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胚胎中短程阻遏物与果蝇CtBP的相互作用。

Interaction of short-range repressors with Drosophila CtBP in the embryo.

作者信息

Nibu Y, Zhang H, Levine M

机构信息

Department of Molecular and Cellular Biology, Division of Genetics, 401 Barker Hall, University of California, Berkeley, CA 94720, USA.

出版信息

Science. 1998 Apr 3;280(5360):101-4. doi: 10.1126/science.280.5360.101.

Abstract

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.

摘要

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。

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