Literature DB >> 2494447

Use of supF, an Escherichia coli tyrosine suppressor tRNA gene, as a mutagenic target in shuttle-vector plasmids.

K H Kraemer1, M M Seidman.   

Abstract

The Escherichia coli tyrosine amber suppressor tRNA gene, supF, has been utilized as a mutagenic target in several shuttle-vector plasmids. Data on mutagenic inactivation of suppressor activity was obtained from induced mutagenesis experiments with plasmids pZ189 and p3AC, and from studies on alterations of the supF gene transduced into E. coli. 162 single or tandem base-substitution mutations that reduce or eliminate suppressor activity were identified at 86 sites within 158 base pairs. The 2 transition and 4 transversion mutations possible in double-stranded DNA were all detectable. At 56 sites two different inactivating mutations were found; and at 20 sites all 3 possible base substitution mutations inactivated suppressor function. Most of the mutations were clustered within the mature tRNA region: 144 of the base-substitution mutations were found at 74 sites within the 85-bp mature tRNA region. Insertions of 1 or 2 bases at 4 sites and deletions of 1 to 3 bases at 15 sites were found to inactivate supF function. A few silent mutations which do not inactivate suppressor function were found: single base-substitutions at 4 sites, 14 pairs of silent double mutations, and a large deletion including the promoter region. The supF gene is thus an extremely sensitive target for mutagenic inactivation in shuttle-vector plasmids.

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Year:  1989        PMID: 2494447     DOI: 10.1016/0165-1110(89)90011-0

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  24 in total

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2.  Fluorescence-based directed termination PCR: direct mutation characterization without sequencing.

Authors:  J Z Chen; L Smith; G P Pfeifer; G P Holmquist
Journal:  Nucleic Acids Res       Date:  2001-02-15       Impact factor: 16.971

3.  Non-B DNA-forming sequences and WRN deficiency independently increase the frequency of base substitution in human cells.

Authors:  Albino Bacolla; Guliang Wang; Aklank Jain; Nadia A Chuzhanova; Regina Z Cer; Jack R Collins; David N Cooper; Vilhelm A Bohr; Karen M Vasquez
Journal:  J Biol Chem       Date:  2011-02-01       Impact factor: 5.157

4.  Construction of a supF-based system for detection of mutations in the chromosomal DNA of Arabidopsis.

Authors:  Keiichiro Hiratsu; Shiori Shiotani; Kozo Makino; Tatsuo Nunoshiba
Journal:  Mol Genet Genomics       Date:  2013-10-24       Impact factor: 3.291

5.  Mutagenic specificities of four stereoisomeric benzo[c]phenanthrene dihydrodiol epoxides.

Authors:  C A Bigger; J St John; H Yagi; D M Jerina; A Dipple
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-01       Impact factor: 11.205

6.  Mutagenesis and repair induced by the DNA advanced glycation end product N2-1-(carboxyethyl)-2'-deoxyguanosine in human cells.

Authors:  Daniel Tamae; Punnajit Lim; Gerald E Wuenschell; John Termini
Journal:  Biochemistry       Date:  2011-02-28       Impact factor: 3.162

7.  DNA polymerase POLN participates in cross-link repair and homologous recombination.

Authors:  George-Lucian Moldovan; Mahesh V Madhavan; Kanchan D Mirchandani; Ryan M McCaffrey; Patrizia Vinciguerra; Alan D D'Andrea
Journal:  Mol Cell Biol       Date:  2009-12-07       Impact factor: 4.272

8.  High-resolution functional mapping of a cloned gene by genetic footprinting.

Authors:  I R Singh; R A Crowley; P O Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1997-02-18       Impact factor: 11.205

9.  Comparative mutagenicities of N6-methoxy-2,6-diaminopurine and N6-methoxyaminopurine 2'-deoxyribonucleosides and their 5'-triphosphates.

Authors:  F Hill; D M Williams; D Loakes; D M Brown
Journal:  Nucleic Acids Res       Date:  1998-03-01       Impact factor: 16.971

10.  Hydrogen peroxide induces G:C to T:A and G:C to C:G transversions in the supF gene of Escherichia coli.

Authors:  S Akasaka; K Yamamoto
Journal:  Mol Gen Genet       Date:  1994-06-03
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