Literature DB >> 7925027

Slow emergence of a multithreshold response to activin requires cell-contact-dependent sharpening but not prepattern.

J B Green1, J C Smith, J C Gerhart.   

Abstract

The growth factor activin elicits mesodermal fates when applied to prospective ectodermal cells of the Xenopus blastula stage embryo. Previous experiments with dissociated cells showed that there are at least five different responses separated by closely spaced, sharp dose thresholds. Here we investigate this multithreshold activin response further using probes for genes expressed at early gastrula stages, namely Xbra, goosecoid, noggin, Xwnt-8 and Mix.1. We show that initial dose-response profiles are broad and smooth in contrast to the later threshold-bound patterns. For Xbra, goosecoid and noggin, the later expression ranges are subsets of earlier ones. Unexpectedly, Xwnt-8 is initially induced at high doses only, but later appears only in cells that have received a low dose of activin. Keeping the cells dissociated after activin treatment, rather than allowing them to reaggregate, prevents sustained expression of Xbra and Xwnt-8 but allows that of goosecoid and noggin. However, cell contact is required for sharpening the dose-response threshold of goosecoid. Finally, we show that a previously reported dorsoventral prepattern in the animal cap is also cell-contact dependent and it is not required for the multi-threshold response to activin.

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Year:  1994        PMID: 7925027     DOI: 10.1242/dev.120.8.2271

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  14 in total

Review 1.  Forming and interpreting gradients in the early Xenopus embryo.

Authors:  James C Smith
Journal:  Cold Spring Harb Perspect Biol       Date:  2009-07       Impact factor: 10.005

2.  Manipulation of gene function in Xenopus laevis.

Authors:  Mizuho S Mimoto; Jan L Christian
Journal:  Methods Mol Biol       Date:  2011

3.  Anteroposterior neural tissue specification by activin-induced mesoderm.

Authors:  J B Green; T L Cook; J C Smith; R M Grainger
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-05       Impact factor: 11.205

Review 4.  Cytosystems dynamics in self-organization of tissue architecture.

Authors:  Yoshiki Sasai
Journal:  Nature       Date:  2013-01-17       Impact factor: 49.962

Review 5.  The transforming growth factor beta family and induction of the vertebrate mesoderm: bone morphogenetic proteins are ventral inducers.

Authors:  R M Harland
Journal:  Proc Natl Acad Sci U S A       Date:  1994-10-25       Impact factor: 11.205

6.  The Xenopus Brachyury promoter is activated by FGF and low concentrations of activin and suppressed by high concentrations of activin and by paired-type homeodomain proteins.

Authors:  B V Latinkić; M Umbhauer; K A Neal; W Lerchner; J C Smith; V Cunliffe
Journal:  Genes Dev       Date:  1997-12-01       Impact factor: 11.361

7.  Jak1 kinase is required for cell migrations and anterior specification in zebrafish embryos.

Authors:  G Conway; A Margoliath; S Wong-Madden; R J Roberts; W Gilbert
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-01       Impact factor: 11.205

8.  Loss of cell adhesion in Xenopus laevis embryos mediated by the cytoplasmic domain of XLerk, an erythropoietin-producing hepatocellular ligand.

Authors:  T L Jones; L D Chong; J Kim; R H Xu; H F Kung; I O Daar
Journal:  Proc Natl Acad Sci U S A       Date:  1998-01-20       Impact factor: 11.205

9.  Establishing positional information through gradient dynamics: a lesson from the Hedgehog signaling pathway.

Authors:  Marcos Nahmad; Angelike Stathopoulos
Journal:  Fly (Austin)       Date:  2010-10-15       Impact factor: 2.160

10.  Embryonic mesoderm cells spread in response to platelet-derived growth factor and signaling by phosphatidylinositol 3-kinase.

Authors:  K Symes; M Mercola
Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-03       Impact factor: 11.205

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