dMi-2, a hunchback-interacting protein that functions in Polycomb repression

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....

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Published inScience (American Association for the Advancement of Science) Vol. 282; no. 5395; pp. 1897 - 1900
Main Authors Kehle, J. (University of Bath, Bath, UK.), Beuchle, D, Treuheit, S, Christen, B, Kennison, J.A, Bienz, M, Muller, J
Format Journal Article
LanguageEnglish
Published Washington, DC American Society for the Advancement of Science 04.12.1998
American Association for the Advancement of Science
The American Association for the Advancement of Science
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Summary: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
Bibliography:1999010449
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ISSN:0036-8075
1095-9203
DOI:10.1126/science.282.5395.1897