Literature DB >> 26096970

Dynamics of Inductive ERK Signaling in the Drosophila Embryo.

Bomyi Lim1, Carmeline J Dsilva2, Thomas J Levario3, Hang Lu3, Trudi Schüpbach4, Ioannis G Kevrekidis5, Stanislav Y Shvartsman6.   

Abstract

Transient activation of the highly conserved extracellular-signal-regulated kinase (ERK) establishes precise patterns of cell fates in developing tissues. Quantitative parameters of these transients are essentially unknown, but a growing number of studies suggest that changes in these parameters can lead to a broad spectrum of developmental abnormalities. We provide a detailed quantitative picture of an ERK-dependent inductive signaling event in the early Drosophila embryo, an experimental system that offers unique opportunities for high-throughput studies of developmental signaling. Our analysis reveals a spatiotemporal pulse of ERK activation that is consistent with a model in which transient production of a short-ranged ligand feeds into a simple signal interpretation system. The pulse of ERK signaling acts as a switch in controlling the expression of the ERK target gene. The quantitative approach that led to this model, based on the integration of data from fixed embryos and live imaging, can be extended to other developmental systems patterned by transient inductive signals.
Copyright © 2015 Elsevier Ltd. All rights reserved.

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Year:  2015        PMID: 26096970      PMCID: PMC4675133          DOI: 10.1016/j.cub.2015.05.039

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  37 in total

1.  corkscrew encodes a putative protein tyrosine phosphatase that functions to transduce the terminal signal from the receptor tyrosine kinase torso.

Authors:  L A Perkins; I Larsen; N Perrimon
Journal:  Cell       Date:  1992-07-24       Impact factor: 41.582

2.  The Drosophila spitz gene encodes a putative EGF-like growth factor involved in dorsal-ventral axis formation and neurogenesis.

Authors:  B J Rutledge; K Zhang; E Bier; Y N Jan; N Perrimon
Journal:  Genes Dev       Date:  1992-08       Impact factor: 11.361

3.  Molecular, phenotypic, and expression analysis of vein, a gene required for growth of the Drosophila wing disc.

Authors:  A A Simcox; G Grumbling; B Schnepp; C Bennington-Mathias; E Hersperger; A Shearn
Journal:  Dev Biol       Date:  1996-08-01       Impact factor: 3.582

4.  In situ activation pattern of Drosophila EGF receptor pathway during development.

Authors:  L Gabay; R Seger; B Z Shilo
Journal:  Science       Date:  1997-08-22       Impact factor: 47.728

5.  rhomboid, a gene required for dorsoventral axis establishment and peripheral nervous system development in Drosophila melanogaster.

Authors:  E Bier; L Y Jan; Y N Jan
Journal:  Genes Dev       Date:  1990-02       Impact factor: 11.361

6.  A group of genes required for pattern formation in the ventral ectoderm of the Drosophila embryo.

Authors:  U Mayer; C Nüsslein-Volhard
Journal:  Genes Dev       Date:  1988-11       Impact factor: 11.361

7.  Establishment of ventral cell fates in the Drosophila embryonic ectoderm requires DER, the EGF receptor homolog.

Authors:  E Raz; B Z Shilo
Journal:  Genes Dev       Date:  1993-10       Impact factor: 11.361

8.  Local apoptosis modulates early mammalian brain development through the elimination of morphogen-producing cells.

Authors:  Keiko Nonomura; Yoshifumi Yamaguchi; Misato Hamachi; Masato Koike; Yasuo Uchiyama; Kenichi Nakazato; Atsushi Mochizuki; Asako Sakaue-Sawano; Atsushi Miyawaki; Hiroki Yoshida; Keisuke Kuida; Masayuki Miura
Journal:  Dev Cell       Date:  2013-12-23       Impact factor: 12.270

Review 9.  The torso pathway in Drosophila: a model system to study receptor tyrosine kinase signal transduction.

Authors:  X Lu; L A Perkins; N Perrimon
Journal:  Dev Suppl       Date:  1993

10.  The dorsal gradient morphogen regulates stripes of rhomboid expression in the presumptive neuroectoderm of the Drosophila embryo.

Authors:  Y T Ip; R E Park; D Kosman; E Bier; M Levine
Journal:  Genes Dev       Date:  1992-09       Impact factor: 11.361

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  25 in total

Review 1.  Cell signaling regulation by protein phosphorylation: a multivariate, heterogeneous, and context-dependent process.

Authors:  Evan K Day; Nisha G Sosale; Matthew J Lazzara
Journal:  Curr Opin Biotechnol       Date:  2016-07-06       Impact factor: 9.740

2.  Co-culture Activation of MAP Kinase in Drosophila S2 Cells.

Authors:  Josefa Steinhauer
Journal:  Methods Mol Biol       Date:  2017

3.  Functional divergence caused by mutations in an energetic hotspot in ERK2.

Authors:  Clinton A Taylor; Kevin W Cormier; Shannon E Keenan; Svetlana Earnest; Steve Stippec; Chonlarat Wichaidit; Yu-Chi Juang; Junmei Wang; Stanislav Y Shvartsman; Elizabeth J Goldsmith; Melanie H Cobb
Journal:  Proc Natl Acad Sci U S A       Date:  2019-07-11       Impact factor: 11.205

Review 4.  New Twists in Drosophila Cell Signaling.

Authors:  Ben-Zion Shilo
Journal:  J Biol Chem       Date:  2016-02-23       Impact factor: 5.157

5.  A Real-Time Biosensor for ERK Activity Reveals Signaling Dynamics during C. elegans Cell Fate Specification.

Authors:  Claire de la Cova; Robert Townley; Sergi Regot; Iva Greenwald
Journal:  Dev Cell       Date:  2017-08-17       Impact factor: 12.270

6.  Optogenetic Rescue of a Patterning Mutant.

Authors:  Heath E Johnson; Nareg J V Djabrayan; Stanislav Y Shvartsman; Jared E Toettcher
Journal:  Curr Biol       Date:  2020-07-23       Impact factor: 10.834

Review 7.  The Role of Peptide Hormones in Insect Lipid Metabolism.

Authors:  Umut Toprak
Journal:  Front Physiol       Date:  2020-05-07       Impact factor: 4.566

8.  Divergent effects of intrinsically active MEK variants on developmental Ras signaling.

Authors:  Yogesh Goyal; Granton A Jindal; José L Pelliccia; Kei Yamaya; Eyan Yeung; Alan S Futran; Rebecca D Burdine; Trudi Schüpbach; Stanislav Y Shvartsman
Journal:  Nat Genet       Date:  2017-02-06       Impact factor: 38.330

9.  A Transport Model for Estimating the Time Course of ERK Activation in the C. elegans Germline.

Authors:  Henry H Mattingly; Jessica J Chen; Swathi Arur; Stanislav Y Shvartsman
Journal:  Biophys J       Date:  2015-12-01       Impact factor: 4.033

10.  Rapid Dynamics of Signal-Dependent Transcriptional Repression by Capicua.

Authors:  Shannon E Keenan; Shelby A Blythe; Robert A Marmion; Nareg J-V Djabrayan; Eric F Wieschaus; Stanislav Y Shvartsman
Journal:  Dev Cell       Date:  2020-03-05       Impact factor: 12.270

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