Mortazavi Y, Chopra R, Gordon-Smith E C, Rutherford T R
Division of Haematology, St George's Hospital Medical School, London, UK.
J Med Genet. 1997 Dec;34(12):1028-9. doi: 10.1136/jmg.34.12.1028.
X chromosome inactivation is widely studied using DNA sequence polymorphisms and DNA methylation as a surrogate measure of inactivation, but the correlation of methylation with inactivation is not perfect. Thus, it may be better to study sequence polymorphisms expressed in the mRNA. A recent paper reported use of a silent C/T polymorphism at nt 1311 of the G6PD cDNA, and this polymorphism was reported to have a frequency of 40% in all ethnic groups. We have screened 218 English and 50 Iranian subjects by PCR and restriction digestion; 53/218 (24%) British and 22/50 (44%) Iranian subjects were heterozygous. Thus, X inactivation studies using this polymorphism may be useful in some populations, including Iran, but much less so in the UK.
X染色体失活通常利用DNA序列多态性和DNA甲基化作为失活的替代指标进行广泛研究,但甲基化与失活之间的相关性并不完美。因此,研究mRNA中表达的序列多态性可能更好。最近一篇论文报道了在G6PD cDNA第1311位核苷酸处使用沉默的C/T多态性,据报道该多态性在所有种族中的频率为40%。我们通过聚合酶链反应(PCR)和限制性酶切对218名英国人和50名伊朗人进行了筛查;53/218(24%)的英国人和22/50(44%)的伊朗人为杂合子。因此,利用这种多态性进行X失活研究在包括伊朗在内的一些人群中可能有用,但在英国则效果要差得多。