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Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein.

机译:近端7号染色体上的Peg3印迹基因编码锌指蛋白。

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摘要

Genetic and embryological studies in the mouse demonstrated functional difference between parental chromosomes during development (Surani, M.A.H. et al. 1984, McGrath, J. & Solter, D. 1984). This is due to imprinted genes whose expression is dependenton their parental origin. In our attempt to screen imprinted genes systematically, we have developed a subtraction hybridization methods and have identified 8 paternally expressed genes ,Pegl-8 (Kaneko-Ishino, T. et al. 1985 and in press, Kuroiwa, Y. etd. 1996, Kagitani, F. et al. submitted). The third imprinted genes in our screening named Peg3 (paterndly expressed gene 3) was mapped on proximal chromosome 7 and it is the first imprinted gene identified on this region (Kuroiwa, Y. et al. 1996). It has been demonstrated that maternal disomy of this region causes a neonatal lethality (Searle, A.G. & Beechey, C. V. 1990, Cattanach, B.M. et al. 1992).
机译:在小鼠中进行的遗传和胚胎学研究表明,发育过程中父母染色体之间的功能存在差异(Surani,M.A.H。等,1984; McGrath,J。和Solter,D.1984)。这是由于印迹基因的表达取决于其亲本来源。在我们系统地筛选印迹基因的尝试中,我们开发了一种扣除杂交方法,并鉴定了8个父本表达的基因,Pegl-8(Kaneko-Ishino,T。等人,1985;出版时,Kuroiwa,Y。等人,1996, Kagitani,F.等人提交)。我们筛选中的第三个印迹基因名为Peg3(模式表达的基因3)位于近端7号染色体上,它是在该区域鉴定出的第一个印迹基因(Kuroiwa,Y。等,1996)。已经证明该区域的母亲二体分离引起新生儿致死性(Searle,A.G。&Beechey,C.V.1990,Cattanach,B.M。等人,1992)。

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