Literature DB >> 16526919

A novel mutation in EFNB1, probably with a dominant negative effect, underlying craniofrontonasal syndrome.

Vorasuk Shotelersuk1, Pichit Siriwan, Surasawadee Ausavarat.   

Abstract

Craniofrontonasal syndrome (CFNS) is an X-linked disorder whose main clinical manifestations include coronal craniosynostosis and frontonasal dysplasia. Very recently, CFNS was shown to be caused by mutations in EFNB1 encoding ephrin-B1, and 20 mutations have been described. We report a Thai woman with CFNS, in whom a novel mutation was discovered: c.685_686insG, in exon 5 of EFNB1. It is the first insertion and the most 3' point mutation in EFNB1 reported to date. The mutation is expected to result in a truncated ephrin-B1 of 230 amino acids, composed of a nearly complete extracellular part of ephrin-B1 with no transmembrane and cytoplasmic domains. This truncated protein might become a soluble form of the ligand, which previously was shown to be able to bind to receptors, but fail to cluster and to activate them--in other words, acting as a dominant negative protein. Nonetheless, further studies to detect the protein are needed to substantiate the hypothesis.

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Year:  2006        PMID: 16526919     DOI: 10.1597/05-014.1

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  8 in total

1.  Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1.

Authors:  M E P van den Elzen; S R F Twigg; J A C Goos; A J M Hoogeboom; A M W van den Ouweland; A O M Wilkie; I M J Mathijssen
Journal:  Eur J Hum Genet       Date:  2013-11-27       Impact factor: 4.246

2.  A subset of signal transduction pathways is required for hippocampal growth cone collapse induced by ephrin-A5.

Authors:  Xin Yue; Cheryl Dreyfus; Tony Ah-Ng Kong; Renping Zhou
Journal:  Dev Neurobiol       Date:  2008-09-01       Impact factor: 3.964

3.  The impact of CFNS-causing EFNB1 mutations on ephrin-B1 function.

Authors:  Roman Makarov; Bernhard Steiner; Zoran Gucev; Velibor Tasic; Peter Wieacker; Ilse Wieland
Journal:  BMC Med Genet       Date:  2010-06-17       Impact factor: 2.103

Review 4.  Osteoclasts have multiple roles in bone in addition to bone resorption.

Authors:  Brendan F Boyce; Zhenqiang Yao; Lianping Xing
Journal:  Crit Rev Eukaryot Gene Expr       Date:  2009       Impact factor: 1.807

5.  Additional EFNB1 mutations in craniofrontonasal syndrome.

Authors:  Deeann Wallis; Felicitas Lacbawan; Mahim Jain; Vazken M Der Kaloustian; Carlos E Steiner; John B Moeschler; H Wolfgang Losken; Ilkka I Kaitila; Stephen Cantrell; Virginia K Proud; John C Carey; Donald W Day; Dorit Lev; Ahmad S Teebi; Luther K Robinson; H Eugene Hoyme; Nadia Al-Torki; Jacqueline Siegel-Bartelt; John B Mulliken; Nathaniel H Robin; Dolores Saavedra; Elaine H Zackai; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2008-08-01       Impact factor: 2.802

6.  Isolated Sagittal Synostosis in a Boy with Craniofrontonasal Dysplasia and a Novel EFNB1 Mutation.

Authors:  Bharesh K Chauhan; Jacqueline M Hoover; Hannah Scanga; Anagha Medsinge; Georgianne L Arnold; Ken K Nischal
Journal:  Plast Reconstr Surg Glob Open       Date:  2015-07-08

7.  Genome-Wide Association Studies for Comb Traits in Chickens.

Authors:  Manman Shen; Liang Qu; Meng Ma; Taocun Dou; Jian Lu; Jun Guo; Yuping Hu; Guoqiang Yi; Jingwei Yuan; Congjiao Sun; Kehua Wang; Ning Yang
Journal:  PLoS One       Date:  2016-07-18       Impact factor: 3.240

8.  Aberrant cell segregation in the craniofacial primordium and the emergence of facial dysmorphology in craniofrontonasal syndrome.

Authors:  Terren K Niethamer; Teng Teng; Melanie Franco; Yu Xin Du; Christopher J Percival; Jeffrey O Bush
Journal:  PLoS Genet       Date:  2020-02-24       Impact factor: 5.917

  8 in total

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