Literature DB >> 12949137

Identification of Nogo-66 receptor (NgR) and homologous genes in fish.

Michael Klinger1, John S Taylor, Thomas Oertle, Martin E Schwab, Claudia A O Stuermer, Heike Diekmann.   

Abstract

The Nogo-66 receptor NgR has been implicated in the mediation of inhibitory effects of central nervous system (CNS) myelin on axon growth in the adult mammalian CNS. NgR binds to several myelin-associated ligands (Nogo-66, myelin associated glycoprotein, and oligodendrocyte-myelin glycoprotein), which, among other inhibitory proteins, impair axonal regeneration in the CNS of adult mammals. In contrast to mammals, severed axons readily regenerate in the fish CNS. Nevertheless, fish axons are repelled by mammalian oligodendrocytes in vitro. Therefore, the identification of fish NgR homologs is a crucial step towards understanding NgR functions in vertebrate systems competent of CNS regeneration. Here, we report the discovery of four zebrafish (Danio rerio) and five fugu (Takifugu rubripes) NgR homologs. Synteny between fish and human, comparable intron-exon structures, and phylogenetic analyses provide convincing evidence that the true fish orthologs were identified. The topology of the phylogenetic trees shows that the extra fish genes were produced by duplication events that occurred in ray-finned fishes before the divergence of the zebrafish and pufferfish lineages. Expression of zebrafish NgR homologs was detected relatively early in development and prominently in the adult brain, suggesting functions in axon growth, guidance, or plasticity.

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Year:  2003        PMID: 12949137     DOI: 10.1093/molbev/msg241

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  8 in total

1.  The Nogo-66 receptor homolog NgR2 is a sialic acid-dependent receptor selective for myelin-associated glycoprotein.

Authors:  Karthik Venkatesh; Onanong Chivatakarn; Hakjoo Lee; Pushkar S Joshi; David B Kantor; Barbara A Newman; Rose Mage; Christoph Rader; Roman J Giger
Journal:  J Neurosci       Date:  2005-01-26       Impact factor: 6.167

2.  Crystal structure of the Nogo-receptor-2.

Authors:  Mariya Semavina; Nayanendu Saha; Momchil V Kolev; Yehuda Goldgur; Roman J Giger; Juha P Himanen; Dimitar B Nikolov
Journal:  Protein Sci       Date:  2011-04       Impact factor: 6.725

3.  Identification and characterization of alternative promoters of zebrafish Rtn-4/Nogo genes in cultured cells and zebrafish embryos.

Authors:  Yi-Chung Chen; Bo-Kai Wu; Cheng-Ying Chu; Chia-Hsiung Cheng; Hau-Wei Han; Gen-Der Chen; Ming-Ting Lee; Pung-Pung Hwang; Koichi Kawakami; Chun-Che Chang; Chang-Jen Huang
Journal:  Nucleic Acids Res       Date:  2010-04-08       Impact factor: 16.971

4.  Inhibition of retinal ganglion cell axonal outgrowth through the Amino-Nogo-A signaling pathway.

Authors:  Yan Huo; Xiao-Lei Yin; Shu-Xing Ji; Huan Zou; Min Lang; Zheng Zheng; Xiao-Feng Cai; Wei Liu; Chun-Lin Chen; Yuan-Guo Zhou; Rong-Di Yuan; Jian Ye
Journal:  Neurochem Res       Date:  2013-04-12       Impact factor: 3.996

5.  NOGO-A induction and localization during chick brain development indicate a role disparate from neurite outgrowth inhibition.

Authors:  Shelley A Caltharp; Charmaine U Pira; Noboru Mishima; Erik N Youngdale; David S McNeill; Boleslaw H Liwnicz; Kerby C Oberg
Journal:  BMC Dev Biol       Date:  2007-04-14       Impact factor: 1.978

6.  Essential roles of zebrafish rtn4/Nogo paralogues in embryonic development.

Authors:  Alejandro Pinzón-Olejua; Cornelia Welte; Houari Abdesselem; Edward Málaga-Trillo; Claudia Ao Stuermer
Journal:  Neural Dev       Date:  2014-04-23       Impact factor: 3.842

7.  Developmentally regulated impediments to skin reinnervation by injured peripheral sensory axon terminals.

Authors:  Georgeann S O'Brien; Seanna M Martin; Christian Söllner; Gavin J Wright; Catherina G Becker; Carlos Portera-Cailliau; Alvaro Sagasti
Journal:  Curr Biol       Date:  2009-12-03       Impact factor: 10.834

8.  The Nogo-C2/Nogo receptor complex regulates the morphogenesis of zebrafish lateral line primordium through modulating the expression of dkk1b, a Wnt signal inhibitor.

Authors:  Hao-Wei Han; Chih-Ming Chou; Cheng-Ying Chu; Chia-Hsiung Cheng; Chung-Hsiang Yang; Chin-Chun Hung; Pung-Pung Hwang; Shyh-Jye Lee; Yung-Feng Liao; Chang-Jen Huang
Journal:  PLoS One       Date:  2014-01-21       Impact factor: 3.240

  8 in total

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