Literature DB >> 6373018

An E. coli DNA fragment 118 base pairs in length provides dnaY+ complementing activity.

D A Mullin, G M Garcia, J R Walker.   

Abstract

The dnaY gene of E. coli, thought to be involved in the polymerization phase of DNA replication, was localized on a fragment 118 base pairs in length. This fragment, cloned in two different vectors and tested in a dnaY (Ts) recA host, has dnaY + complementing activity. The nucleotide sequence of the 118 base pairs and flanking bases was determined. The dnaY complementing activity was inactivated by transposon insertion and by localized chemical mutagenesis. Three independent insertions of Tn5 into the 118 base pair region eliminated dnaY activity. Eight single-base-change mutations that resulted in loss of dnaY activity also were located within the 118 base pair region. Analysis of the nucleotide sequence reveals a potential promoter but reveals no open reading frames likely to be translated into polypeptides. However, an RNA transcript of the dnaY region is synthesized in vivo. Perhaps the active product of dnaY is a small RNA or perhaps the dnaY region functions as a site.

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Year:  1984        PMID: 6373018     DOI: 10.1016/0092-8674(84)90399-4

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  11 in total

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Authors:  P Saxena; J R Walker
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Review 2.  Structure and organization of the transfer ribonucleic acid genes of Escherichia coli K-12.

Authors:  M J Fournier; H Ozeki
Journal:  Microbiol Rev       Date:  1985-12

Review 3.  Nucleolytic processing of ribonucleic acid transcripts in procaryotes.

Authors:  T C King; R Sirdeskmukh; D Schlessinger
Journal:  Microbiol Rev       Date:  1986-12

4.  Nonessential region of bacteriophage P4: DNA sequence, transcription, gene products, and functions.

Authors:  D Ghisotti; S Finkel; C Halling; G Dehò; G Sironi; R Calendar
Journal:  J Virol       Date:  1990-01       Impact factor: 5.103

5.  A minor arginine tRNA mutant limits translation preferentially of a protein dependent on the cognate codon.

Authors:  K S Chen; T C Peters; J R Walker
Journal:  J Bacteriol       Date:  1990-05       Impact factor: 3.490

6.  The additional guanylate at the 5' terminus of Escherichia coli tRNAHis is the result of unusual processing by RNase P.

Authors:  O Orellana; L Cooley; D Söll
Journal:  Mol Cell Biol       Date:  1986-02       Impact factor: 4.272

7.  tRNA(Arg) (fimU) and expression of SEF14 and SEF21 in Salmonella enteritidis.

Authors:  S C Clouthier; S K Collinson; A P White; P A Banser; W W Kay
Journal:  J Bacteriol       Date:  1998-02       Impact factor: 3.490

8.  Characterization of the cryptic lambdoid prophage DLP12 of Escherichia coli and overlap of the DLP12 integrase gene with the tRNA gene argU.

Authors:  D F Lindsey; D A Mullin; J R Walker
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

9.  The Escherichia coli argU10(Ts) phenotype is caused by a reduction in the cellular level of the argU tRNA for the rare codons AGA and AGG.

Authors:  Kensaku Sakamoto; Satoshi Ishimaru; Takatsugu Kobayashi; James R Walker; Shigeyuki Yokoyama
Journal:  J Bacteriol       Date:  2004-09       Impact factor: 3.490

10.  Structure and transcription of the tRNAPro1 gene from Escherichia coli.

Authors:  Y Kuchino; F Mori; S Nishimura
Journal:  Nucleic Acids Res       Date:  1985-05-10       Impact factor: 16.971

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