Literature DB >> 8101169

Expression of the mouse goosecoid gene during mid-embryogenesis may mark mesenchymal cell lineages in the developing head, limbs and body wall.

S J Gaunt1, M Blum, E M De Robertis.   

Abstract

After an earlier, transient phase of expression in the developing primitive streak of 6.4- to 6.8-day mouse embryos, the homeobox gene goosecoid is now shown to be expressed in a later phase of mouse development, from 10.5 days onwards. The later, spatially restricted domains of goosecoid expression are detected in the head, limbs and ventrolateral body wall. At all sites, the domains of expression are first detected in undifferentiated tissue, and then expression persists as these tissues undergo subsequent morphogenesis. For example, goosecoid expression is noted in the first branchial arch at 10.5 days, and then expression persists as this tissue undergoes morphogenesis to form the lower jaw and the body of the tongue. Expression in tissues around the first branchial cleft persists as these undergo morphogenesis to form the base of the auditory meatus and eustachian tube. Expression in tissues around the newly formed nasal pits persists as these elongate to form the nasal chambers. Expression in the ventral epithelial lining of the otic vesicle persists as this eventually gives rise to the non-sensory epithelium of the cochlea. Expression in the proximal limb buds and ventrolateral body wall persists as these tissues undergo morphogenesis to form proximal limb structures and ventral ribs respectively. Our findings lead us to suggest that the goosecoid gene product plays a role in spatial programming within discrete embryonic fields, and possibly lineage compartments, during organogenesis stages of mouse development.

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Year:  1993        PMID: 8101169     DOI: 10.1242/dev.117.2.769

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  15 in total

Review 1.  Evolution and development of teeth.

Authors:  M McCollum; P T Sharpe
Journal:  J Anat       Date:  2001 Jul-Aug       Impact factor: 2.610

2.  The molecular anatomy of mammalian upper lip and primary palate fusion at single cell resolution.

Authors:  Hong Li; Kenneth L Jones; Joan E Hooper; Trevor Williams
Journal:  Development       Date:  2019-06-17       Impact factor: 6.868

3.  Spemann organizer gene Goosecoid promotes delamination of neuroblasts from the otic vesicle.

Authors:  Husniye Kantarci; Andrea Gerberding; Bruce B Riley
Journal:  Proc Natl Acad Sci U S A       Date:  2016-10-19       Impact factor: 11.205

4.  The canonical Wnt signaling activator, R-spondin2, regulates craniofacial patterning and morphogenesis within the branchial arch through ectodermal-mesenchymal interaction.

Authors:  Yong-Ri Jin; Taryn J Turcotte; Alison L Crocker; Xiang Hua Han; Jeong Kyo Yoon
Journal:  Dev Biol       Date:  2011-01-13       Impact factor: 3.582

5.  The mouse goosecoïd gene (Gsc) maps to the telomeric part of mouse chromosome 12.

Authors:  J L Guénet; D Simon-Chazottes; E de Robertis; M Blum
Journal:  Mamm Genome       Date:  1995-11       Impact factor: 2.957

6.  The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development.

Authors:  S Gottlieb; B S Emanuel; D A Driscoll; B Sellinger; Z Wang; B Roe; M L Budarf
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

7.  Positive and negative regulation of the transforming growth factor beta/activin target gene goosecoid by the TFII-I family of transcription factors.

Authors:  Manching Ku; Sergei Y Sokol; Jack Wu; Maria Isabel Tussie-Luna; Ananda L Roy; Akiko Hata
Journal:  Mol Cell Biol       Date:  2005-08       Impact factor: 4.272

8.  Drosophila goosecoid participates in neural development but not in body axis formation.

Authors:  M Hahn; H Jäckle
Journal:  EMBO J       Date:  1996-06-17       Impact factor: 11.598

Review 9.  SAMS, a syndrome of short stature, auditory-canal atresia, mandibular hypoplasia, and skeletal abnormalities is a unique neurocristopathy caused by mutations in Goosecoid.

Authors:  David A Parry; Clare V Logan; Alexander P A Stegmann; Zakia A Abdelhamed; Alistair Calder; Shabana Khan; David T Bonthron; Virginia Clowes; Eamonn Sheridan; Neeti Ghali; Albert E Chudley; Angus Dobbie; Constance T R M Stumpel; Colin A Johnson
Journal:  Am J Hum Genet       Date:  2013-11-27       Impact factor: 11.025

10.  Smad4 is required to regulate the fate of cranial neural crest cells.

Authors:  Seung O Ko; Il Hyuk Chung; Xun Xu; Shoji Oka; Hu Zhao; Eui Sic Cho; Chuxia Deng; Yang Chai
Journal:  Dev Biol       Date:  2007-10-04       Impact factor: 3.582

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