Eversole-Cire P, Ferguson-Smith A C, Surani M A, Jones P A
Department of Biochemistry and Molecular Biology, USC/Norris Comprehensive Cancer Center, University of Southern California, School of Medicine, Los Angeles 90033, USA.
Cell Growth Differ. 1995 Mar;6(3):337-45.
The insulin-like growth factor 2 (Igf-2) and H19 genes are physically linked on mouse distal chromosome 7 and are reciprocally imprinted. We investigated the molecular basis of the parental imprints in somatic cell cultures derived from normal embryos or from their littermates with maternal uniparental disomy for distal chromosome 7 (MatDi7). In normal cells, the two genes appeared to respond to similar regulatory factor(s), since both genes were coordinately up-regulated upon growth arrest and cell clones which had lost expression of one gene had lost expression of the other. However, in a clone of MatDi7 cells (MatDi7 1-1a), which spontaneously began to express the maternally derived copy of Igf-2, Igf-2 and H19 were not coordinately regulated. MatDi7 1-1a cells showed de novo methylation of sites upstream of Igf-2 and also within the H19 promoter, epigenetic modifications normally seen only on the paternal chromosome. The data provide new experimental evidence for previously hypothesized mechanisms suggesting that Igf-2 and H19 are coordinately regulated.
胰岛素样生长因子2(Igf-2)基因和H19基因在小鼠7号远端染色体上物理相连,并且呈现相互印记。我们研究了源自正常胚胎或其同窝出生的、具有7号远端染色体单亲二体性(MatDi7)的小鼠体细胞培养物中亲本印记的分子基础。在正常细胞中,这两个基因似乎对相似的调控因子起反应,因为在生长停滞时这两个基因都被协同上调,并且失去一个基因表达的细胞克隆也失去了另一个基因的表达。然而,在一个MatDi7细胞克隆(MatDi7 1-1a)中,该克隆自发地开始表达母源的Igf-2拷贝,Igf-2和H19并未受到协同调控。MatDi7 1-1a细胞显示Igf-2上游位点以及H19启动子内出现了从头甲基化,这种表观遗传修饰通常仅见于父本染色体。这些数据为先前假设的Igf-2和H19受协同调控的机制提供了新的实验证据。