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1.
Mol Genet Genomics ; 284(4): 273-87, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20697743

RESUMO

Antlers of deer display the fastest and most robust bone development in the animal kingdom. Deposition of the minerals in the cartilage preceding ossification is a specific feature of the developing antler. We have cloned 28 genes which are upregulated in the cartilaginous section (called mineralized cartilage) of the developing ("velvet") antler of red deer stags, compared to their levels in the fetal cartilage. Fifteen of these genes were further characterized by their expression pattern along the tissue zones (i.e., antler mesenchyme, precartilage, cartilage, bone), and by in situ hybridization of the gene activities at the cellular level. Expression dynamics of genes col1A1, col1A2, col3A1, ibsp, mgp, sparc, runx2, and osteocalcin were monitored and compared in the ossified part of the velvet antler and in the skeleton (in ribs and vertebrae). Expression levels of these genes in the ossified part of the velvet antler exceeded the skeletal levels 10-30-fold or more. Gene expression and comparative sequence analyses of cDNAs and the cognate 5' cis-regulatory regions in deer, cattle, and human suggested that the genes runx2 and osx have a master regulatory role. GC-MS metabolite analyses of glucose, phosphate, ethanolamine-phosphate, and hydroxyproline utilizations confirmed the high activity of mineralization genes in governing the flow of the minerals from the skeleton to the antler bone. Gene expression patterns and quantitative metabolite data for the robust bone development in the antler are discussed in an integrated manner. We also discuss the potential implication of our findings on the deer genes in human osteoporosis research.


Assuntos
Cervos/anatomia & histologia , Regulação da Expressão Gênica , Doenças dos Animais/genética , Animais , Chifres de Veado/anatomia & histologia , Chifres de Veado/fisiologia , Calcificação Fisiológica/genética , Cartilagem/anatomia & histologia , Cartilagem/embriologia , Clonagem Molecular , Subunidade alfa 1 de Fator de Ligação ao Core/genética , DNA Complementar/genética , Cervos/embriologia , Cervos/genética , Cervos/crescimento & desenvolvimento , Feminino , Biblioteca Gênica , Humanos , Hibridização In Situ , Íntrons , Masculino , Análise de Sequência com Séries de Oligonucleotídeos , Osteoporose/genética , Gravidez , RNA/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa
2.
Mol Genet Genomics ; 277(3): 237-48, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17131158

RESUMO

Understanding the molecular mechanisms underlying bone development is a fundamental and fascinating problem in developmental biology, with significant medical implications. Here, we have identified the expression patterns for 36 genes that were characteristic or dominant in the consecutive cell differentiation zones (mesenchyme, precartilage, cartilage) of the tip section of the developing velvet antler of red deer Cervus elaphus. Two major functional groups of these genes clearly outlined: six genes linked to high metabolic demand and other five to tumor biology. Our study demonstrates the advantages of the antler as a source of mesenchymal markers, for distinguishing precartilage and cartilage by different gene expression patterns and for identifying genes involved in the robust bone development, a striking feature of the growing antler. Putative roles for "antler" genes that encode alpha-tropomyosine (tpm1), transgelin (tagln), annexin 2 (anxa2), phosphatidylethanolamine-binding protein (pebp) and apolipoprotein D (apoD) in intense but still controlled tissue proliferation are discussed.


Assuntos
Chifres de Veado/crescimento & desenvolvimento , Chifres de Veado/metabolismo , Cervos/crescimento & desenvolvimento , Cervos/genética , Animais , Anexinas/metabolismo , Sequência de Bases , Condrogênese/genética , Clonagem Molecular , DNA Complementar/genética , Cervos/metabolismo , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento , Humanos , Imuno-Histoquímica , Hibridização In Situ , Masculino , Camundongos , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Homologia de Sequência do Ácido Nucleico , Especificidade da Espécie
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