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

Am J Hum Genet
Authors
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.

Year of Publication
2016
Journal
Am J Hum Genet
Volume
98
Issue
6
Pages
1220-7
Date Published
2016 Jun 02
ISSN
1537-6605
URL
DOI
10.1016/j.ajhg.2016.03.023
PubMed ID
27181683
PubMed Central ID
PMC4908193
Links
Grant list
P30 HD018655 / HD / NICHD NIH HHS / United States
R01 EY012498 / EY / NEI NIH HHS / United States
U54 HD090255 / HD / NICHD NIH HHS / United States