Literature DB >> 15878328

Identification of a novel cell-adhesive protein spatiotemporally expressed in the basement membrane of mouse developing hair follicle.

Daiji Kiyozumi1, Aki Osada, Nagisa Sugimoto, Charles N Weber, Yuichi Ono, Toshio Imai, Akiko Okada, Kiyotoshi Sekiguchi.   

Abstract

We used PCR-based cDNA subtraction to screen for genes up-regulated during mouse hair morphogenesis. One gene selected was predominantly expressed at the tip of developing hair follicles and encoded a protein characterized by the presence of twelve tandem repeats of approximately 120 amino acids and a novel N-terminal domain containing an Arg-Gly-Asp cell-adhesive motif. Immunohistochemistry demonstrated that the protein encoded by this gene, named QBRICK, was localized at the basement membrane zone of embryonic epidermis and hair follicles, in which it was more enriched at the tip rather than the stalk region. Cell adhesion assays showed that QBRICK was active in mediating cell-substratum adhesion through integrins containing alphav or alpha8 chain, but not integrin alpha5beta1. Immunohistochemistry showed that QBRICK colocalized with alphav-containing integrins in the interfollicular region, but with the alpha8-containing integrin at the tip region of developing hair follicles. These results, together, indicate that QBRICK is an adhesive ligand of basement membrane distinctively recognized by cells in the embryonic skin and hair follicles through different types of integrins directed to the Arg-Gly-Asp motif.

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Year:  2005        PMID: 15878328     DOI: 10.1016/j.yexcr.2005.01.020

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  15 in total

1.  Molecular basis of the recognition of nephronectin by integrin alpha8beta1.

Authors:  Yuya Sato; Toshihiko Uemura; Keisuke Morimitsu; Ryoko Sato-Nishiuchi; Ri-Ichiroh Manabe; Junichi Takagi; Masashi Yamada; Kiyotoshi Sekiguchi
Journal:  J Biol Chem       Date:  2009-04-02       Impact factor: 5.157

2.  Molecular Basis of the Ligand Binding Specificity of αvβ8 Integrin.

Authors:  Akio Ozawa; Yuya Sato; Tsukasa Imabayashi; Toshihiko Uemura; Junichi Takagi; Kiyotoshi Sekiguchi
Journal:  J Biol Chem       Date:  2016-03-31       Impact factor: 5.157

3.  Breakdown of the reciprocal stabilization of QBRICK/Frem1, Fras1, and Frem2 at the basement membrane provokes Fraser syndrome-like defects.

Authors:  Daiji Kiyozumi; Nagisa Sugimoto; Kiyotoshi Sekiguchi
Journal:  Proc Natl Acad Sci U S A       Date:  2006-07-31       Impact factor: 11.205

4.  fras1 shapes endodermal pouch 1 and stabilizes zebrafish pharyngeal skeletal development.

Authors:  Jared Coffin Talbot; Macie B Walker; Thomas J Carney; Tyler R Huycke; Yi-Lin Yan; Ruth A BreMiller; Linda Gai; April Delaurier; John H Postlethwait; Matthias Hammerschmidt; Charles B Kimmel
Journal:  Development       Date:  2012-08       Impact factor: 6.868

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.  A genetic polymorphism of FREM1 is associated with resistance against HIV infection in the Pumwani sex worker cohort.

Authors:  Ma Luo; James Sainsbury; Jeffrey Tuff; Philip A Lacap; Xin-Yong Yuan; Taha Hirbod; Joshua Kimani; Charles Wachihi; Sue Ramdahin; Thomas Bielawny; Joanne Embree; Kristina Broliden; T Blake Ball; Francis A Plummer
Journal:  J Virol       Date:  2012-08-22       Impact factor: 5.103

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.  Basement membrane assembly of the integrin α8β1 ligand nephronectin requires Fraser syndrome-associated proteins.

Authors:  Daiji Kiyozumi; Makiko Takeichi; Itsuko Nakano; Yuya Sato; Tomohiko Fukuda; Kiyotoshi Sekiguchi
Journal:  J Cell Biol       Date:  2012-05-21       Impact factor: 10.539

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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