Kehle J, Beuchle D, Treuheit S, Christen B, Kennison J A, Bienz M, Müller J
Max-Planck-Institut für Entwicklungsbiologie, Spemannstrasse 35/III, 72076 Tübingen, Germany.
Science. 1998 Dec 4;282(5395):1897-900. doi: 10.1126/science.282.5395.1897.
Early in Drosophila embryogenesis, gap gene products directly repress transcription of homeotic (HOX) genes and thereby delimit HOX expression domains. Subsequently, Polycomb-group proteins maintain this repression. Currently, there is no known molecular link between gap and Polycomb-group proteins. Here, dMi-2 is identified as a protein that binds to a domain in the gap protein Hunchback that is specifically required for the repression of HOX genes. Genetic analyses show that dMi-2 participates in both Hunchback and Polycomb repression in vivo. Hence, recruitment of dMi-2 may serve as a link between repression of HOX genes by Hunchback and Polycomb proteins.
在果蝇胚胎发育早期,间隙基因产物直接抑制同源异型(HOX)基因的转录,从而界定HOX基因的表达域。随后,多梳蛋白家族维持这种抑制作用。目前,间隙蛋白和多梳蛋白家族成员之间尚未发现已知的分子联系。在这里,dMi-2被鉴定为一种与间隙蛋白驼背中一个结构域结合的蛋白质,该结构域是抑制HOX基因所特需的。遗传学分析表明,dMi-2在体内参与驼背蛋白和多梳蛋白介导的基因抑制。因此,dMi-2的募集可能在驼背蛋白和多梳蛋白对HOX基因的抑制之间起到联系作用。