Literature DB >> 11702952

The chick transcriptional repressor Nkx3.2 acts downstream of Shh to promote BMP-dependent axial chondrogenesis.

L C Murtaugh1, L Zeng, J H Chyung, A B Lassar.   

Abstract

Previously, we demonstrated that Shh acts early in the development of the axial skeleton, to induce a prochondrogenic response to later BMP signaling. Here, we demonstrate that somitic expression of the transcription factor Nkx3.2 is initiated by Shh and sustained by BMP signals. Misexpression of Nkx3.2 in somitic tissue confers a prochondrogenic response to BMP signals. The transcriptional repressor activity of Nkx3.2 is essential for this factor to promote chondrogenesis. Conversely, a "reverse function" mutant of Nkx3.2 that has been converted into a transcriptional activator inhibits axial chondrogenesis in vivo. We conclude that Nkx3.2 is a critical mediator of the actions of Shh during axial cartilage formation, acting to inhibit expression of factors that interfere with the prochondrogenic effects of BMPs.

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Year:  2001        PMID: 11702952     DOI: 10.1016/s1534-5807(01)00039-9

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  45 in total

Review 1.  Hdac-mediated control of endochondral and intramembranous ossification.

Authors:  Elizabeth W Bradley; Meghan E McGee-Lawrence; Jennifer J Westendorf
Journal:  Crit Rev Eukaryot Gene Expr       Date:  2011       Impact factor: 1.807

2.  Shh establishes an Nkx3.2/Sox9 autoregulatory loop that is maintained by BMP signals to induce somitic chondrogenesis.

Authors:  Li Zeng; Hervé Kempf; L Charles Murtaugh; Mie Elissa Sato; Andrew B Lassar
Journal:  Genes Dev       Date:  2002-08-01       Impact factor: 11.361

3.  Undulated short-tail deletion mutation in the mouse ablates Pax1 and leads to ectopic activation of neighboring Nkx2-2 in domains that normally express Pax1.

Authors:  Chikara Kokubu; Bettina Wilm; Tomoko Kokubu; Matthias Wahl; Isabel Rodrigo; Norio Sakai; Fabio Santagati; Yoshihide Hayashizaki; Misao Suzuki; Ken-Ichi Yamamura; Kuniya Abe; Kenji Imai
Journal:  Genetics       Date:  2003-09       Impact factor: 4.562

4.  Meox homeodomain proteins are required for Bapx1 expression in the sclerotome and activate its transcription by direct binding to its promoter.

Authors:  Isabel Rodrigo; Paola Bovolenta; Baljinder S Mankoo; Kenji Imai
Journal:  Mol Cell Biol       Date:  2004-04       Impact factor: 4.272

5.  Indian Hedgehog signalling triggers Nkx3.2 protein degradation during chondrocyte maturation.

Authors:  Seung-Won Choi; Da-Un Jeong; Jeong-Ah Kim; Boyoung Lee; Kyu Sang Joeng; Fanxin Long; Dae-Won Kim
Journal:  Biochem J       Date:  2012-05-01       Impact factor: 3.857

Review 6.  Histone Deacetylases in Bone Development and Skeletal Disorders.

Authors:  Elizabeth W Bradley; Lomeli R Carpio; Andre J van Wijnen; Meghan E McGee-Lawrence; Jennifer J Westendorf
Journal:  Physiol Rev       Date:  2015-10       Impact factor: 37.312

7.  Dicer-dependent pathways regulate chondrocyte proliferation and differentiation.

Authors:  Tatsuya Kobayashi; Jun Lu; Bradley S Cobb; Stephen J Rodda; Andrew P McMahon; Ernestina Schipani; Matthias Merkenschlager; Henry M Kronenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2008-01-31       Impact factor: 11.205

8.  Maintenance of the BMP4-dependent stress erythropoiesis pathway in the murine spleen requires hedgehog signaling.

Authors:  John M Perry; Omid F Harandi; Prashanth Porayette; Shailaja Hegde; Arun K Kannan; Robert F Paulson
Journal:  Blood       Date:  2008-10-16       Impact factor: 22.113

9.  Homozygous inactivating mutations in the NKX3-2 gene result in spondylo-megaepiphyseal-metaphyseal dysplasia.

Authors:  Jan Hellemans; Marleen Simon; Annelies Dheedene; Yasemin Alanay; Ercan Mihci; Laila Rifai; Abdelaziz Sefiani; Yolande van Bever; Morteza Meradji; Andrea Superti-Furga; Geert Mortier
Journal:  Am J Hum Genet       Date:  2009-12       Impact factor: 11.025

10.  The transcriptional cofactor Lbh regulates angiogenesis and endochondral bone formation during fetal bone development.

Authors:  K L Conen; S Nishimori; S Provot; H M Kronenberg
Journal:  Dev Biol       Date:  2009-07-14       Impact factor: 3.582

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