Lerer I, Sagi M, Cutting G R, Abeliovich D
Department of Human Genetics, Hadassah Hebrew University Hospital, Jerusalem, Israel.
J Med Genet. 1992 Feb;29(2):131-3. doi: 10.1136/jmg.29.2.131.
We have screened our CF patients for mutations in exons 10 and 11 of the CFTR gene. Two mutations, delta F508 and G542X, have been found in 66 Jewish CF patients. The average frequency of the delta F508 mutation in the Jewish population is 33.8%. The G542X mutation accounts for 13% of the Ashkenazi CF mutations and has been found in three out of seven chromosomes of Jewish patients from Turkey (probably descended from Ashkenazi immigrants). The G542X mutation was not found in any of the other non-Ashkenazi patients. All the G542X bearing chromosomes have the same haplotype. Based on these observations it is concluded that the G542X mutation was introduced into the Jewish people after the split into Ashkenazi and non-Ashkenazi.
我们对囊性纤维化(CF)患者的囊性纤维化跨膜传导调节因子(CFTR)基因第10和11外显子的突变情况进行了筛查。在66名犹太裔CF患者中发现了两种突变,即ΔF508和G542X。犹太人群中ΔF508突变的平均频率为33.8%。G542X突变占阿什肯纳兹犹太人CF突变的13%,在来自土耳其的犹太患者的七条染色体中有三条发现了该突变(可能源自阿什肯纳兹移民)。在其他非阿什肯纳兹患者中均未发现G542X突变。所有携带G542X的染色体都具有相同的单倍型。基于这些观察结果得出结论,G542X突变是在犹太人群分裂为阿什肯纳兹和非阿什肯纳兹之后才引入的。