Literature DB >> 20697954

Dyslexia-associated kiaa0319-like protein interacts with axon guidance receptor nogo receptor 1.

Ming-Wai Poon1, Wan-Hong Tsang, Sun-On Chan, Hiu-Ming Li, Ho-Keung Ng, Mary Miu-Yee Waye.   

Abstract

To identify the putative interacting partners for Kiaa0319-like protein. KIAA0319-like, located near the dyslexia susceptibility locus, DYX8 in chromosome 1p34.3, has been suggested as a positional candidate for developmental dyslexia due to its homology with another gene, KIAA0319 which has been strongly established as a candidate gene for developmental dyslexia. Previous research has shown that a single marker, rs7523017 (P = 0.042) has been associated with developmental dyslexia by a Canadian group. There is little functional information about this gene and protein. In this article, we put forward further evidence that support Kiaa0319-like is a candidate for this disorder. A yeast-2-hybrid screen and co-immunopreciptiation assays were performed to find protein interacting partners of KIAA0319L. A human cortex immunohistochemistry assay was performed to show the colocalization of Kiaa0319-like and its specific interacting partner in cells. Nogo Receptor 1 (NgR1), an axon guidance receptor, was identified to have physical interactions with Kiaa0319-like protein. These two proteins interact predominantly in the cytoplasmic granules of cortical neurons in the human brain cortex. Based on this data, it can be concluded that Kiaa0319-like protein interacts with Nogo Receptor 1, supporting the idea that Kiaa0319-like protein participates in axon guidance.

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Year:  2010        PMID: 20697954     DOI: 10.1007/s10571-010-9549-1

Source DB:  PubMed          Journal:  Cell Mol Neurobiol        ISSN: 0272-4340            Impact factor:   5.046


  44 in total

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Authors:  Sha Mi; Xinhua Lee; Zhaohui Shao; Greg Thill; Benxiu Ji; Jane Relton; Melissa Levesque; Norm Allaire; Steve Perrin; Bryan Sands; Thomas Crowell; Richard L Cate; John M McCoy; R Blake Pepinsky
Journal:  Nat Neurosci       Date:  2004-02-15       Impact factor: 24.884

Review 2.  Neuronal growth-promoting and inhibitory cues in neuroprotection and neuroregeneration.

Authors:  Stephen D Skaper
Journal:  Ann N Y Acad Sci       Date:  2005-08       Impact factor: 5.691

3.  DYX1C1 functions in neuronal migration in developing neocortex.

Authors:  Y Wang; M Paramasivam; A Thomas; J Bai; N Kaminen-Ahola; J Kere; J Voskuil; G D Rosen; A M Galaburda; J J Loturco
Journal:  Neuroscience       Date:  2006-09-20       Impact factor: 3.590

4.  Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

Authors:  Natalie Cope; Denise Harold; Gary Hill; Valentina Moskvina; Jim Stevenson; Peter Holmans; Michael J Owen; Michael C O'Donovan; Julie Williams
Journal:  Am J Hum Genet       Date:  2005-02-16       Impact factor: 11.025

5.  Chemorepulsion of axons in the developing mammalian central nervous system.

Authors:  A Pini
Journal:  Science       Date:  1993-07-02       Impact factor: 47.728

6.  Structure of the Nogo receptor ectodomain: a recognition module implicated in myelin inhibition.

Authors:  Xiaolin L He; J Fernando Bazan; Gerry McDermott; Jong Bae Park; Kevin Wang; Marc Tessier-Lavigne; Zhigang He; K Christopher Garcia
Journal:  Neuron       Date:  2003-04-24       Impact factor: 17.173

7.  The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities.

Authors:  Jillian M Couto; Lissette Gomez; Karen Wigg; Tasha Cate-Carter; Jennifer Archibald; Barbara Anderson; Rosemary Tannock; Elizabeth N Kerr; Maureen W Lovett; Tom Humphries; Cathy L Barr
Journal:  J Neurogenet       Date:  2008       Impact factor: 1.250

8.  Nogo receptor 1 regulates formation of lasting memories.

Authors:  Alexandra Karlén; Tobias E Karlsson; Anna Mattsson; Karin Lundströmer; Simone Codeluppi; Therese M Pham; Cristina M Bäckman; Sven Ove Ogren; Elin Aberg; Alexander F Hoffman; Michael A Sherling; Carl R Lupica; Barry J Hoffer; Christian Spenger; Anna Josephson; Stefan Brené; Lars Olson
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-13       Impact factor: 11.205

9.  Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

Authors:  Silvia Paracchini; Colin D Steer; Lyn-Louise Buckingham; Andrew P Morris; Susan Ring; Thomas Scerri; John Stein; Marcus E Pembrey; Jiannis Ragoussis; Jean Golding; Anthony P Monaco
Journal:  Am J Psychiatry       Date:  2008-10-01       Impact factor: 18.112

10.  The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.

Authors:  Silvia Paracchini; Ankur Thomas; Sandra Castro; Cecilia Lai; Murugan Paramasivam; Yu Wang; Brendan J Keating; Jennifer M Taylor; Douglas F Hacking; Thomas Scerri; Clyde Francks; Alex J Richardson; Richard Wade-Martins; John F Stein; Julian C Knight; Andrew J Copp; Joseph Loturco; Anthony P Monaco
Journal:  Hum Mol Genet       Date:  2006-04-06       Impact factor: 6.150

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  16 in total

1.  The Roles of Genes in the Neuronal Migration and Neurite Outgrowth Network in Developmental Dyslexia: Single- and Multiple-Risk Genetic Variants.

Authors:  Shanshan Shao; Rui Kong; Li Zou; Rong Zhong; Jiao Lou; Jie Zhou; Shengnan Guo; Jia Wang; Xiaohui Zhang; Jiajia Zhang; Ranran Song
Journal:  Mol Neurobiol       Date:  2015-07-17       Impact factor: 5.590

2.  KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.

Authors:  Sara Mascheretti; Valentina Riva; Roberto Giorda; Silvana Beri; Lara Francesca Emilia Lanzoni; Maria Rosaria Cellino; Cecilia Marino
Journal:  J Hum Genet       Date:  2014-01-16       Impact factor: 3.172

3.  AAVR: A Multi-Serotype Receptor for AAV.

Authors:  Candace Summerford; Jarrod S Johnson; R Jude Samulski
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4.  Neuroimaging genetics studies of specific reading disability and developmental language disorder: A review.

Authors:  Nicole Landi; Meaghan Perdue
Journal:  Lang Linguist Compass       Date:  2019-09-05

5.  Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders.

Authors:  M P Platt; W T Adler; A J Mehlhorn; G C Johnson; K A Wright; R T Choi; W H Tsang; M W Poon; S Y Yeung; M M Y Waye; A M Galaburda; G D Rosen
Journal:  Neuroscience       Date:  2013-07-03       Impact factor: 3.590

Review 6.  Cryo-electron Microscopy of Adeno-associated Virus.

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7.  An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.

Authors:  S Mascheretti; A Bureau; V Trezzi; R Giorda; C Marino
Journal:  Hum Genet       Date:  2015-04-28       Impact factor: 4.132

8.  Knockdown of the dyslexia-associated gene Kiaa0319 impairs temporal responses to speech stimuli in rat primary auditory cortex.

Authors:  T M Centanni; A B Booker; A M Sloan; F Chen; B J Maher; R S Carraway; N Khodaparast; R Rennaker; J J LoTurco; M P Kilgard
Journal:  Cereb Cortex       Date:  2013-02-08       Impact factor: 5.357

9.  The genetics of reading disabilities: from phenotypes to candidate genes.

Authors:  Wendy H Raskind; Beate Peter; Todd Richards; Mark M Eckert; Virginia W Berninger
Journal:  Front Psychol       Date:  2013-01-07

10.  Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

Authors:  Elizabeth A Worthey; Gordana Raca; Jennifer J Laffin; Brandon M Wilk; Jeremy M Harris; Kathy J Jakielski; David P Dimmock; Edythe A Strand; Lawrence D Shriberg
Journal:  J Neurodev Disord       Date:  2013-10-02       Impact factor: 4.025

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