Literature DB >> 27181683

Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects.

Jong G Park1, Max A Tischfield2, Alicia A Nugent3, Long Cheng4, Silvio Alessandro Di Gioia2, Wai-Man Chan5, Gail Maconachie6, Thomas M Bosley7, C Gail Summers8, David G Hunter9, Caroline D Robson10, Irene Gottlob6, Elizabeth C Engle11.   

Abstract

Duane retraction syndrome (DRS) is a congenital eye-movement disorder defined by limited outward gaze and retraction of the eye on attempted inward gaze. Here, we report on three heterozygous loss-of-function MAFB mutations causing DRS and a dominant-negative MAFB mutation causing DRS and deafness. Using genotype-phenotype correlations in humans and Mafb-knockout mice, we propose a threshold model for variable loss of MAFB function. Postmortem studies of DRS have reported abducens nerve hypoplasia and aberrant innervation of the lateral rectus muscle by the oculomotor nerve. Our studies in mice now confirm this human DRS pathology. Moreover, we demonstrate that selectively disrupting abducens nerve development is sufficient to cause secondary innervation of the lateral rectus muscle by aberrant oculomotor nerve branches, which form at developmental decision regions close to target extraocular muscles. Thus, we present evidence that the primary cause of DRS is failure of the abducens nerve to fully innervate the lateral rectus muscle in early development.
Copyright © 2016 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27181683      PMCID: PMC4908193          DOI: 10.1016/j.ajhg.2016.03.023

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  33 in total

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Journal:  Nature       Date:  1997-05-08       Impact factor: 49.962

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Journal:  Mol Cell Biol       Date:  1994-01       Impact factor: 4.272

8.  Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome.

Authors:  Noriko Miyake; John Chilton; Maria Psatha; Long Cheng; Caroline Andrews; Wai-Man Chan; Krystal Law; Moira Crosier; Susan Lindsay; Michelle Cheung; James Allen; Nick J Gutowski; Sian Ellard; Elizabeth Young; Alessandro Iannaccone; Binoy Appukuttan; J Timothy Stout; Stephen Christiansen; Maria Laura Ciccarelli; Alfonso Baldi; Mara Campioni; Juan C Zenteno; Dominic Davenport; Laura E Mariani; Mustafa Sahin; Sarah Guthrie; Elizabeth C Engle
Journal:  Science       Date:  2008-07-24       Impact factor: 47.728

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

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Journal:  Am J Hum Genet       Date:  2002-10-22       Impact factor: 11.025

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Authors:  I J McKay; I Muchamore; R Krumlauf; M Maden; A Lumsden; J Lewis
Journal:  Development       Date:  1994-08       Impact factor: 6.868

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  19 in total

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Authors:  Alicia A Nugent; Jong G Park; Yan Wei; Alan P Tenney; Nicole M Gilette; Michelle M DeLisle; Wai-Man Chan; Long Cheng; Elizabeth C Engle
Journal:  J Clin Invest       Date:  2017-03-27       Impact factor: 14.808

2.  Decreased ACKR3 (CXCR7) function causes oculomotor synkinesis in mice and humans.

Authors:  Mary C Whitman; Noriko Miyake; Elaine H Nguyen; Jessica L Bell; Paola M Matos Ruiz; Wai-Man Chan; Silvio Alessandro Di Gioia; Nisha Mukherjee; Brenda J Barry; T M Bosley; Arif O Khan; Elizabeth C Engle
Journal:  Hum Mol Genet       Date:  2019-09-15       Impact factor: 6.150

Review 3.  Ocular congenital cranial dysinnervation disorders (CCDDs): insights into axon growth and guidance.

Authors:  Mary C Whitman; Elizabeth C Engle
Journal:  Hum Mol Genet       Date:  2017-08-01       Impact factor: 6.150

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Authors:  Suohui Sun; Hui Guo; Nan Liang; Tao Wu; Chunpu Zhang; Huaqing Li
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5.  Multicentric Carpotarsal Osteolysis Syndrome in a Mother and Daughter with a MAFB Missense Variant and Natural History of the Disease.

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Journal:  Mol Syndromol       Date:  2021-08-27

6.  MafB Is Critical for Glucagon Production and Secretion in Mouse Pancreatic α Cells In Vivo.

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Journal:  Mol Cell Biol       Date:  2018-03-29       Impact factor: 4.272

7.  Identification of a novel CHN1 p.(Phe213Val) variant in a large Han Chinese family with congenital Duane retraction syndrome.

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Review 8.  Axonal Growth Abnormalities Underlying Ocular Cranial Nerve Disorders.

Authors:  Mary C Whitman
Journal:  Annu Rev Vis Sci       Date:  2021-06-03       Impact factor: 7.745

Review 9.  The emerging role of cranial nerves in shaping craniofacial development.

Authors:  Sonia Sudiwala; Sarah M Knox
Journal:  Genesis       Date:  2019-01       Impact factor: 2.389

10.  The Mafb cleft-associated variant H131Q is not required for palatogenesis in the mouse.

Authors:  Brian J Paul; Kristina J Palmer; Lindsey Rhea; Melissa Carlson; Jocelyn C Sharp; C Herbert Pratt; Stephen A Murray; Martine Dunnwald
Journal:  Dev Dyn       Date:  2021-03-27       Impact factor: 2.842

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