Literature DB >> 12464437

The mouse rib-vertebrae mutation is a hypomorphic Tbx6 allele.

Masami Watabe-Rudolph1, Nicole Schlautmann, Virginia E Papaioannou, Achim Gossler.   

Abstract

Rib-vertebrae (rv) is an autosomal recessive mutation in mouse that affects somite formation, morphology, and patterning. Expression of Notch pathway components is affected in the paraxial mesoderm of rv mutant embryos, and rv and a null allele of the Notch ligand delta1 show non-allelic non-complementation. By fine genetic mapping and complementation testing we have identified Tbx6, a gene essential for paraxial mesoderm formation, as the gene mutated in rv. Compound heterozygotes carrying a Tbx6 null allele and rv show a phenotype that is milder than in homozygous Tbx6 null but more severe than in homozygous rv mutants. Tbx6 expression is down-regulated in rv mutant embryos. An insertion in the promoter region upstream of the transcriptional start is present in the genome of rv mutants but not in different strains of mice wild type for Tbx6. Our results indicate that rv is a regulatory mutation of Tbx6 causing a hypomorphic phenotype.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12464437     DOI: 10.1016/s0925-4773(02)00394-5

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


  27 in total

Review 1.  T-box genes in early embryogenesis.

Authors:  Chris Showell; Olav Binder; Frank L Conlon
Journal:  Dev Dyn       Date:  2004-01       Impact factor: 3.780

2.  Analysis of TBX18 expression in chick embryos.

Authors:  Bénédicte Haenig; Andreas Kispert
Journal:  Dev Genes Evol       Date:  2004-07-15       Impact factor: 0.900

3.  WNT signaling, in synergy with T/TBX6, controls Notch signaling by regulating Dll1 expression in the presomitic mesoderm of mouse embryos.

Authors:  Michael Hofmann; Karin Schuster-Gossler; Masami Watabe-Rudolph; Alexander Aulehla; Bernhard G Herrmann; Achim Gossler
Journal:  Genes Dev       Date:  2004-11-15       Impact factor: 11.361

4.  Paraxial mesoderm contributes stromal cells to the developing kidney.

Authors:  Richard Guillaume; Michel Bressan; Doris Herzlinger
Journal:  Dev Biol       Date:  2009-03-06       Impact factor: 3.582

5.  A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse.

Authors:  Isabel Rubio-Aliaga; Dian Soewarto; Sibylle Wagner; Matthias Klaften; Helmut Fuchs; Svetoslav Kalaydjiev; Dirk H Busch; Martina Klempt; Birgit Rathkolb; Eckhard Wolf; Koichiro Abe; Stefan Zeiser; Gerhard K H Przemeck; Johannes Beckers; Martin Hrabé de Angelis
Journal:  Genetics       Date:  2006-12-18       Impact factor: 4.562

6.  TBX6 null variants and a common hypomorphic allele in congenital scoliosis.

Authors:  N Wu; X Ming; J Xiao; Z Wu; X Chen; M Shinawi; Y Shen; G Yu; J Liu; H Xie; Z S Gucev; S Liu; N Yang; H Al-Kateb; J Chen; J Zhang; N Hauser; T Zhang; V Tasic; P Liu; X Su; X Pan; C Liu; L Wang; J Shen; J Shen; Y Chen; T Zhang; J Zhang; K W Choy; J Wang; Q Wang; S Li; W Zhou; J Guo; Y Wang; C Zhang; Hong Zhao; Yu An; Yu Zhao; J Wang; Z Liu; Y Zuo; Y Tian; X Weng; V R Sutton; H Wang; Y Ming; S Kulkarni; T P Zhong; P F Giampietro; S L Dunwoodie; S W Cheung; X Zhang; L Jin; J R Lupski; G Qiu; F Zhang
Journal:  N Engl J Med       Date:  2015-01-07       Impact factor: 91.245

Review 7.  Patterning spinal nerves and vertebral bones.

Authors:  Roger Keynes
Journal:  J Anat       Date:  2017-10-24       Impact factor: 2.610

8.  tbx6l and tbx16 are redundantly required for posterior paraxial mesoderm formation during zebrafish embryogenesis.

Authors:  Zachary T Morrow; Adrienne M Maxwell; Kazuyuki Hoshijima; Jared C Talbot; David J Grunwald; Sharon L Amacher
Journal:  Dev Dyn       Date:  2017-08-30       Impact factor: 3.780

Review 9.  The mouse notches up another success: understanding the causes of human vertebral malformation.

Authors:  Duncan B Sparrow; Gavin Chapman; Sally L Dunwoodie
Journal:  Mamm Genome       Date:  2011-06-11       Impact factor: 2.957

10.  Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome.

Authors:  Nan Yang; Nan Wu; Shuangshuang Dong; Ling Zhang; Yanxue Zhao; Weisheng Chen; Renqian Du; Chengcheng Song; Xiaojun Ren; Jiaqi Liu; Davut Pehlivan; Zhenlei Liu; Jia Rao; Chunyan Wang; Sen Zhao; Amy M Breman; Huadan Xue; Hao Sun; Jianxiong Shen; Shuyang Zhang; Jennifer E Posey; Hong Xu; Li Jin; Jianguo Zhang; Pengfei Liu; Simone Sanna-Cherchi; Guixing Qiu; Zhihong Wu; James R Lupski; Feng Zhang
Journal:  Kidney Int       Date:  2020-05-22       Impact factor: 10.612

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.