Quantcast
Environmental Health Perspectives Free Trail Issue
Author Keyword Title Full
About EHP Publications Past Issues News By Topic Authors Subscribe Press International Inside EHP Email Alerts spacer
Environmental Health Perspectives (EHP) is a monthly journal of peer-reviewed research and news on the impact of the environment on human health. EHP is published by the National Institute of Environmental Health Sciences and its content is free online. Print issues are available by paid subscription.DISCLAIMER
spacer
NIEHS
NIH
DHHS
spacer
Current Issue

EHP Science Education Website




Comparative Toxicogenomics Database (CTD)

spacer
Environmental Health Perspectives Volume 111, Number 15, November 2003 Open Access
spacer
Functional Characterization of Polymorphisms in DNA Repair Genes Using Cytogenetic Challenge Assays

William W. Au,1 Salama A. Salama,1,* and Carlos H. Sierra-Torres2

1Department of Preventive Medicine and Community Health, The University of Texas Medical Branch, Galveston, Texas, USA; 2Laboratorio de Genética Humana, Departamento de Ciencas Fisiológicas, Universidad del Cauca, Popáyan, Colombia

Abstract
A major barrier to understanding the role of polymorphic DNA repair genes for environmental cancer is that the functions of variant genotypes are largely unknown. Using our cytogenetic challenge assays, we conducted an investigation to address the deficiency. Using X-rays or ultraviolet (UV) light, we irradiated blood lymphocytes from 80 nonsmoking donors to challenge the cells to repair the induced DNA damage, and we analyzed expression of chromosome aberrations (CA) specific to the inducing agents. We have genotyped polymorphic DNA repair genes preferentially involved with base excision repair (BER) and nucleotide excision repair (NER) activities (XRCC1, XRCC3, APE1, XPD) corresponding to the repair of X-ray- and UV light-induced DNA damage, respectively. We expected that defects in specific DNA repair pathways due to polymorphisms would cause corresponding increases of specific CA. From our data, XRCC1 399Gln and XRCC3 241Met were associated with significant increases in chromosome deletions compared with the corresponding homozygous wild types (18.27 ± 1.1 vs 14.79 ± 1.2 and 18.22 ± 0.99 vs 14.20 ± 1.39, respectively) ; XPD 312Asn and XPD 751Gln were associated with significant increases in chromatid breaks compared with wild types (16.09 ± 1.36 vs 11.41 ± 0.98 and 16.87 ± 1.27 vs 10.54 ± 0.87, respectively) , p < 0.05. The data indicate that XRCC1 399Gln and XRCC3 241Met are significantly defective in BER, and the XPD 312Asn and XPD 751Gln are significantly defective in NER. In addition, the variant genotypes interact significantly, with limited overlap of the two different repair pathways. Key words: , , , , , . Environ Health Perspect 111:1843-1850 (2003) . doi:10.1289/txg.6632 available via http://dx.doi.org/ [Online 6 October 2003]


The full version of this article is available for free in HTML or PDF formats.
spacer
 
Open Access Resources | Call for Papers | Career Opportunities | Buy EHP Publications | Advertising Information | Subscribe to the EHP News Feeds News Feeds | Inspector General USA.gov