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Escherichia coli Strains (ndk) Lacking Nucleoside Diphosphate Kinase Are Powerful Mutators for Base Substitutions and Frameshifts in Mismatch-Repair-Deficient Strains
Author(s) -
Jeffrey H Miller,
Pauline Funchain,
Wendy M. Clendenin,
Tiffany Huang,
Anh T. H. Nguyen,
Erika M. Wolff,
Annie Yeung,
JuHuei Chiang,
Lilit Garibyan,
Malgorzata M. Slupska,
Hanjing Yang
Publication year - 2002
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/162.1.5
Subject(s) - nucleoside diphosphate kinase , biology , escherichia coli , kinase , dna mismatch repair , nucleotide , base pair , mutation , nucleoside triphosphate , nucleoside , mutant , genetics , enzyme , microbiology and biotechnology , gene , biochemistry , dna repair
Nucleoside diphosphate (NDP) kinase is one of the enzymes that maintains triphosphate pools. Escherichia coli strains (ndk) lacking this enzyme have been shown to be modest base substitution mutators, and two members of the human family of NDP kinases act as tumor suppressors. We show here that in E. coli strains lacking NDP kinase high levels of mispairs are generated, but most of these are corrected by the mismatch-repair system. Double mutants that are ndk mutS, lacking both the NDP kinase and mismatch repair, have levels of base substitutions 15-fold higher and levels of certain frameshifts up to 10-fold higher than those of the respective mutations in mutS strains that are NDP kinase proficient. A sequence analysis of the specificity of base substitution mutations generated in ndk and ndk mutS backgrounds as well as other experiments suggests that NDP kinase deficiency stimulates polymerase errors that lead to A:T → G:C transitions and that the editing capacity of cells may be affected, leading to additional uncorrected mispairs and to A:T → T:A transversions.

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