Literature DB >> 9426254

Molecular cloning, chromosomal mapping and developmental expression of BAPX1, a novel human homeobox-containing gene homologous to Drosophila bagpipe.

C Tribioli1, T Lufkin.   

Abstract

We describe here the cloning of the human BAPX1 gene, a homologue of the Drosophila bagpipe gene which has 87% aa identity within the homeodomain relative to the fly gene. We recently have identified the murine bagpipe homolog. The predicted aa sequence of the human gene has 85% overall identity to the murine gene, with 100% identity in the homeodomain. In mouse, this gene maps to the proximal portion of chromosome 5. We show that the human gene maps to 4p16.1, the human region syntenic with mouse chromosome 5. Expression of BAPX1 was evaluated during human embryonic development by RT-PCR analysis and by RNA in situ hybridization. RT-PCR analysis showed that BAPX1 is expressed in embryo tissues, particularly the limb, and at a lower level in an embryonic lung cell line. RNA in situ hybridization revealed that BAPX1 is predominantly expressed in mesenchymal condensations of the fetal limb and axial skeleton, and in lateral plate mesoderm giving rise to visceral muscle. The expression pattern of BAPX1 combined with the chromosomal localization to 4p16.1, where several human genetic diseases involving dysmorphology of the skeleton have been assigned, raises the potential of it being a candidate gene for one of these disorders. O

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Year:  1997        PMID: 9426254     DOI: 10.1016/s0378-1119(97)00520-9

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  12 in total

1.  The mouse bagpipe gene controls development of axial skeleton, skull, and spleen.

Authors:  L A Lettice; L A Purdie; G J Carlson; F Kilanowski; J Dorin; R E Hill
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-17       Impact factor: 11.205

Review 2.  The role of Bapx1 (Nkx3.2) in the development and evolution of the axial skeleton.

Authors:  L Lettice; J Hecksher-Sørensen; R Hill
Journal:  J Anat       Date:  2001 Jul-Aug       Impact factor: 2.610

3.  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

4.  Pbx1/Pbx2 govern axial skeletal development by controlling Polycomb and Hox in mesoderm and Pax1/Pax9 in sclerotome.

Authors:  Terence D Capellini; Rediet Zewdu; Giuseppina Di Giacomo; Stefania Asciutti; Jamie E Kugler; Anna Di Gregorio; Licia Selleri
Journal:  Dev Biol       Date:  2008-04-16       Impact factor: 3.582

5.  A quantitative and qualitative RNA expression profiling assay for cell culture with single cell resolution.

Authors:  Petra Kraus; Rachel Yerden; Darren Sipes; Shantanu Sur; Thomas Lufkin
Journal:  Cytotechnology       Date:  2017-08-10       Impact factor: 2.058

6.  A role for FoxN3 in the development of cranial cartilages and muscles in Xenopus laevis (Amphibia: Anura: Pipidae) with special emphasis on the novel rostral cartilages.

Authors:  Jennifer Schmidt; Maximilian Schuff; Lennart Olsson
Journal:  J Anat       Date:  2010-11-03       Impact factor: 2.610

Review 7.  Genetic Advances in the Understanding of Microtia.

Authors:  Craig Gendron; Ann Schwentker; John A van Aalst
Journal:  J Pediatr Genet       Date:  2016-09-23

8.  Exogenous signal-independent nuclear IkappaB kinase activation triggered by Nkx3.2 enables constitutive nuclear degradation of IkappaB-alpha in chondrocytes.

Authors:  Yeryoung Yong; Seung-Won Choi; Hye-Jeong Choi; Hyung Wook Nam; Jeong-Ah Kim; Da-Un Jeong; Don Young Kim; Yu Sam Kim; Dae-Won Kim
Journal:  Mol Cell Biol       Date:  2011-05-23       Impact factor: 4.272

9.  The role of Nkx3.2 in chondrogenesis.

Authors:  Roshni S Rainbow; Heenam K Won; Li Zeng
Journal:  Front Biol (Beijing)       Date:  2014-07-07

10.  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

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