Literature DB >> 18606137

Signal-induced repression: the exception or the rule in developmental signaling?

Markus Affolter1, George Pyrowolakis, Alexander Weiss, Konrad Basler.   

Abstract

Cell-cell communication plays a key role in organ formation and patterning in multicellular animals and is carried out by a few evolutionarily conserved signaling pathways. The modes of action of these pathways share a number of general properties, or habits, that allow them to strongly activate target genes in a ligand-dependent manner in the proper cellular contexts. Recent studies have revealed that some developmental signaling pathways can also strongly repress genes in a ligand-dependent manner. These new findings raise the interesting possibility that this repressive mode of action is shared by many or most developmental signaling pathways.

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Year:  2008        PMID: 18606137     DOI: 10.1016/j.devcel.2008.06.006

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  18 in total

Review 1.  Wnt/Wingless signaling in Drosophila.

Authors:  Sharan Swarup; Esther M Verheyen
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-06-01       Impact factor: 10.005

2.  T(H)2 bias: Mina tips the balance.

Authors:  Saskia Hemmers; Kerri A Mowen
Journal:  Nat Immunol       Date:  2009-08       Impact factor: 25.606

3.  Hyphal chain formation in Candida albicans: Cdc28-Hgc1 phosphorylation of Efg1 represses cell separation genes.

Authors:  Allen Wang; Prashna Pala Raniga; Shelley Lane; Yang Lu; Haoping Liu
Journal:  Mol Cell Biol       Date:  2009-06-15       Impact factor: 4.272

Review 4.  Transcriptional Control by the SMADs.

Authors:  Caroline S Hill
Journal:  Cold Spring Harb Perspect Biol       Date:  2016-10-03       Impact factor: 10.005

Review 5.  The Capicua repressor--a general sensor of RTK signaling in development and disease.

Authors:  Gerardo Jiménez; Stanislav Y Shvartsman; Ze'ev Paroush
Journal:  J Cell Sci       Date:  2012-03-15       Impact factor: 5.285

6.  Nuclear receptor corepressors Ncor1 and Ncor2 (Smrt) are required for retinoic acid-dependent repression of Fgf8 during somitogenesis.

Authors:  Sandeep Kumar; Thomas J Cunningham; Gregg Duester
Journal:  Dev Biol       Date:  2016-08-06       Impact factor: 3.582

7.  Retinoic acid controls body axis extension by directly repressing Fgf8 transcription.

Authors:  Sandeep Kumar; Gregg Duester
Journal:  Development       Date:  2014-08       Impact factor: 6.868

8.  The TEA domain family transcription factor TEAD4 represses murine adipogenesis by recruiting the cofactors VGLL4 and CtBP2 into a transcriptional complex.

Authors:  Wenxiang Zhang; Jinjin Xu; Jinhui Li; Tong Guo; Dan Jiang; Xue Feng; Xueyan Ma; Lingli He; Wenqing Wu; Mengxin Yin; Ling Ge; Zuoyun Wang; Margaret S Ho; Yun Zhao; Zhaoliang Fei; Lei Zhang
Journal:  J Biol Chem       Date:  2018-09-12       Impact factor: 5.157

9.  The Hippo effector Yorkie controls normal tissue growth by antagonizing scalloped-mediated default repression.

Authors:  Laura M Koontz; Yi Liu-Chittenden; Feng Yin; Yonggang Zheng; Jianzhong Yu; Bo Huang; Qian Chen; Shian Wu; Duojia Pan
Journal:  Dev Cell       Date:  2013-05-28       Impact factor: 12.270

10.  Global analysis of alternative splicing regulation by insulin and wingless signaling in Drosophila cells.

Authors:  Britta Hartmann; Robert Castelo; Marco Blanchette; Stephanie Boue; Donald C Rio; Juan Valcárcel
Journal:  Genome Biol       Date:  2009-01-29       Impact factor: 13.583

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