Webb T, Whittington J, Holland A J, Soni S, Boer H, Clarke D, Horsthemke B
Section of Medical and Molecular Genetics, University of Birmingham, Birmingham, UK.
Clin Genet. 2006 Jan;69(1):26-32. doi: 10.1111/j.1399-0004.2006.00536.x.
Although Prader-Willi syndrome (PWS) has been linked to the loss of function of imprinted genes in 15q11q13, very little is known about the pathogenesis. Using quantitative real-time PCR, we have confirmed the previous observation of an abnormality of CD36 expression in cells with maternal uniparental disomy 15, obtained from a proband with mosaicism for PWS, by demonstrating reduced expression levels in blood cells from a series of non-mosaic probands with PWS. Furthermore, we have extended these observations to show that CD36 expression in a non-PWS population is inversely correlated with body mass index but that this correlation does not hold in PWS. CD36 which maps to 7q11.2 is the first gene outside the 15q11q13 region whose level of expression appears to be reduced in people with PWS. Low CD36 expression levels in PWS point to an abnormal control of lipid and glucose homeostasis which may explain the insatiable hunger in these patients.
尽管普拉德-威利综合征(PWS)与15q11q13区域印记基因功能丧失有关,但对其发病机制却知之甚少。通过定量实时PCR,我们证实了先前的观察结果,即从一名PWS嵌合体先证者获得的母源单亲二体15细胞中CD36表达异常,方法是通过检测一系列非嵌合PWS先证者血细胞中CD36表达水平降低。此外,我们进一步扩展了这些观察结果,发现非PWS人群中CD36表达与体重指数呈负相关,但在PWS患者中这种相关性并不成立。定位于7q11.2的CD36是15q11q13区域外第一个在PWS患者中表达水平似乎降低的基因。PWS患者中CD36低表达表明脂质和葡萄糖稳态控制异常,这可能解释了这些患者难以满足的饥饿感。