Literature DB >> 17654118

Let's stick together: the role of the Fras1 and Frem proteins in epidermal adhesion.

Kieran Short1, Fenny Wiradjaja, Ian Smyth.   

Abstract

The Fras1 and Frem extracellular matrix proteins play critical roles in epithelial-mesenchymal interaction during embryonic development. Loss of function in humans results in a recessive embryonic blistering disorder called Fraser syndrome. Inactivation of these proteins, or the proteins with which they interact (e.g., Grip1) has also been shown to underlie members of the 'bleb' family of classic mouse mutants which provide a valuable model of Fraser syndrome. Recent studies supporting direct interactions between the Fras1 and Frem proteins, combined with more rigorous elucidation of their developmental regulation, have shed new light on their activity. We summarize the findings to date, bringing new insight into their role in the regulation of epidermal-basement membrane adhesion and organogenesis during development.

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Year:  2007        PMID: 17654118     DOI: 10.1080/15216540701510581

Source DB:  PubMed          Journal:  IUBMB Life        ISSN: 1521-6543            Impact factor:   3.885


  21 in total

Review 1.  Extending the knowledge in histochemistry and cell biology.

Authors:  Wolfgang-Moritz Heupel; Detlev Drenckhahn
Journal:  Histochem Cell Biol       Date:  2009-11-28       Impact factor: 4.304

Review 2.  An active role for basement membrane assembly and modification in tissue sculpting.

Authors:  Meghan A Morrissey; David R Sherwood
Journal:  J Cell Sci       Date:  2015-02-25       Impact factor: 5.285

3.  Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.

Authors:  Tyler F Beck; Danielle Veenma; Oleg A Shchelochkov; Zhiyin Yu; Bum Jun Kim; Hitisha P Zaveri; Yolande van Bever; Sunju Choi; Hannie Douben; Terry K Bertin; Pragna I Patel; Brendan Lee; Dick Tibboel; Annelies de Klein; David W Stockton; Monica J Justice; Daryl A Scott
Journal:  Hum Mol Genet       Date:  2012-12-05       Impact factor: 6.150

4.  Differential localization profile of Fras1/Frem proteins in epithelial basement membranes of newborn and adult mice.

Authors:  E Pavlakis; A K Makrygiannis; R Chiotaki; G Chalepakis
Journal:  Histochem Cell Biol       Date:  2008-06-18       Impact factor: 4.304

5.  Genetic analysis of fin development in zebrafish identifies furin and hemicentin1 as potential novel fraser syndrome disease genes.

Authors:  Thomas J Carney; Natália Martins Feitosa; Carmen Sonntag; Krasimir Slanchev; Johannes Kluger; Daiji Kiyozumi; Jan M Gebauer; Jared Coffin Talbot; Charles B Kimmel; Kiyotoshi Sekiguchi; Raimund Wagener; Heinz Schwarz; Phillip W Ingham; Matthias Hammerschmidt
Journal:  PLoS Genet       Date:  2010-04-15       Impact factor: 5.917

6.  Novel FREM1 mutations expand the phenotypic spectrum associated with Manitoba-oculo-tricho-anal (MOTA) syndrome and bifid nose renal agenesis anorectal malformations (BNAR) syndrome.

Authors:  Jared Nathanson; Daniel T Swarr; Amihood Singer; Mochi Liu; Amy Chinn; Wendy Jones; Jane Hurst; Nahla Khalek; Elaine Zackai; Anne Slavotinek
Journal:  Am J Med Genet A       Date:  2013-02-08       Impact factor: 2.802

7.  FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome.

Authors:  Anas M Alazami; Ranad Shaheen; Fatema Alzahrani; Katie Snape; Anand Saggar; Bernd Brinkmann; Prashant Bavi; Lihadh I Al-Gazali; Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2009-09       Impact factor: 11.025

8.  Syndactyly in a novel Fras1(rdf) mutant results from interruption of signals for interdigital apoptosis.

Authors:  Elizabeth A Hines; Jamie M Verheyden; Amber J Lashua; Sarah C Larson; Kelsey Branchfield; Eric T Domyan; Juan Gao; Julie F Harvey; John C Herriges; Linghan Hu; David J Mcculley; Kurt Throckmorton; Shigetoshi Yokoyama; Akihiro Ikeda; Guoliang Xu; Xin Sun
Journal:  Dev Dyn       Date:  2016-02-24       Impact factor: 3.780

9.  Pharyngeal morphogenesis requires fras1-itga8-dependent epithelial-mesenchymal interaction.

Authors:  Jared Coffin Talbot; James T Nichols; Yi-Lin Yan; Isaac F Leonard; Ruth A BreMiller; Sharon L Amacher; John H Postlethwait; Charles B Kimmel
Journal:  Dev Biol       Date:  2016-06-02       Impact factor: 3.582

10.  Sprouty1 haploinsufficiency prevents renal agenesis in a model of Fraser syndrome.

Authors:  Jolanta E Pitera; Adrian S Woolf; M Albert Basson; Peter J Scambler
Journal:  J Am Soc Nephrol       Date:  2012-10-11       Impact factor: 10.121

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