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Title: Isolating human DNA repair genes using rodent-cell mutants

Conference ·
OSTI ID:6645179

The DNA repair systems of rodent and human cells appear to be at least as complex genetically as those in lower eukaryotes and bacteria. The use of mutant lines of rodent cells as a means of identifying human repair genes by functional complementation offers a new approach toward studying the role of repair in mutagenesis and carcinogenesis. In each of six cases examined using hybrid cells, specific human chromosomes have been identified that correct CHO cell mutations affecting repair of damage from uv or ionizing radiations. This finding suggests that both the repair genes and proteins may be virtually interchangeable between rodent and human cells. Using cosmid vectors, human repair genes that map to chromosome 19 have cloned as functional sequences: ERCC2 and XRCC1. ERCC1 was found to have homology with the yeast excision repair gene RAD10. Transformants of repair-deficient cell lines carrying the corresponding human gene show efficient correction of repair capacity by all criteria examined. 39 refs., 1 fig., 1 tab.

Research Organization:
Lawrence Livermore National Lab., CA (USA); Texas Univ., Smithville (USA). Cancer Center
DOE Contract Number:
W-7405-ENG-48
OSTI ID:
6645179
Report Number(s):
UCRL-96478; CONF-8703112-1; ON: DE87008735
Resource Relation:
Conference: Banbury Centre conference on mammalian cell mutagenesis, Cold Springs Harbor, NY, USA, 22 Mar 1987; Other Information: Portions of this document are illegible in microfiche products
Country of Publication:
United States
Language:
English