Literature DB >> 16397896

Zic3 is critical for early embryonic patterning during gastrulation.

Stephanie M Ware1, Karine G Harutyunyan, John W Belmont.   

Abstract

Mutations in the zinc finger transcription factor ZIC3 are associated with human left-right patterning abnormalities (X-linked heterotaxy, HTX1, MIM 306955), and mice null for Zic3 show a similar phenotype. However, the developmental function of Zic3 is largely unknown and its expression in early embryonic development suggests a role prior to organ formation. The current study of Zic3 null mice identifies a novel function for Zic3 in the gastrula-stage embryo. Analysis of Zic3 function at early embryonic stages shows that it ensures the fidelity of embryonic patterning, including patterning of the anterior visceral endoderm, the initiation of gastrulation, and positioning of the primitive streak. At later stages, deficiency of Zic3 results in abnormal mesoderm allocation. These results indicate a requirement for Zic3 during early embryogenesis prior to cardiac and visceral organ patterning.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16397896     DOI: 10.1002/dvdy.20668

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  23 in total

1.  An essential and highly conserved role for Zic3 in left-right patterning, gastrulation and convergent extension morphogenesis.

Authors:  Ashley E Cast; Chunlei Gao; Jeffrey D Amack; Stephanie M Ware
Journal:  Dev Biol       Date:  2012-01-21       Impact factor: 3.582

2.  Zic3 is required for maintenance of pluripotency in embryonic stem cells.

Authors:  Linda Shushan Lim; Yuin-Han Loh; Weiwei Zhang; Yixun Li; Xi Chen; Yinan Wang; Manjiri Bakre; Huck-Hui Ng; Lawrence W Stanton
Journal:  Mol Biol Cell       Date:  2007-01-31       Impact factor: 4.138

3.  Genetic and functional analyses of ZIC3 variants in congenital heart disease.

Authors:  Jason Cowan; Muhammad Tariq; Stephanie M Ware
Journal:  Hum Mutat       Date:  2014-01       Impact factor: 4.878

Review 4.  Spectrum of clinical diseases caused by disorders of primary cilia.

Authors:  Stephanie M Ware; Meral Gunay- Aygun; Friedhelm Hildebrandt
Journal:  Proc Am Thorac Soc       Date:  2011-09

5.  Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.

Authors:  Aimee D C Paulussen; Anja Steyls; Jo Vanoevelen; Florence Hj van Tienen; Ingrid P C Krapels; Godelieve Rf Claes; Sonja Chocron; Crool Velter; Gita M Tan-Sindhunata; Catarina Lundin; Irene Valenzuela; Balint Nagy; Iben Bache; Lisa Leth Maroun; Kristiina Avela; Han G Brunner; Hubert J M Smeets; Jeroen Bakkers; Arthur van den Wijngaard
Journal:  Eur J Hum Genet       Date:  2016-07-13       Impact factor: 4.246

6.  A mouse model of conduction system patterning abnormalities in heterotaxy syndrome.

Authors:  Richard J Czosek; Allison Haaning; Stephanie M Ware
Journal:  Pediatr Res       Date:  2010-10       Impact factor: 3.756

7.  Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice.

Authors:  Malgorzata E Quinn; Allison Haaning; Stephanie M Ware
Journal:  Hum Mol Genet       Date:  2012-01-10       Impact factor: 6.150

8.  The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle.

Authors:  Lisa C A D'Alessandro; Brande C Latney; Prasuna C Paluru; Elizabeth Goldmuntz
Journal:  Am J Med Genet A       Date:  2013-02-20       Impact factor: 2.802

Review 9.  The ZIC gene family encodes multi-functional proteins essential for patterning and morphogenesis.

Authors:  Rob Houtmeyers; Jacob Souopgui; Sabine Tejpar; Ruth Arkell
Journal:  Cell Mol Life Sci       Date:  2013-02-27       Impact factor: 9.261

10.  MicroRNA-155 is an Epstein-Barr virus-induced gene that modulates Epstein-Barr virus-regulated gene expression pathways.

Authors:  Qinyan Yin; Jane McBride; Claire Fewell; Michelle Lacey; Xia Wang; Zhen Lin; Jennifer Cameron; Erik K Flemington
Journal:  J Virol       Date:  2008-03-26       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.