Literature DB >> 19892780

The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development.

Joanne Betts-Henderson1, Stefano Bartesaghi, Moira Crosier, Susan Lindsay, Hai-Lan Chen, Paolo Salomoni, Irene Gottlob, Pierluigi Nicotera.   

Abstract

Mutations in the gene encoding FERM domain-containing 7 protein (FRMD7) are recognized as an important cause of X-linked idiopathic infantile nystagmus (IIN). However, the precise role of FRMD7 and its involvement in the pathogenesis of IIN are not understood. In the present study, we have explored the role of FRMD7 in neuronal development. Using in situ hybridization and immunohistochemistry, we reveal that FRMD7 expression is spatially and temporally regulated in both the human and mouse brain during embryonic and fetal development. Furthermore, we show that FRMD7 expression is up-regulated upon retinoic acid (RA)-induced differentiation of mouse neuroblastoma NEURO2A cells, suggesting FRMD7 may play a role in this process. Indeed, we demonstrate, for the first time, that knockdown of FRMD7 during neuronal differentiation results in altered neurite development. Taken together, our data suggest that FRMD7 is involved in multiple aspects of neuronal development, and have direct importance to further understanding the pathogenesis of IIN.

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Year:  2009        PMID: 19892780     DOI: 10.1093/hmg/ddp500

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  32 in total

Review 1.  What we know about the generation of nystagmus and other ocular oscillations: are we closer to identifying therapeutic targets?

Authors:  Rebecca Jane McLean; Irene Gottlob; Frank Antony Proudlock
Journal:  Curr Neurol Neurosci Rep       Date:  2012-06       Impact factor: 5.081

2.  A novel locus for autosomal dominant congenital motor nystagmus mapped to 1q31-q32.2 between D1S2816 and D1S2692.

Authors:  Xueshan Xiao; Shiqiang Li; Xiangming Guo; Qingjiong Zhang
Journal:  Hum Genet       Date:  2011-11-08       Impact factor: 4.132

3.  Retinal microstructures are altered in patients with idiopathic infantile nystagmus.

Authors:  Jinu Han; Taekjune Lee; Jong Bok Lee; Sueng-Han Han
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2017-06-14       Impact factor: 3.117

4.  Stable cell lines of human SH-SY5Y uniformly expressing wild-type or mutant-type FERM domain containing 7 gene.

Authors:  Jiali Pu; Yanfang Mao; Lingjia Xu; Tingting Zheng; Baorong Zhang
Journal:  Exp Ther Med       Date:  2017-07-09       Impact factor: 2.447

5.  Severity of infantile nystagmus syndrome-like ocular motor phenotype is linked to the extent of the underlying optic nerve projection defect in zebrafish belladonna mutant.

Authors:  Sabina P Huber-Reggi; Chien-Cheng Chen; Lea Grimm; Dominik Straumann; Stephan C F Neuhauss; Melody Ying-Yu Huang
Journal:  J Neurosci       Date:  2012-12-12       Impact factor: 6.167

6.  Extraocular muscles in patients with infantile nystagmus: adaptations at the effector level.

Authors:  Kathleen T Berg; David G Hunter; Erick D Bothun; Rosalia Antunes-Foschini; Linda K McLoon
Journal:  Arch Ophthalmol       Date:  2012-03

7.  Salsalate treatment following traumatic brain injury reduces inflammation and promotes a neuroprotective and neurogenic transcriptional response with concomitant functional recovery.

Authors:  Mouna Lagraoui; Gauthaman Sukumar; Joseph R Latoche; Sean K Maynard; Clifton L Dalgard; Brian C Schaefer
Journal:  Brain Behav Immun       Date:  2016-12-07       Impact factor: 7.217

8.  The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.

Authors:  Mervyn G Thomas; Moira Crosier; Susan Lindsay; Anil Kumar; Shery Thomas; Masasuke Araki; Chris J Talbot; Rebecca J McLean; Mylvaganam Surendran; Katie Taylor; Bart P Leroy; Anthony T Moore; David G Hunter; Richard W Hertle; Patrick Tarpey; Andrea Langmann; Susanne Lindner; Martina Brandner; Irene Gottlob
Journal:  Brain       Date:  2011-02-08       Impact factor: 13.501

9.  Novel mutation c.980_983delATTA compound with c.986C>A mutation of the FRMD7 gene in a Chinese family with X-linked idiopathic congenital nystagmus.

Authors:  Feng-wei Song; Bin-bin Chen; Zhao-hui Sun; Li-ping Wu; Su-juan Zhao; Qi Miao; Xia-jing Tang
Journal:  J Zhejiang Univ Sci B       Date:  2013-06       Impact factor: 3.066

10.  A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus.

Authors:  Rachel J Watkins; Rajashree Patil; Benjamin T Goult; Mervyn G Thomas; Irene Gottlob; Sue Shackleton
Journal:  Hum Mol Genet       Date:  2013-02-12       Impact factor: 6.150

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