Nibu Y, Zhang H, Levine M
Department of Molecular and Cellular Biology, Division of Genetics, 401 Barker Hall, University of California, Berkeley, CA 94720, USA.
Science. 1998 Apr 3;280(5360):101-4. doi: 10.1126/science.280.5360.101.
Human CtBP attenuates transcriptional activation and tumorigenesis mediated by the adenovirus E1A protein. The E1A sequence motif that interacts with CtBP, Pro-X-Asp-Leu-Ser-X-Lys (P-DLS-K), is present in the repression domains of two unrelated short-range repressors in Drosophila, Knirps and Snail, and is essential for the interaction of these proteins with Drosophila CtBP (dCtBP). A P-element-induced mutation in dCtBP exhibits gene-dosage interactions with a null mutation in knirps, which is consistent with the occurrence of Knirps-dCtBP interactions in vivo. These observations suggest that CtBP and dCtBP are engaged in an evolutionarily conserved mechanism of transcriptional repression, which is used in both Drosophila and mammals.
人类CtBP可减弱腺病毒E1A蛋白介导的转录激活和肿瘤发生。与CtBP相互作用的E1A序列基序Pro-X-Asp-Leu-Ser-X-Lys(P-DLS-K)存在于果蝇中两个不相关的短程阻遏物Knirps和Snail的阻遏结构域中,并且对于这些蛋白质与果蝇CtBP(dCtBP)的相互作用至关重要。dCtBP中的一个P元件诱导突变与knirps中的无效突变表现出基因剂量相互作用,这与体内Knirps-dCtBP相互作用的发生一致。这些观察结果表明,CtBP和dCtBP参与了转录抑制的进化保守机制,该机制在果蝇和哺乳动物中均有应用。