Microheterogeneity in the distribution of the 844ins68 in the cystathionine β-synthase gene in Italy

被引:14
作者
Giusti, B
Camacho-Vanegas, O
Attanasio, M
Comeglio, P
Gori, AM
Brunelli, T
Prisco, D
Gensini, GF
Abbate, R
Pepe, G
机构
[1] Univ Florence, Ist Clin Med Gen & Cardiol, I-50134 Florence, Italy
[2] Univ Roma Tor Vergata, Dipartimento Biol, I-00173 Rome, Italy
关键词
cystathionine beta-synthase; anthropological DNA marker; microheterogeneity;
D O I
10.1016/S0049-3848(99)00005-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cystathionine beta-synthase (CBS) is an important enzyme for methionine metabolism. A common 844ins68 insertion variant in the CBS gene has been described. This 68-bp duplication of the intron 7-exon 8 boundary within the CBS gene already has been reported to be associated in cis with the T833C mutation. Heterozygosity for CBS deficiency is considered an important cause of hyperhomocysteinemia that strongly relates to cardiovascular disease, as well as homozygosity for another common variant, the C677T mutation of 5,10-methylene tetrahydrofolate reductase. We analysed the prevalence of the 844ins68 variant in the CBS gene in 595 unrelated apparently healthy individuals from nine Italian regions and in 133 patients with coronary artery disease. Our data confirm that the T833C mutation cosegregates in cis with the 844ins68 in all carriers of the insertion. Furthermore, no statistical difference was found in the insertion variant allele frequency between controls and coronary artery disease patients. Our study indicates a microheterogeneity in the distribution of the 844ins68 in the Italian population. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:249 / 254
页数:6
相关论文
共 19 条
[1]  
Abbate R, 1998, THROMB HAEMOSTASIS, V79, P727
[2]  
Boers GHJ, 1997, THROMB HAEMOSTASIS, V78, P520
[3]  
Botto LD, 1998, CLIN GENET, V53, P456
[4]   HYPERHOMOCYSTEINEMIA - AN INDEPENDENT RISK FACTOR FOR VASCULAR-DISEASE [J].
CLARKE, R ;
DALY, L ;
ROBINSON, K ;
NAUGHTEN, E ;
CAHALANE, S ;
FOWLER, B ;
GRAHAM, I .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (17) :1149-1155
[5]   A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE [J].
FROSST, P ;
BLOM, HJ ;
MILOS, R ;
GOYETTE, P ;
SHEPPARD, CA ;
MATTHEWS, RG ;
BOERS, GJH ;
DENHEIJER, M ;
KLUIJTMANS, LAJ ;
VANDENHEUVEL, LP ;
ROZEN, R .
NATURE GENETICS, 1995, 10 (01) :111-113
[6]  
Giusti B, 1997, THROMB HAEMOSTASIS, V78, P1293
[7]   Plasma homocysteine as a risk factor for vascular disease - The European concerted action project [J].
Graham, IM ;
Daly, LE ;
Refsum, HM ;
Robinson, K ;
Brattstrom, LE ;
Ueland, PM ;
PalmaReis, RJ ;
Boers, GHJ ;
Sheahan, RG ;
Israelsson, B ;
Uiterwaal, CS ;
Meleady, R ;
McMaster, D ;
Verhoef, P ;
Witteman, J ;
Rubba, P ;
Bellet, H ;
Wautrecht, JC ;
deValk, HW ;
Luis, ACS ;
ParrotRoulaud, FM ;
Tan, KS ;
Higgins, I ;
Garcon, D ;
Medrano, MJ ;
Candito, M ;
Evans, AE ;
Andria, G .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (22) :1775-1781
[8]   2 NOVEL MISSENSE MUTATIONS IN THE CYSTATHIONINE BETA-SYNTHASE GENE IN HOMOCYSTINURIC PATIENTS [J].
KLUIJTMANS, LAJ ;
BLOM, HJ ;
BOERS, GHJ ;
VANOOST, BA ;
TRIJBELS, FJM ;
VANDENHEUVEL, LPWJ .
HUMAN GENETICS, 1995, 96 (02) :249-250
[9]   A common 844INS68 insertion variant in the cystathionine beta-synthase gene [J].
Kluijtmans, LAJ ;
Boers, GHJ ;
Trijbels, FJM ;
vanLithZanders, HMA ;
vandenHeuvel, LPWJ ;
Blom, HJ .
BIOCHEMICAL AND MOLECULAR MEDICINE, 1997, 62 (01) :23-25
[10]  
Kozich Viktor, 1992, Human Mutation, V1, P113, DOI 10.1002/humu.1380010206