Increased frequency of the 2437T allele of the heat shock protein 70-Hom gene in an aged Irish population

被引:36
作者
Ross, OA
Curran, MD
Crum, KA
Rea, IM
Barnett, YA
Middleton, D
机构
[1] Belfast City Hosp, Northern Ireland Reg Histocompatabil & Immunogen, Belfast BT9 7AD, Antrim, North Ireland
[2] Univ Ulster, Sch Biomed Sci, Coleraine BT52 1SA, Londonderry, North Ireland
[3] Queens Univ Belfast, Sch Biol & Biochem, Belfast BT7 1NN, Antrim, North Ireland
[4] Queens Univ Belfast, Dept Geriatr Med, Belfast, Antrim, North Ireland
关键词
heat shock protein; HSP70-Hom; polymorphism and ageing;
D O I
10.1016/S0531-5565(03)00006-8
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The frequency of the functional polymorphism, T2437C transversion (Met --> Thr), in the HSP 70-Hom gene was investigated within a healthy aged Irish population using oligonucleotide probes. The 2437T polymorphic nucleotide was observed to increase in the elderly, although not attaining statistical significance. The TT genotype was observed to be significantly increased within the Irish aged population (p = 0.03), while conversely the TC genotype was significantly decreased in the aged subjects (p = 0.01). These findings would support the theory that the change from a Met (non-polar and hydrophobic) residue to a Thr (polar and neutral) residue may disrupt the peptide-binding specificity of HSP 70-Hom and have an effect on its functional efficiency. One postulates that the highly significant p-value obtained for the TC genotype may infer that the presence of both the T and the C allele (heterozygosity) resulting in the generation of two different HSP 70-Hom protein species may negatively influence longevity. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:561 / 565
页数:5
相关论文
共 32 条
[1]  
Andersen OB, 2000, J GEODESY, V74, P1, DOI 10.1007/s001900050274
[2]  
ARNOLD D, 1995, J EXP MED, V182, P855
[3]   HLA, aging, and longevity:: A critical reappraisal [J].
Caruso, C ;
Candore, G ;
Romano, GC ;
Lio, D ;
Bonafè, M ;
Valensin, S ;
Franceschi, C .
HUMAN IMMUNOLOGY, 2000, 61 (09) :942-949
[4]   Immunogenetics of longevity.: Is major histocompatibility complex polymorphism relevant to the control of human longevity?: A review of literature data [J].
Caruso, C ;
Candore, G ;
Romano, GC ;
Lio, D ;
Bonafè, M ;
Valensin, S ;
Franceschi, C .
MECHANISMS OF AGEING AND DEVELOPMENT, 2001, 122 (05) :445-462
[5]   Long-range PCR amplification as an alternative strategy for characterizing novel HLA-B alleles [J].
Curran, MD ;
Williams, F ;
Earle, JAP ;
Rima, BK ;
vanDam, MG ;
Bunce, M ;
Middleton, D .
EUROPEAN JOURNAL OF IMMUNOGENETICS, 1996, 23 (04) :297-309
[6]  
Favatier F, 1997, CELL STRESS CHAPERON, V2, P141, DOI 10.1379/1466-1268(1997)002<0141:VIHGEA>2.3.CO
[7]  
2
[8]   HSP70 - A MULTIGENE, MULTISTRUCTURE, MULTIFUNCTION FAMILY WITH POTENTIAL CLINICAL-APPLICATIONS [J].
FEIGE, U ;
POLLA, BS .
EXPERIENTIA, 1994, 50 (11-12) :979-986
[9]   Do men and women follow different trajectories to reach extreme longevity? [J].
Franceschi, C ;
Motta, L ;
Valensin, S ;
Rapisarda, R ;
Franzone, A ;
Berardelli, M ;
Motta, M ;
Monti, D ;
Bonafè, M ;
Ferrucci, L ;
Deiana, L ;
Pes, GM ;
Carru, C ;
Desole, MS ;
Barbi, C ;
Sartoni, G ;
Gemelli, C ;
Lescai, F ;
Olivieri, F ;
Marchegiani, F ;
Cardelli, M ;
Cavallone, L ;
Gueresi, P ;
Cossarizza, A ;
Troiano, L ;
Pini, G ;
Sansoni, P ;
Passeri, G ;
Lisa, R ;
Spazzafumo, L ;
Amadio, L ;
Giunta, S ;
Stecconi, R ;
Morresi, R ;
Viticchi, C ;
Mattace, R ;
De Benedictis, G ;
Baggio, G .
AGING-CLINICAL AND EXPERIMENTAL RESEARCH, 2000, 12 (02) :77-84
[10]   GENETIC POLYMORPHISMS OF THE TNFB AND HSP70 GENES LOCATED IN THE HUMAN MAJOR HISTOCOMPATIBILITY COMPLEX IN SARCOIDOSIS [J].
ISHIHARA, M ;
OHNO, S ;
ISHIDA, T ;
MIZUKI, N ;
ANDO, H ;
NARUSE, T ;
ISHIHARA, H ;
INOKO, H .
TISSUE ANTIGENS, 1995, 46 (01) :59-62