Literature DB >> 9076683

The C-terminal domain of Mad-like signal transducers is sufficient for biological activity in the Xenopus embryo and transcriptional activation.

G Meersseman1, K Verschueren, L Nelles, C Blumenstock, H Kraft, G Wuytens, J Remacle, C A Kozak, P Tylzanowski, C Niehrs, D Huylebroeck.   

Abstract

We report the characterization of two vertebrate homologs of Drosophila mothers against dpp (Mad) isolated from the mouse and the Xenopus embryo, named MusMLP (mad-like protein) and XenMLP, respectively, together with a summary of their expression patterns in the embryo. Overexpression of XenMLP causes ventralization of Xenopus embryos and we demonstrate that the C-terminal domain is necessary and sufficient to confer this biological effect. This domain also has the potential for transcriptional activation, as shown in one-hybrid assays in mammalian cells. We further demonstrate that MLPs are multidomain proteins by showing a cis-negative effect of the N-terminal domain on the transactivation by the C-terminal domain and that the proline-rich, middle domain maximizes the activity of the C-terminal domain. We also mapped the MusMLP gene to a region on mouse chromosome 13 that corresponds to a region on human chromosome 5q that contains cancer-related genes.

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Year:  1997        PMID: 9076683     DOI: 10.1016/s0925-4773(96)00629-6

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  9 in total

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2.  Tel, a frequent target of leukemic translocations, induces cellular aggregation and influences expression of extracellular matrix components.

Authors:  L Van Rompaey; W Dou; A Buijs; G Grosveld
Journal:  Neoplasia       Date:  1999-12       Impact factor: 5.715

3.  Smad proteins exist as monomers in vivo and undergo homo- and hetero-oligomerization upon activation by serine/threonine kinase receptors.

Authors:  M Kawabata; H Inoue; A Hanyu; T Imamura; K Miyazono
Journal:  EMBO J       Date:  1998-07-15       Impact factor: 11.598

4.  TGF-beta receptor-mediated signalling through Smad2, Smad3 and Smad4.

Authors:  A Nakao; T Imamura; S Souchelnytskyi; M Kawabata; A Ishisaki; E Oeda; K Tamaki; J Hanai; C H Heldin; K Miyazono; P ten Dijke
Journal:  EMBO J       Date:  1997-09-01       Impact factor: 11.598

5.  Direct binding of Smad3 and Smad4 to critical TGF beta-inducible elements in the promoter of human plasminogen activator inhibitor-type 1 gene.

Authors:  S Dennler; S Itoh; D Vivien; P ten Dijke; S Huet; J M Gauthier
Journal:  EMBO J       Date:  1998-06-01       Impact factor: 11.598

6.  XSmad2 directly activates the activin-inducible, dorsal mesoderm gene XFKH1 in Xenopus embryos.

Authors:  M Howell; C S Hill
Journal:  EMBO J       Date:  1997-12-15       Impact factor: 11.598

7.  Dose-dependent Smad1, Smad5 and Smad8 signaling in the early mouse embryo.

Authors:  Sebastian J Arnold; Silvia Maretto; Ayesha Islam; Elizabeth K Bikoff; Elizabeth J Robertson
Journal:  Dev Biol       Date:  2006-08-01       Impact factor: 3.582

8.  Xvent-1 mediates BMP-4-induced suppression of the dorsal-lip-specific early response gene XFD-1' in Xenopus embryos.

Authors:  H Friedle; S Rastegar; H Paul; E Kaufmann; W Knöchel
Journal:  EMBO J       Date:  1998-04-15       Impact factor: 11.598

9.  Neotendon formation induced by manipulation of the Smad8 signalling pathway in mesenchymal stem cells.

Authors:  Andrea Hoffmann; Gadi Pelled; Gadi Turgeman; Peter Eberle; Yoram Zilberman; Hadassah Shinar; Keren Keinan-Adamsky; Andreas Winkel; Sandra Shahab; Gil Navon; Gerhard Gross; Dan Gazit
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  9 in total

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