Literature DB >> 8288580

The mouse osteocalcin gene cluster contains three genes with two separate spatial and temporal patterns of expression.

C Desbois1, D A Hogue, G Karsenty.   

Abstract

Osteocalcin is the most abundant noncollagenous protein of bone. Here we report that the mouse genome contains an osteocalcin cluster composed of three genes arranged within a 23-kilobase span of genomic DNA. We named them osteocalcin gene 1 (OG1), osteocalcin gene 2 (OG2), and osteocalcin-related gene (ORG) in order from the 5' end to the 3' end of the cluster. Hybridization of polymerase chain reaction-amplified cDNAs with specific oligonucleotides and RNase protection assays showed that OG1 and OG2 are expressed only in bone, whereas ORG is transcribed in kidney but not in bone. Furthermore, during embryogenesis, OG1 and OG2 begin to be expressed at day 15.5, while ORG is transcribed as early as day 10.5. The protein encoded by ORG has a similar pattern of expression and identical structural features to nephrocalcin, a calcium-binding protein partially purified from kidney that plays a role in calcium reabsorption and in prevention of nephrolithiasis. The nephrocalcin gene has not been cloned in any species; we propose that ORG is the mouse nephrocalcin gene. The existence of several osteocalcin or osteocalcin-related sequences is not restricted to mouse but is present in every species we examined.

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Year:  1994        PMID: 8288580

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  52 in total

1.  Osteoblast-specific gene expression after transplantation of marrow cells: implications for skeletal gene therapy.

Authors:  Z Hou; Q Nguyen; B Frenkel; S K Nilsson; M Milne; A J van Wijnen; J L Stein; P Quesenberry; J B Lian; G S Stein
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-22       Impact factor: 11.205

2.  Osteocyte control of bone formation via sclerostin, a novel BMP antagonist.

Authors:  David G Winkler; May Kung Sutherland; James C Geoghegan; Changpu Yu; Trenton Hayes; John E Skonier; Diana Shpektor; Mechtild Jonas; Brian R Kovacevich; Karen Staehling-Hampton; Mark Appleby; Mary E Brunkow; John A Latham
Journal:  EMBO J       Date:  2003-12-01       Impact factor: 11.598

3.  Chondrocytes derived from mouse embryonic stem cells.

Authors:  Jan Kramer; Claudia Hegert; Gunnar Hargus; Jürgen Rohwedel
Journal:  Cytotechnology       Date:  2003-03       Impact factor: 2.058

4.  Brachy-syndactyly caused by loss of Sfrp2 function.

Authors:  Roy Morello; Terry K Bertin; Silke Schlaubitz; Chad A Shaw; Sujatha Kakuru; Elda Munivez; Pia Hermanns; Yuqing Chen; Bernhard Zabel; Brendan Lee
Journal:  J Cell Physiol       Date:  2008-10       Impact factor: 6.384

5.  Parathyroid hormone-related protein induces spontaneous osteoclast formation via a paracrine cascade.

Authors:  I A Nakchbandi; E E Weir; K L Insogna; W M Philbrick; A E Broadus
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

6.  Identification of a gene that reverses the immortal phenotype of a subset of cells and is a member of a novel family of transcription factor-like genes.

Authors:  M J Bertram; N G Bérubé; X Hang-Swanson; Q Ran; J K Leung; S Bryce; K Spurgers; R J Bick; A Baldini; Y Ning; L J Clark; E K Parkinson; J C Barrett; J R Smith; O M Pereira-Smith
Journal:  Mol Cell Biol       Date:  1999-02       Impact factor: 4.272

7.  The skeleton gets a (reproductive) life.

Authors:  Charles M Allan; David J Handelsman
Journal:  Asian J Androl       Date:  2011-06-06       Impact factor: 3.285

Review 8.  Tissue specific and vitamin D responsive gene expression in bone.

Authors:  C White; E Gardiner; J Eisman
Journal:  Mol Biol Rep       Date:  1998-01       Impact factor: 2.316

9.  Progressive recruitment of Runx2 to genomic targets despite decreasing expression during osteoblast differentiation.

Authors:  Steven Pregizer; Sanjeev K Baniwal; Xiting Yan; Zea Borok; Baruch Frenkel
Journal:  J Cell Biochem       Date:  2008-11-01       Impact factor: 4.429

10.  Hind limb unloading of mice modulates gene expression at the protein and mRNA level in mesenchymal bone cells.

Authors:  Davide Visigalli; Antonella Strangio; Daniela Palmieri; Paola Manduca
Journal:  BMC Musculoskelet Disord       Date:  2010-07-05       Impact factor: 2.362

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