Literature DB >> 8787535

Control and integration of cell signaling pathways during C. elegans vulval development.

M Sundaram1, M Han.   

Abstract

Vulval development in the Caenorhabditis elegans hermaphrodite represents a simple, genetically tractable system for studying how cell signaling events control cell fate decisions. Current models suggest that proper specification of vulval cell fates relies on the integration of multiple signaling systems, including one that involves a receptor tyrosine kinase (RTK)-->Ras-->mitogen activated protein kinase (MAPK) cascade and one that involves a LIN-12/Notch family receptor. In this review, we first discuss how genetic strategies are being used to identify and analyze components that control vulval cell fate decisions. We then describe the different signaling systems that have been elucidated and how they relate to one another. Finally, we highlight several recently characterized genes that encode positive regulators, negative regulators or potential targets of the RTK-->Ras-->MAPK cascade involved in vulval induction.

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Year:  1996        PMID: 8787535     DOI: 10.1002/bies.950180609

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  15 in total

Review 1.  Mitogen-activated protein kinases: specific messages from ubiquitous messengers.

Authors:  H J Schaeffer; M J Weber
Journal:  Mol Cell Biol       Date:  1999-04       Impact factor: 4.272

2.  Ras is required for a limited number of cell fates and not for general proliferation in Caenorhabditis elegans.

Authors:  J Yochem; M Sundaram; M Han
Journal:  Mol Cell Biol       Date:  1997-05       Impact factor: 4.272

3.  Structural requirements for the tissue-specific and tissue-general functions of the Caenorhabditis elegans epidermal growth factor LIN-3.

Authors:  J Liu; P Tzou; R J Hill; P W Sternberg
Journal:  Genetics       Date:  1999-11       Impact factor: 4.562

Review 4.  MAPK signalling: ERK5 versus ERK1/2.

Authors:  Satoko Nishimoto; Eisuke Nishida
Journal:  EMBO Rep       Date:  2006-08       Impact factor: 8.807

5.  Requirements of multiple domains of SLI-1, a Caenorhabditis elegans homologue of c-Cbl, and an inhibitory tyrosine in LET-23 in regulating vulval differentiation.

Authors:  C H Yoon; C Chang; N A Hopper; G M Lesa; P W Sternberg
Journal:  Mol Biol Cell       Date:  2000-11       Impact factor: 4.138

6.  Caenorhabditis elegans lin-25: a study of its role in multiple cell fate specification events involving Ras and the identification and characterization of evolutionarily conserved domains.

Authors:  L Nilsson; T Tiensuu; S Tuck
Journal:  Genetics       Date:  2000-11       Impact factor: 4.562

7.  A Caenorhabditis elegans MAP kinase kinase, MEK-1, is involved in stress responses.

Authors:  M Koga; R Zwaal; K L Guan; L Avery; Y Ohshima
Journal:  EMBO J       Date:  2000-10-02       Impact factor: 11.598

8.  Megakaryocytic differentiation induced by constitutive activation of mitogen-activated protein kinase kinase.

Authors:  A M Whalen; S C Galasinski; P S Shapiro; T S Nahreini; N G Ahn
Journal:  Mol Cell Biol       Date:  1997-04       Impact factor: 4.272

9.  Gain-of-function mutations in the Caenorhabditis elegans lin-1 ETS gene identify a C-terminal regulatory domain phosphorylated by ERK MAP kinase.

Authors:  D Jacobs; G J Beitel; S G Clark; H R Horvitz; K Kornfeld
Journal:  Genetics       Date:  1998-08       Impact factor: 4.562

10.  Split ends antagonizes the Notch and potentiates the EGFR signaling pathways during Drosophila eye development.

Authors:  David B Doroquez; Terry L Orr-Weaver; Ilaria Rebay
Journal:  Mech Dev       Date:  2007-05-21       Impact factor: 1.882

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