Literature DB >> 17374844

Single mage gene in the chicken genome encodes CMage, a protein with functional similarities to mammalian type II Mage proteins.

Noelia López-Sánchez1, Zaira González-Fernández, Michio Niinobe, Kazuaki Yoshikawa, José María Frade.   

Abstract

In mammals, the type II melanoma antigen (Mage) protein family is constituted by at least 10 closely related members that are expressed in different tissues, including the nervous system. These proteins are believed to regulate cell cycle withdrawal, neuronal differentiation, and apoptosis. However, the analysis of their specific function has been complicated by functional redundancy. In accordance with previous studies in teleosts and Drosophila, we present evidence that only one mage gene exists in genomes from protists, fungi, plants, nematodes, insects, and nonmammalian vertebrates. We have identified the chicken mage gene and cloned the cDNA encoding the chick Mage protein (CMage). CMage shares close homology with the type II Mage protein family, and, as previously shown for the type II Mage proteins Necdin and Mage-G1, it can interact with the transcription factor E2F-1. CMage is expressed in specific regions of the developing nervous system including the retinal ganglion cell layer, the ventral horn of the spinal cord, and the dorsal root ganglia, coinciding with the expression of the neurotrophin receptor p75 (p75(NTR)) in these regions. We show that the intracellular domain of p75(NTR) can interact with both CMage and Necdin, thus preventing the binding of the latter proteins to the transcription factor E2F-1, and facilitating the proapoptotic activity of E2F-1 in N1E-115 differentiating neurons. The presence of a single mage gene in the chicken genome, together with the close functional resemblance between CMage and Necdin, makes this species ideal to further analyze signal transduction through type II Mage proteins.

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Year:  2007        PMID: 17374844     DOI: 10.1152/physiolgenomics.00249.2006

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  22 in total

1.  Nerve growth factor-induced cell cycle reentry in newborn neurons is triggered by p38MAPK-dependent E2F4 phosphorylation.

Authors:  Sandra M Morillo; Erika P Abanto; María J Román; José M Frade
Journal:  Mol Cell Biol       Date:  2012-05-14       Impact factor: 4.272

2.  Somatic tetraploidy in specific chick retinal ganglion cells induced by nerve growth factor.

Authors:  Sandra M Morillo; Pedro Escoll; Antonio de la Hera; José M Frade
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-14       Impact factor: 11.205

3.  Molecular evolution of type II MAGE genes from ancestral MAGED2 gene and their phylogenetic resolution of basal mammalian clades.

Authors:  Marcos De Donato; Sunday O Peters; Tanveer Hussain; Hectorina Rodulfo; Bolaji N Thomas; Masroor E Babar; Ikhide G Imumorin
Journal:  Mamm Genome       Date:  2017-05-17       Impact factor: 2.957

Review 4.  Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.

Authors:  Klementina Fon Tacer; Patrick Ryan Potts
Journal:  Biochem J       Date:  2017-06-16       Impact factor: 3.857

5.  MAGE-RING protein complexes comprise a family of E3 ubiquitin ligases.

Authors:  Jennifer M Doyle; Jinlan Gao; Jiawei Wang; Maojun Yang; Patrick Ryan Potts
Journal:  Mol Cell       Date:  2010-09-24       Impact factor: 17.970

6.  Somatic tetraploidy in vertebrate neurons: Implications in physiology and pathology.

Authors:  José María Frade
Journal:  Commun Integr Biol       Date:  2010-03

Review 7.  When MAGE meets RING: insights into biological functions of MAGE proteins.

Authors:  Yue Feng; Jinlan Gao; Maojun Yang
Journal:  Protein Cell       Date:  2011-02-20       Impact factor: 14.870

8.  A direct comparison of strategies for combinatorial RNA interference.

Authors:  Luke S Lambeth; Nick J Van Hateren; Stuart A Wilson; Venugopal Nair
Journal:  BMC Mol Biol       Date:  2010-10-11       Impact factor: 2.946

Review 9.  Emerging roles of the MAGE protein family in stress response pathways.

Authors:  Rebecca R Florke Gee; Helen Chen; Anna K Lee; Christina A Daly; Benjamin A Wilander; Klementina Fon Tacer; Patrick Ryan Potts
Journal:  J Biol Chem       Date:  2020-09-13       Impact factor: 5.157

10.  NRAGE, a p75NTR adaptor protein, is required for developmental apoptosis in vivo.

Authors:  M J M Bertrand; R S Kenchappa; D Andrieu; M Leclercq-Smekens; H N T Nguyen; B D Carter; F Muscatelli; P A Barker; O De Backer
Journal:  Cell Death Differ       Date:  2008-09-05       Impact factor: 15.828

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