Pohlenz J, Schönberger W, Wemme H, Winterpacht A, Wirth S, Zabel B
Children's Hospital of the Johannes-Gutenberg-University, Mainz, Germany.
Hum Mutat. 1996;7(1):79-81. doi: 10.1002/(SICI)1098-1004(1996)7:1<79::AID-HUMU15>3.0.CO;2-P.
Two years after the first mutation on exon 7 in the carboxy-terminal part of the hinge domain (D) was reported (Behr and Loos 1992), we have identified the second mutation on exon 7 in patients with GRTH. Interestingly, our mutation it is not located in the two previously described "hot spot regions", but instead very close to the hinge domain (D) of the receptor protein that is essential for the function of the hormone binding domain (E) (Lin et al., 1991). Confirming the observation that the majority of single base substitutions causing human genetic diseases or DNA polymorphisms follow the hot spot mutation rule of CG to TG and CG to CA transition (Barker et al., 1984), an additional CpG dinucleotide transition has been identified.
在铰链结构域(D)羧基末端外显子7上首次发现突变(Behr和Loos,1992年)两年后,我们在GRTH患者中鉴定出了外显子7上的第二个突变。有趣的是,我们发现的突变并不位于之前描述的两个“热点区域”,而是非常靠近受体蛋白的铰链结构域(D),而铰链结构域(D)对激素结合结构域(E)的功能至关重要(Lin等人,1991年)。大多数导致人类遗传疾病或DNA多态性的单碱基替换遵循CG到TG和CG到CA转换的热点突变规则(Barker等人,1984年),这一观察结果得到了证实,我们还发现了另外一个CpG二核苷酸转换。