Literature DB >> 20108317

Cell fate specification in the C. elegans embryo.

Morris F Maduro1.   

Abstract

Cell specification requires that particular subsets of cells adopt unique expression patterns that ultimately define the fates of their descendants. In C. elegans, cell fate specification involves the combinatorial action of multiple signals that produce activation of a small number of "blastomere specification" factors. These initiate expression of gene regulatory networks that drive development forward, leading to activation of "tissue specification" factors. In this review, the C. elegans embryo is considered as a model system for studies of cell specification. The techniques used to study cell fate in this species, and the themes that have emerged, are described. Copyright (c) 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20108317     DOI: 10.1002/dvdy.22233

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  23 in total

1.  The C. elegans embryonic fate specification factor EGL-18 (GATA) is reutilized downstream of Wnt signaling to maintain a population of larval progenitor cells.

Authors:  Lakshmi Gorrepati; David M Eisenmann
Journal:  Worm       Date:  2015-01-27

2.  Future translational applications from the contemporary genomics era: a scientific statement from the American Heart Association.

Authors:  Caroline S Fox; Jennifer L Hall; Donna K Arnett; Euan A Ashley; Christian Delles; Mary B Engler; Mason W Freeman; Julie A Johnson; David E Lanfear; Stephen B Liggett; Aldons J Lusis; Joseph Loscalzo; Calum A MacRae; Kiran Musunuru; L Kristin Newby; Christopher J O'Donnell; Stephen S Rich; Andre Terzic
Journal:  Circulation       Date:  2015-04-16       Impact factor: 29.690

Review 3.  Programmed and self-organized flow of information during morphogenesis.

Authors:  Claudio Collinet; Thomas Lecuit
Journal:  Nat Rev Mol Cell Biol       Date:  2021-01-22       Impact factor: 94.444

4.  Reciprocal signaling by Wnt and Notch specifies a muscle precursor in the C. elegans embryo.

Authors:  Scott M Robertson; Jessica Medina; Marieke Oldenbroek; Rueyling Lin
Journal:  Development       Date:  2017-01-03       Impact factor: 6.868

5.  Development of blastomere clones in the Ilyanassa embryo: transformation of the spiralian blastula into the larval body plan.

Authors:  Xin Yi Chan; J David Lambert
Journal:  Dev Genes Evol       Date:  2014-06-08       Impact factor: 0.900

6.  Quantitating transcription factor redundancy: The relative roles of the ELT-2 and ELT-7 GATA factors in the C. elegans endoderm.

Authors:  Aidan Dineen; Erin Osborne Nishimura; Barbara Goszczynski; Joel H Rothman; James D McGhee
Journal:  Dev Biol       Date:  2018-01-31       Impact factor: 3.582

7.  A 4D single-cell protein atlas of transcription factors delineates spatiotemporal patterning during embryogenesis.

Authors:  Xuehua Ma; Zhiguang Zhao; Long Xiao; Weina Xu; Yahui Kou; Yanping Zhang; Gang Wu; Yangyang Wang; Zhuo Du
Journal:  Nat Methods       Date:  2021-07-26       Impact factor: 28.547

Review 8.  Going with the flow: insights from Caenorhabditis elegans zygote polarization.

Authors:  Alicia G Gubieda; John R Packer; Iolo Squires; Jack Martin; Josana Rodriguez
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2020-08-24       Impact factor: 6.237

9.  The onset of C. elegans dosage compensation is linked to the loss of developmental plasticity.

Authors:  Laura M Custer; Martha J Snyder; Kerry Flegel; Györgyi Csankovszki
Journal:  Dev Biol       Date:  2013-11-16       Impact factor: 3.582

10.  MRCK-1 Drives Apical Constriction in C. elegans by Linking Developmental Patterning to Force Generation.

Authors:  Daniel J Marston; Christopher D Higgins; Kimberly A Peters; Timothy D Cupp; Daniel J Dickinson; Ariel M Pani; Regan P Moore; Amanda H Cox; Daniel P Kiehart; Bob Goldstein
Journal:  Curr Biol       Date:  2016-07-21       Impact factor: 10.834

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