Literature DB >> 15105459

Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis.

Joanna C Jen1, Wai-Man Chan, Thomas M Bosley, Jijun Wan, Janai R Carr, Udo Rüb, David Shattuck, Georges Salamon, Lili C Kudo, Jing Ou, Doris D M Lin, Mustafa A M Salih, Tülay Kansu, Hesham Al Dhalaan, Zayed Al Zayed, David B MacDonald, Bent Stigsby, Andreas Plaitakis, Emmanuel K Dretakis, Irene Gottlob, Christina Pieh, Elias I Traboulsi, Qing Wang, Lejin Wang, Caroline Andrews, Koki Yamada, Joseph L Demer, Shaheen Karim, Jeffry R Alger, Daniel H Geschwind, Thomas Deller, Nancy L Sicotte, Stanley F Nelson, Robert W Baloh, Elizabeth C Engle.   

Abstract

The mechanisms controlling axon guidance are of fundamental importance in understanding brain development. Growing corticospinal and somatosensory axons cross the midline in the medulla to reach their targets and thus form the basis of contralateral motor control and sensory input. The motor and sensory projections appeared uncrossed in patients with horizontal gaze palsy with progressive scoliosis (HGPPS). In patients affected with HGPPS, we identified mutations in the ROBO3 gene, which shares homology with roundabout genes important in axon guidance in developing Drosophila, zebrafish, and mouse. Like its murine homolog Rig1/Robo3, but unlike other Robo proteins, ROBO3 is required for hindbrain axon midline crossing.

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Year:  2004        PMID: 15105459      PMCID: PMC1618874          DOI: 10.1126/science.1096437

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  24 in total

Review 1.  Axon guidance: the cytoplasmic tail.

Authors:  Bharatkumar N Patel; David L Van Vactor
Journal:  Curr Opin Cell Biol       Date:  2002-04       Impact factor: 8.382

2.  Rig-1 a new member of Robo family genes exhibits distinct pattern of expression during mouse development.

Authors:  Laura Camurri; Elvira Mambetisaeva; Vasi Sundaresan
Journal:  Gene Expr Patterns       Date:  2004-01       Impact factor: 1.224

3.  Brainstem hypoplasia in familial horizontal gaze palsy and scoliosis.

Authors:  C Pieh; D Lengyel; A Neff; C Fretz; I Gottlob
Journal:  Neurology       Date:  2002-08-13       Impact factor: 9.910

4.  Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).

Authors:  Koki Yamada; Caroline Andrews; Wai-Man Chan; Craig A McKeown; Adriano Magli; Teresa de Berardinis; Anat Loewenstein; Moshe Lazar; Michael O'Keefe; Robert Letson; Arnold London; Mark Ruttum; Naomichi Matsumoto; Nakamichi Saito; Lisa Morris; Monte Del Monte; Roger H Johnson; Eiichiro Uyama; Willem A Houtman; Berendina de Vries; Thomas J Carlow; Blaine L Hart; Nicolas Krawiecki; John Shoffner; Marlene C Vogel; James Katowitz; Scott M Goldstein; Alex V Levin; Emin C Sener; Banu T Ozturk; A Nurten Akarsu; Michael C Brodsky; Frank Hanisch; Robert P Cruse; Alina A Zubcov; Richard M Robb; Peter Roggenkäemper; Irene Gottlob; Lionel Kowal; Ravi Battu; Elias I Traboulsi; Piergiorgio Franceschini; Anna Newlin; Joseph L Demer; Elizabeth C Engle
Journal:  Nat Genet       Date:  2003-11-02       Impact factor: 38.330

5.  Congenital scoliosis associated with encephalopathy in five children of two families.

Authors:  E K Dretakis; P N Kondoyannis
Journal:  J Bone Joint Surg Am       Date:  1974-12       Impact factor: 5.284

6.  Familial paralysis of horizontal gaze. Associated with pendular nystagmus, progressive scoliosis, and facial contraction with myokymia.

Authors:  J A Sharpe; J L Silversides; R D Blair
Journal:  Neurology       Date:  1975-11       Impact factor: 9.910

7.  The divergent Robo family protein rig-1/Robo3 is a negative regulator of slit responsiveness required for midline crossing by commissural axons.

Authors:  Christelle Sabatier; Andrew S Plump; Katja Brose; Atsushi Tamada; Fujio Murakami; Eva Y-H P Lee; Marc Tessier-Lavigne
Journal:  Cell       Date:  2004-04-16       Impact factor: 41.582

8.  Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25.

Authors:  Joanna Jen; C J Coulin; T M Bosley; M A M Salih; C Sabatti; S F Nelson; R W Baloh
Journal:  Neurology       Date:  2002-08-13       Impact factor: 9.910

9.  A Leu7Pro mutation in the signal peptide of platelet glycoprotein (GP)IX in a case of Bernard-Soulier syndrome abolishes surface expression of the GPIb-V-IX complex.

Authors:  François Lanza; Corinne De La Salle; Marie-Jeanne Baas; Agnès Schwartz; Bernadette Boval; Jean-Pierre Cazenave; Jacques P Caen
Journal:  Br J Haematol       Date:  2002-07       Impact factor: 6.998

10.  Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family.

Authors:  Raidah Al-Baradie; Koki Yamada; Cynthia St Hilaire; Wai-Man Chan; Caroline Andrews; Nathalie McIntosh; Motoi Nakano; E Jean Martonyi; William R Raymond; Sada Okumura; Michael M Okihiro; Elizabeth C Engle
Journal:  Am J Hum Genet       Date:  2002-10-22       Impact factor: 11.025

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  115 in total

Review 1.  Wiring the Human Brain: A User's Handbook.

Authors:  Raphael M Bendriem; M Elizabeth Ross
Journal:  Neuron       Date:  2017-08-02       Impact factor: 17.173

2.  Analysis of the CHN1 gene in patients with various types of congenital ocular motility disorders.

Authors:  Alexander E Volk; Julia Fricke; Judith Strobl; Gerold Kolling; Christian Kubisch; Antje Neugebauer
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2010-06-10       Impact factor: 3.117

3.  Inhibition of medulloblastoma cell invasion by Slit.

Authors:  T E Werbowetski-Ogilvie; M Seyed Sadr; N Jabado; A Angers-Loustau; N Y R Agar; J Wu; R Bjerkvig; J P Antel; D Faury; Y Rao; R F Del Maestro
Journal:  Oncogene       Date:  2006-04-24       Impact factor: 9.867

4.  Wildervanck's syndrome and mirror movements: a congenital disorder of axon migration?

Authors:  Tobias Högen; Wai-Man Chan; Eva Riedel; Roland Brüning; Hannah H Chang; Elizabeth C Engle; Adrian Danek
Journal:  J Neurol       Date:  2011-09-23       Impact factor: 4.849

5.  Binding site for Robo receptors revealed by dissection of the leucine-rich repeat region of Slit.

Authors:  Jason A Howitt; Naomi J Clout; Erhard Hohenester
Journal:  EMBO J       Date:  2004-10-21       Impact factor: 11.598

6.  Analysis of the brain-stem white-matter tracts with diffusion tensor imaging.

Authors:  N Salamon; N Sicotte; J Alger; D Shattuck; S Perlman; U Sinha; H Schultze-Haakh; G Salamon
Journal:  Neuroradiology       Date:  2005-09-13       Impact factor: 2.804

Review 7.  Can regenerating axons recapitulate developmental guidance during recovery from spinal cord injury?

Authors:  Noam Y Harel; Stephen M Strittmatter
Journal:  Nat Rev Neurosci       Date:  2006-08       Impact factor: 34.870

8.  Two pedigrees segregating Duane's retraction syndrome as a dominant trait map to the DURS2 genetic locus.

Authors:  Elizabeth C Engle; Caroline Andrews; Krystal Law; Joseph L Demer
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-01       Impact factor: 4.799

9.  Clinical characterization of the HOXA1 syndrome BSAS variant.

Authors:  T M Bosley; M A Salih; I A Alorainy; D T Oystreck; M Nester; K K Abu-Amero; M A Tischfield; E C Engle
Journal:  Neurology       Date:  2007-09-18       Impact factor: 9.910

10.  Mirror movement-like defects in startle behavior of zebrafish dcc mutants are caused by aberrant midline guidance of identified descending hindbrain neurons.

Authors:  Roshan A Jain; Hannah Bell; Amy Lim; Chi-Bin Chien; Michael Granato
Journal:  J Neurosci       Date:  2014-02-19       Impact factor: 6.167

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