

Authors:  F Lee; C Yanofsky
Journal:  Proc Natl Acad Sci U S A       Date:  1977-10       Impact factor: 11.205

10.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

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2.  Functional analysis of mutations in the transcription terminator T1 that suppress two dnaG alleles in Escherichia coli.

Authors:  R A Britton; J R Lupski
Journal:  Mol Gen Genet       Date:  1995-03-20

3.  Use of complementary DNA oligomers to probe trp leader transcript secondary structures involved in transcription pausing and termination.

Authors:  R Fisher; C Yanofsky
Journal:  Nucleic Acids Res       Date:  1984-04-11       Impact factor: 16.971

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Authors:  Jing Yun A Zhu; Irmtraud M Meyer
Journal:  RNA Biol       Date:  2015       Impact factor: 4.652

5.  Influence of major-groove chemical modifications of DNA on transcription by bacterial RNA polymerases.

Authors:  Veronika Raindlová; Martina Janoušková; Michaela Slavíčková; Pavla Perlíková; Soňa Boháčová; Nemanja Milisavljevič; Hana Šanderová; Martin Benda; Ivan Barvík; Libor Krásný; Michal Hocek
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