Literature DB >> 2843649

Multiple base-pair mutations in yeast.

D M Hampsey1, J F Ernst, J W Stewart, F Sherman.   

Abstract

The nucleotide changes associated with both forward and reverse mutations at the CYC1 locus in the yeast Saccharomyces cerevisiae have been investigated by sequencing the mutated gene product, iso-1-cytochrome c and, more directly, by sequencing appropriate DNA segments. Although the majority of these mutations are the result of single base-pair changes, approximately 10% are the result of multiple mutations and these occur predominantly at certain sites and with certain patterns. Most multiple base-pair changes occur within 20 nucleotides of each other and are generally within six nucleotides. On the basis of the frequencies and patterns of mutations, these nucleotide changes are considered to have occurred as single, concerted events, rather than as multiple independent mutations. Analysis of these mutations indicates that multiple base-pair changes can arise by widely differing mechanisms. We have recognized the following classes of mutations: multiple base-pair changes that yield (1) direct repeats or (2) inverted repeats of local DNA sequences; (3) substitutions of two tandem base-pairs; (4) frameshift and contiguous single base-pair substitutions; and (5) recombination of the CYC1 gene with a non-allelic gene, resulting in alterations within contiguous segments that can be over 150 nucleotides in length. Some of the multiple base-pair changes do not fall into any of these categories. We suggest mechanisms to account for each of these five classes.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 2843649     DOI: 10.1016/0022-2836(88)90629-8

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


  13 in total

1.  Synonymous substitutions are clustered in enterobacterial genes.

Authors:  A Eyre-Walker
Journal:  J Mol Evol       Date:  1994-11       Impact factor: 2.395

2.  DNA sequence effects on single base deletions arising during DNA polymerization in vitro by Escherichia coli Klenow fragment polymerase.

Authors:  F J Wang; L S Ripley
Journal:  Genetics       Date:  1994-03       Impact factor: 4.562

3.  Enhanced mitochondrial degradation of yeast cytochrome c with amphipathic structures.

Authors:  Xi Chen; Richard P Moerschell; David A Pearce; Durga D Ramanan; Fred Sherman
Journal:  Curr Genet       Date:  2004-12-17       Impact factor: 3.886

4.  SSB recruitment of Exonuclease I aborts template-switching in Escherichia coli.

Authors:  Laura T Laranjo; Stephen J Gross; Danna M Zeiger; Susan T Lovett
Journal:  DNA Repair (Amst)       Date:  2017-06-03

5.  Mutation frequency and specificity with age in liver, bladder and brain of lacI transgenic mice.

Authors:  G R Stuart; Y Oda; J G de Boer; B W Glickman
Journal:  Genetics       Date:  2000-03       Impact factor: 4.562

6.  Frameshift intermediates in homopolymer runs are removed efficiently by yeast mismatch repair proteins.

Authors:  C N Greene; S Jinks-Robertson
Journal:  Mol Cell Biol       Date:  1997-05       Impact factor: 4.272

Review 7.  Template-switching during replication fork repair in bacteria.

Authors:  Susan T Lovett
Journal:  DNA Repair (Amst)       Date:  2017-06-13

8.  DNA sequence analysis of artificially evolved ebg enzyme and ebg repressor genes.

Authors:  B G Hall; P W Betts; J C Wootton
Journal:  Genetics       Date:  1989-12       Impact factor: 4.562

9.  A highly revertible cyc1 mutant of yeast contains a small tandem duplication.

Authors:  G Das; S Consaul; F Sherman
Journal:  Genetics       Date:  1988-09       Impact factor: 4.562

10.  Distinct cis-acting signals enhance 3' endpoint formation of CYC1 mRNA in the yeast Saccharomyces cerevisiae.

Authors:  P Russo; W Z Li; D M Hampsey; K S Zaret; F Sherman
Journal:  EMBO J       Date:  1991-03       Impact factor: 11.598

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.