Literature DB >> 15736267

XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis.

Paris Ataliotis1, Sarah Ivins, Timothy J Mohun, Peter J Scambler.   

Abstract

The development of pharyngeal arch derivatives in mouse and zebrafish embryos depends on the activity of the transcription factor Tbx1. We cloned the Xenopus laevis orthologue of Tbx1 (XTbx1) and show that the pattern of expression is similar to that in other vertebrate species. Zygotic transcripts are first detected shortly after the mid-blastula transition and are localized to the presumptive mesoderm at mid-gastrula stages. XTbx1 expression persists in the lateral plate mesoderm at neurula stages and is found in the pharyngeal arches and otic vesicles from early tail bud stages onward. We demonstrate that XTbx1 is a transcriptional activator and that this trans-activation requires the C-terminal region of the protein. A dominant interfering mutant of XTbx1 disrupts the development of Xenopus head structures and pharyngeal arch derivatives. Lineage labeling reveals a requirement for XTbx1 function in cells that contribute to the pharyngeal mesoderm and for fgf8 expression. Copyright 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15736267     DOI: 10.1002/dvdy.20276

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


  24 in total

Review 1.  How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease.

Authors:  Alvin J Chin; Jean-Pierre Saint-Jeannet; Cecilia W Lo
Journal:  Mech Dev       Date:  2012-05-26       Impact factor: 1.882

2.  Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.

Authors:  Katrina Prescott; Sarah Ivins; Mike Hubank; Elizabeth Lindsay; Antonio Baldini; Peter Scambler
Journal:  Hum Genet       Date:  2005-03-19       Impact factor: 4.132

3.  Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development.

Authors:  Zhen Zhang; Tuong Huynh; Antonio Baldini
Journal:  Development       Date:  2006-08-16       Impact factor: 6.868

4.  Identification and developmental expression of two Tbx1/10-related genes in the agnathan Lethenteron japonicum.

Authors:  Eva Tiecke; Manami Matsuura; Nobuhiro Kokubo; Shigehiro Kuraku; Rie Kusakabe; Shigeru Kuratani; Mikiko Tanaka
Journal:  Dev Genes Evol       Date:  2007-09-15       Impact factor: 0.900

5.  An interspecies heart-to-heart: Using Xenopus to uncover the genetic basis of congenital heart disease.

Authors:  Alexandra MacColl Garfinkel; Mustafa K Khokha
Journal:  Curr Pathobiol Rep       Date:  2017-05-06

6.  Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.

Authors:  Richard Paylor; Beate Glaser; Annalisa Mupo; Paris Ataliotis; Corinne Spencer; Angela Sobotka; Chelsey Sparks; Chul-Hee Choi; John Oghalai; Sarah Curran; Kieran C Murphy; Stephen Monks; Nigel Williams; Michael C O'Donovan; Michael J Owen; Peter J Scambler; Elizabeth Lindsay
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-09       Impact factor: 11.205

Review 7.  22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development.

Authors:  Peter J Scambler
Journal:  Pediatr Cardiol       Date:  2010-04       Impact factor: 1.655

8.  Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome.

Authors:  Kelly Lammerts van Bueren; Irinna Papangeli; Francesca Rochais; Kerra Pearce; Catherine Roberts; Amelie Calmont; Dorota Szumska; Robert G Kelly; Shoumo Bhattacharya; Peter J Scambler
Journal:  Dev Biol       Date:  2010-02-01       Impact factor: 3.582

9.  Tbx1 regulates the BMP-Smad1 pathway in a transcription independent manner.

Authors:  F Gabriella Fulcoli; Tuong Huynh; Peter J Scambler; Antonio Baldini
Journal:  PLoS One       Date:  2009-06-25       Impact factor: 3.240

10.  EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis.

Authors:  Youe Li; Jose M Manaligod; Daniel L Weeks
Journal:  Biol Cell       Date:  2010-02-17       Impact factor: 4.458

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