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果蝇的dSmad2和Atr-I传递激活素/转化生长因子β信号。

Drosophila dSmad2 and Atr-I transmit activin/TGFbeta signals.

作者信息

Das P, Inoue H, Baker J C, Beppu H, Kawabata M, Harland R M, Miyazono K, Padgett R W

机构信息

Waksman Institute and Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ 08854-8020, USA.

出版信息

Genes Cells. 1999 Feb;4(2):123-34. doi: 10.1046/j.1365-2443.1999.00244.x.

Abstract

BACKGROUND

Much is known about the three subfamilies of the TGFbeta superfamily in vertebrates-the TGFbetas, dpp/BMPs, and activins. Signalling in each subfamily is dependent on both shared and unique cell surface receptors and Smads. In invertebrates, mutants for BMP pathway components have been extensively characterized, but thus far, evidence for an activin- or TGFbeta-like pathway has been lacking, preventing the use of the extensive genetic tools available for studying several key issues of TGFbeta signalling.

RESULTS

Here we report the identification of dSmad2, a new Drosophila Smad which is most related to the activin/TGFbeta-pathway Smads, Smad2 and Smad3. We show that dSmad2 induces activin responsive genes in Xenopus animal cap assays. dSMAD2 is phosphorylated by ATR-I and PUNT, but not by activated THICK VEINS, and translocates to the nucleus upon activation. Furthermore, we show that dSMAD2 complexes with MEDEA only in the presence of ATR-I and PUNT. dSmad2 is expressed in the imaginal disks and in the outer proliferation centre of the larval brain, suggesting that it may have important proliferative and patterning roles during Drosophila development.

CONCLUSION

Our data provide evidence for the existence of an activin/TGFbeta pathway in Drosophila. We show that dSmad2 participates in this pathway, and that it functions with Atr-I and punt. We show that Medea also participates in this pathway, indicating the conservation of roles for Co-Smads in diverse phyla. Expression patterns of dSmad2 suggest that it functions in imaginal disks and in the brain, in tissues that undergo extensive patterning and proliferation.

摘要

背景

脊椎动物中转化生长因子β(TGFβ)超家族的三个亚家族——TGFβ、dpp/BMP和激活素,人们已经了解很多。每个亚家族中的信号传导都依赖于共享的和独特的细胞表面受体以及Smad蛋白。在无脊椎动物中,BMP信号通路成分的突变体已得到广泛研究,但到目前为止,一直缺乏激活素或TGFβ样信号通路的证据,这使得无法利用现有的大量遗传工具来研究TGFβ信号传导的几个关键问题。

结果

在此,我们报告了果蝇dSmad2的鉴定,它是一种新的果蝇Smad蛋白,与激活素/TGFβ信号通路的Smad蛋白Smad2和Smad3最为相关。我们发现在非洲爪蟾动物帽试验中,dSmad2可诱导激活素反应性基因。dSMAD2可被ATR-I和PUNT磷酸化,但不能被激活的厚脉蛋白磷酸化,激活后可转运至细胞核。此外,我们发现只有在ATR-I和PUNT存在的情况下,dSMAD2才会与MED EA形成复合物。dSmad2在成虫盘和幼虫脑的外增殖中心表达,这表明它可能在果蝇发育过程中具有重要的增殖和模式形成作用。

结论

我们的数据为果蝇中存在激活素/TGFβ信号通路提供了证据。我们表明dSmad2参与了该信号通路,并与Atr-I和punt共同发挥作用。我们还表明MED EA也参与了该信号通路,这表明在不同门中,共-Smad蛋白的作用具有保守性。dSmad2的表达模式表明它在成虫盘和大脑中发挥作用,这些组织会经历广泛的模式形成和增殖。

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