Literature DB >> 10887086

Dpp signaling thresholds in the dorsal ectoderm of the Drosophila embryo.

H L Ashe1, M Mannervik, M Levine.   

Abstract

The dorsal ectoderm of the Drosophila embryo is subdivided into different cell types by an activity gradient of two TGF(&bgr;) signaling molecules, Decapentaplegic (Dpp) and Screw (Scw). Patterning responses to this gradient depend on a secreted inhibitor, Short gastrulation (Sog) and a newly identified transcriptional repressor, Brinker (Brk), which are expressed in neurogenic regions that abut the dorsal ectoderm. Here we examine the expression of a number of Dpp target genes in transgenic embryos that contain ectopic stripes of Dpp, Sog and Brk expression. These studies suggest that the Dpp/Scw activity gradient directly specifies at least three distinct thresholds of gene expression in the dorsal ectoderm of gastrulating embryos. Brk was found to repress two target genes, tailup and pannier, that exhibit different limits of expression within the dorsal ectoderm. These results suggest that the Sog inhibitor and Brk repressor work in concert to establish sharp dorsolateral limits of gene expression. We also present evidence that the activation of Dpp/Scw target genes depends on the Drosophila homolog of the CBP histone acetyltransferase.

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Year:  2000        PMID: 10887086     DOI: 10.1242/dev.127.15.3305

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


  37 in total

1.  Brinker is a sequence-specific transcriptional repressor in the Drosophila embryo.

Authors:  H Zhang; M Levine; H L Ashe
Journal:  Genes Dev       Date:  2001-02-01       Impact factor: 11.361

2.  An analysis using the hobo genetic system reveals that combinatorial signaling by the Dpp and Wg pathways regulates dpp expression in leading edge cells of the dorsal ectoderm in Drosophila melanogaster.

Authors:  S J Newfeld; N T Takaesu
Journal:  Genetics       Date:  2002-06       Impact factor: 4.562

3.  Facilitated transport of a Dpp/Scw heterodimer by Sog/Tsg leads to robust patterning of the Drosophila blastoderm embryo.

Authors:  Osamu Shimmi; David Umulis; Hans Othmer; Michael B O'Connor
Journal:  Cell       Date:  2005-03-25       Impact factor: 41.582

4.  Genetic regulation of patterned tubular branching in Drosophila.

Authors:  E Hatton-Ellis; C Ainsworth; Y Sushama; S Wan; K VijayRaghavan; H Skaer
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-26       Impact factor: 11.205

Review 5.  Nuclear interpretation of Dpp signaling in Drosophila.

Authors:  M Affolter; T Marty; M A Vigano; A Jaźwińska
Journal:  EMBO J       Date:  2001-07-02       Impact factor: 11.598

6.  A Developmental Program Truncates Long Transcripts to Temporally Regulate Cell Signaling.

Authors:  Jeremy E Sandler; Jihyun Irizarry; Vincent Stepanik; Leslie Dunipace; Henry Amrhein; Angelike Stathopoulos
Journal:  Dev Cell       Date:  2018-12-17       Impact factor: 12.270

Review 7.  Generation of extracellular morphogen gradients: the case for diffusion.

Authors:  Kristina S Stapornwongkul; Jean-Paul Vincent
Journal:  Nat Rev Genet       Date:  2021-03-25       Impact factor: 53.242

8.  Transcriptional regulation of the Drosophila gene zen by competing Smad and Brinker inputs.

Authors:  C Rushlow; P F Colosimo; M C Lin; M Xu; N Kirov
Journal:  Genes Dev       Date:  2001-02-01       Impact factor: 11.361

9.  A genetic screen identifies putative targets and binding partners of CREB-binding protein in the developing Drosophila eye.

Authors:  Jason Anderson; Rohan Bhandari; Justin P Kumar
Journal:  Genetics       Date:  2005-07-05       Impact factor: 4.562

10.  Multistep molecular mechanism for bone morphogenetic protein extracellular transport in the Drosophila embryo.

Authors:  Annick Sawala; Catherine Sutcliffe; Hilary L Ashe
Journal:  Proc Natl Acad Sci U S A       Date:  2012-06-25       Impact factor: 11.205

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