Literature DB >> 10704861

Expression patterns of Twist and Fgfr1, -2 and -3 in the developing mouse coronal suture suggest a key role for twist in suture initiation and biogenesis.

D Johnson1, S Iseki, A O Wilkie, G M Morriss-Kay.   

Abstract

Sutural growth depends on maintenance of a balance between proliferation of osteogenic stem cells and their differentiation to form new bone, so that the stem cell population is maintained until growth of the skull is complete. The identification of heterozygous mutations in FGFR1, -2 and -3 and TWIST as well as microdeletions of TWIST in human craniosynostosis syndromes has highlighted these genes as playing important roles in maintaining the suture as a growth centre. In contrast to Drosophila, a molecular relationship between human (or other vertebrate) TWIST and FGFR genes has not yet been established. TWIST mutations exert their effect via haploinsufficiency whereas FGFR mutations have a gain-of-function mechanism of action. To investigate the biological basis of FGFR signalling pathways in the developing calvarium we compared the expression patterns of Twist with those of Fgfr1, -2 and -3 in the fetal mouse coronal suture over the course of embryonic days 14-18, as the suture is initiated and matures. Our results show that: (1) Twist expression precedes that of Fgfr genes at the time of initiation of the coronal suture; (2) in contrast to Fgfr transcripts, which are localised within and around the developing bone domains, Twist is expressed by the midsutural mesenchyme cells. Twist expression domains show some overlap with those of Fgfr2, which is expressed in the most immature (proliferating) osteogenic tissue.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10704861     DOI: 10.1016/s0925-4773(99)00278-6

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  32 in total

Review 1.  Derivation of the mammalian skull vault.

Authors:  G M Morriss-Kay
Journal:  J Anat       Date:  2001 Jul-Aug       Impact factor: 2.610

2.  A TWIST in the fate of human osteoblasts identifies signaling molecules involved in skull development.

Authors:  E W Jabs
Journal:  J Clin Invest       Date:  2001-05       Impact factor: 14.808

3.  Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome.

Authors:  Greg Holmes; Claudio Basilico
Journal:  Dev Biol       Date:  2012-06-01       Impact factor: 3.582

4.  A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes.

Authors:  M K Hajihosseini; S Wilson; L De Moerlooze; C Dickson
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-27       Impact factor: 11.205

5.  Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation.

Authors:  Ileana Antonopoulou; Lampros A Mavrogiannis; Andrew O M Wilkie; Gillian M Morriss-Kay
Journal:  J Anat       Date:  2004-06       Impact factor: 2.610

Review 6.  Pathology in metopic synostosis.

Authors:  Pinar Karabagli
Journal:  Childs Nerv Syst       Date:  2013-10-03       Impact factor: 1.475

7.  FGF9 monomer-dimer equilibrium regulates extracellular matrix affinity and tissue diffusion.

Authors:  Masayo Harada; Hirotaka Murakami; Akihiko Okawa; Noriaki Okimoto; Shuichi Hiraoka; Taka Nakahara; Ryogo Akasaka; Yo-Ichi Shiraishi; Noriyuki Futatsugi; Yoko Mizutani-Koseki; Atsushi Kuroiwa; Mikako Shirouzu; Shigeyuki Yokoyama; Makoto Taiji; Sachiko Iseki; David M Ornitz; Haruhiko Koseki
Journal:  Nat Genet       Date:  2009-02-15       Impact factor: 38.330

8.  Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice.

Authors:  Yingli Wang; Miao Sun; Victoria L Uhlhorn; Xueyan Zhou; Inga Peter; Neus Martinez-Abadias; Cheryl A Hill; Christopher J Percival; Joan T Richtsmeier; David L Huso; Ethylin Wang Jabs
Journal:  BMC Dev Biol       Date:  2010-02-22       Impact factor: 1.978

9.  Scalp fibroblasts have a shared expression profile in monogenic craniosynostosis.

Authors:  Elena G Bochukova; Shamit Soneji; Steven A Wall; Andrew O M Wilkie
Journal:  J Med Genet       Date:  2009-09-15       Impact factor: 6.318

10.  Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology.

Authors:  Greg Holmes; Gerson Rothschild; Upal Basu Roy; Chu-Xia Deng; Alka Mansukhani; Claudio Basilico
Journal:  Dev Biol       Date:  2009-01-29       Impact factor: 3.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.