Literature DB >> 26735242

Structure of developmental gene regulatory networks from the perspective of cell fate-determining genes.

Mercedes Martín1, María F Organista1, Jose F de Celis1.   

Abstract

The core of gene regulatory networks (GRNs) is formed by transcription factors (TF) and cis-regulatory modules (CRMs) present in their downstream genes. GRNs have a modular structure in which complex circuitries link TFs to CRMs to generate specific transcriptional outputs. (1) Of particular interest are those GRNs including cell fate-determining genes, as they constitute developmental switches which activity is necessary and sufficient to promote particular cellular fates. Most of the genetic analysis of developmental processes deals with the composition and structure of GRNs acting upstream of cell fate-determining genes, as they are best suited for genetic analysis and molecular deconstruction. More recently, the application of a variety of in vivo, computational and genome-wide approaches is allowing the identification and functional analysis of GRNs acting downstream of cell fate-determining genes. In this review we discuss several examples of GRNs acting upstream and downstream of cell fate-determining genes, including other TFs which activity pervade across both regulatory networks.

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Year:  2016        PMID: 26735242      PMCID: PMC4802764          DOI: 10.1080/21541264.2015.1130118

Source DB:  PubMed          Journal:  Transcription        ISSN: 2154-1272


  27 in total

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Authors:  B Sanson
Journal:  EMBO Rep       Date:  2001-12       Impact factor: 8.807

2.  Genetic control of wing disc development in Drosophila.

Authors:  A García-Bellido
Journal:  Ciba Found Symp       Date:  1975

Review 3.  Half a century of neural prepatterning: the story of a few bristles and many genes.

Authors:  José Luis Gómez-Skarmeta; Sonsoles Campuzano; Juan Modolell
Journal:  Nat Rev Neurosci       Date:  2003-07       Impact factor: 34.870

4.  Knockdown of spalt function by RNAi causes de-repression of Hox genes and homeotic transformations in the crustacean Artemia franciscana.

Authors:  Tijana Copf; Nicolas Rabet; Michalis Averof
Journal:  Dev Biol       Date:  2006-07-28       Impact factor: 3.582

Review 5.  Genomic evolution of Hox gene clusters.

Authors:  Derek Lemons; William McGinnis
Journal:  Science       Date:  2006-09-29       Impact factor: 47.728

6.  ovo/svb integrates Wingless and DER pathways to control epidermis differentiation.

Authors:  F Payre; A Vincent; S Carreno
Journal:  Nature       Date:  1999-07-15       Impact factor: 49.962

7.  sem-4 promotes vulval cell-fate determination in Caenorhabditis elegans through regulation of lin-39 Hox.

Authors:  K Grant; W Hanna-Rose; M Han
Journal:  Dev Biol       Date:  2000-08-15       Impact factor: 3.582

8.  The Caenorhabditis elegans spalt-like gene sem-4 restricts touch cell fate by repressing the selector Hox gene egl-5 and the effector gene mec-3.

Authors:  Anne S Toker; Yingqi Teng; Henrique B Ferreira; Scott W Emmons; Martin Chalfie
Journal:  Development       Date:  2003-08       Impact factor: 6.868

9.  Shavenbaby couples patterning to epidermal cell shape control.

Authors:  Hélène Chanut-Delalande; Isabelle Fernandes; Fernando Roch; François Payre; Serge Plaza
Journal:  PLoS Biol       Date:  2006-09       Impact factor: 8.029

10.  Hox repression of a target gene: extradenticle-independent, additive action through multiple monomer binding sites.

Authors:  Ron Galant; Christopher M Walsh; Sean B Carroll
Journal:  Development       Date:  2002-07       Impact factor: 6.868

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  1 in total

1.  Single-cell transcriptomic signatures and gene regulatory networks modulated by Wls in mammalian midline facial formation and clefts.

Authors:  Ran Gu; Shuwen Zhang; Subbroto Kumar Saha; Yu Ji; Kurt Reynolds; Moira McMahon; Bo Sun; Mohammad Islam; Paul A Trainor; YiPing Chen; Ying Xu; Yang Chai; Diana Burkart-Waco; Chengji J Zhou
Journal:  Development       Date:  2022-07-22       Impact factor: 6.862

  1 in total

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