Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1995 Aug;140(4):1199-211.
doi: 10.1093/genetics/140.4.1199.

The role of DNA repair genes in recombination between repeated sequences in yeast

Affiliations

The role of DNA repair genes in recombination between repeated sequences in yeast

B Liefshitz et al. Genetics. 1995 Aug.

Abstract

The presence of repeated sequences in the genome represents a potential source of karyotypic instability. Genetic control of recombination is thus important to preserve the integrity of the genome. To investigate the genetic control of recombination between repeated sequences, we have created a series of isogenic strains in which we could assess the role of genes involved in DNA repair in two types of recombination: direct repeat recombination and ectopic gene conversion. Naturally occurring (Ty elements) and artificially constructed repeats could be compared in the same cell population. We have found that direct repeat recombination and gene conversion have different genetic requirements. The role of the RAD51, RAD52, RAD54, RAD55, and RAD57 genes, which are involved in recombinational repair, was investigated. Based on the phenotypes of single and double mutants, these genes can be divided into three functional subgroups: one composed of RAD52, a second one composed of RAD51 and RAD54, and a third one that includes the RAD55 and RAD57 genes. Among seven genes involved in excision repair tested, only RAD1 and RAD10 played a role in the types of recombination studied. We did not detect a differential effect of any rad mutation on Ty elements as compared to artificially constructed repeats.

PubMed Disclaimer

References

    1. Genetics. 1989 Dec;123(4):683-94 - PubMed
    1. Nature. 1981 Jul 23;292(5821):306-11 - PubMed
    1. Nature. 1992 Feb 6;355(6360):555-8 - PubMed
    1. Genetics. 1988 Oct;120(2):367-77 - PubMed
    1. Genetics. 1995 Jan;139(1):109-23 - PubMed

Publication types

MeSH terms