Impact of ERCC2 gene polymorphism on HIV-1 disease progression to AIDS among North Indian HIV patients

被引:2
作者
Sobti, Ranbir Chander [1 ]
Berhane, Nega [1 ]
Mahdi, Salih Abdul [1 ]
Kler, Rupinder [1 ]
Hosseini, Seyed Ali [1 ]
Kuttiat, Vijish [2 ]
Wanchu, Ajay [2 ]
机构
[1] Panjab Univ, Dept Biotechnol, Chandigarh 160014, India
[2] Postgrad Inst Med Educ & Res, Dept Internal Med, Chandigarh 160012, India
关键词
ERCC2; polymorphism; Disease progression; HIV; 1; CHEMOKINE RECEPTOR GENE; DNA-REPAIR GENES; XPD POLYMORPHISMS; BREAST-CANCER; EXCISION-REPAIR; VIRAL PHENOTYPE; INFECTION; RISK; CCR5; INDIVIDUALS;
D O I
10.1007/s11033-010-9958-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
HIV/AIDS remains to be one of the killing diseases of mankind. Host genetic response is one of the factor which determine susceptibility to HIV and disease progression to AIDS. The aim of the present study was to evaluate the impact of ERCC2 Lyc (751) Gln (excision repair cross complementing rodent repair deficiency, complementation group 2) polymorphism on HIV-1 susceptibility and disease progression to AIDS, as this gene has been reported to intervene in degrading retroviral cDNA before it integrates with the host DNA. This case control study included 300 HIV seropositive cases and an equal number of HIV seronegative controls. DNA was isolated from the blood samples of study subjects and genotyping of ERCC2 was conducted by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) method. The Gln/Gln genotype showed a significant variation between cases and controls (P = 0.047, OR 1.71, 95% CI 1.00-2.93), indicating a possible role of susceptibility in reference to controls and disease progression when compared within cases.
引用
收藏
页码:2945 / 2952
页数:8
相关论文
共 44 条
[41]   Nucleotide excision repair gene XPD polymorphisms and genetic predisposition to melanoma [J].
Tomescu, D ;
Kavanagh, G ;
Ha, T ;
Campbell, H ;
Melton, DW .
CARCINOGENESIS, 2001, 22 (03) :403-408
[42]   The XPB and XPD DNA helicases are components of the p53-mediated apoptosis pathway [J].
Wang, XW ;
Vermeulen, W ;
Coursen, JD ;
Gibson, M ;
Lupold, SE ;
Forrester, K ;
Xu, GW ;
Elmore, L ;
Yeh, H ;
Hoeijmakers, JHJ ;
Harris, CC .
GENES & DEVELOPMENT, 1996, 10 (10) :1219-1232
[43]   The DNA repair genes XPB and XPD defend cells from retroviral infection [J].
Yoder, K ;
Sarasin, A ;
Kraemer, K ;
McIlhatton, M ;
Bushman, F ;
Fishel, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (12) :4622-4627
[44]  
UNAIDS0827EJC1511E