THE SPECTRUM OF BETA-THALASSEMIA MUTATIONS IN THE UAE NATIONAL-POPULATION

被引:37
作者
QUAIFE, R
ALGAZALI, L
ABBES, S
FITZGERALD, P
FITCHES, A
VALLER, D
OLD, JM
机构
[1] JOHN RADCLIFFE HOSP,INST MOLEC MED,OXFORD OX3 9DU,ENGLAND
[2] UAE UNIV,FAC MED,DEPT PAEDIAT,AL AIN,U ARAB EMIRATES
[3] UAE UNIV,FAC SCI,DEPT BIOL,AL AIN,U ARAB EMIRATES
[4] AL TAWAM HOSP,DEPT HAEMATOL,AL AIN,U ARAB EMIRATES
关键词
D O I
10.1136/jmg.31.1.59
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The beta thalassaemia alleles in 50 beta thalassaemia heterozygotes originating from many parts of the United Arab Emirates (UAE) have been characterised using the allele specific priming technique of the polymerase chain reaction (PCR). The IVSI-5 (G --> C) mutation was found to be present in 66%, while six other alleles occurred at the much lower frequencies of 2% to 8%. These were codon 8/9 (+G), IVSI-1, 3' end (-25 bp), codon 5 (-CT), IVSII-1 (G --> A), codon 30 (G --> C), and codon 15 (G --> A). The mutation types and percentages are compared with other Mediterranean Arab countries and neighbouring areas. It is proposed that IVSI-5 and other Asian Indian mutations were introduced into the UAE by population migration from the region previously known as Baluchistan. These findings should be useful for genetic counselling and the development of a first trimester prenatal diagnosis programme based on direct detection of mutations in the UAE.
引用
收藏
页码:59 / 61
页数:3
相关论文
共 14 条
[1]  
ALQUOBAILI F, 1993, 5TH P INT C THAL HEM
[2]  
BAYSAL E, 1992, HEMOGLOBIN, V16, P237
[3]  
CHEHAB FF, 1987, BLOOD, V69, P1141
[4]   BETA-THALASSEMIA IN CHINESE - USE OF INVIVO RNA ANALYSIS AND OLIGONUCLEOTIDE HYBRIDIZATION IN SYSTEMATIC CHARACTERIZATION OF MOLECULAR DEFECTS [J].
CHENG, TC ;
ORKIN, SH ;
ANTONARAKIS, SE ;
POTTER, MJ ;
SEXTON, JP ;
MARKHAM, AF ;
GIARDINA, PJV ;
LI, A ;
KAZAZIAN, HH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (09) :2821-2825
[5]  
ELHAZMI MAF, 1991, 4TH INT C THAL HAEM
[6]  
Frye RN, 1961, CENT ASIATIC J, V6, P44
[7]  
KAZAZIAN HH, 1984, EMBO J, V3, P593, DOI 10.1002/j.1460-2075.1984.tb01853.x
[8]   ANALYSIS OF HUMAN Y-CHROMOSOME-SPECIFIC REITERATED DNA IN CHROMOSOME VARIANTS [J].
KUNKEL, LM ;
SMITH, KD ;
BOYER, SH ;
BORGAONKAR, DS ;
WACHTEL, SS ;
MILLER, OJ ;
BREG, WR ;
JONES, HW ;
RARY, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (03) :1245-1249
[9]   MOLECULAR CHARACTERIZATION OF BETA-THALASSEMIA MUTATIONS IN EGYPT [J].
NOVELLETTO, A ;
HAFEZ, M ;
DEIDDA, G ;
DIRIENZO, A ;
FELICETTI, L ;
ELTAHAN, H ;
ELMORSI, Z ;
ELZINY, M ;
ALTONBARY, Y ;
SITTIEN, A ;
TERRENATO, L .
HUMAN GENETICS, 1990, 85 (03) :272-274
[10]   THE SPECTRUM OF BETA-THALASSEMIA MUTATIONS ON THE INDIAN SUBCONTINENT - THE BASIS FOR PRENATAL-DIAGNOSIS [J].
VARAWALLA, NY ;
OLD, JM ;
SARKAR, R ;
VENKATESAN, R ;
WEATHERALL, DJ .
BRITISH JOURNAL OF HAEMATOLOGY, 1991, 78 (02) :242-247