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  lüll The developmental control of osteoblast-specific gene expression: role of  specific transcription factors and the extracellular matrix environment Franceschi RTCrit Rev Oral Biol Med  1999[]; 10 (1): 40-57Bone formation is a carefully controlled developmental process involving  morphogen-mediated patterning signals that define areas of initial mesenchyme  condensation followed by induction of cell-specific differentiation programs to  produce chondrocytes and osteoblasts. Positional information is conveyed via  gradients of molecules, such as Sonic Hedgehog that are released from cells  within a particular morphogenic field together with region-specific patterns of  hox gene expression. These, in turn, regulate the localized production of bone  morphogenetic proteins and related molecules which initiate chondrocyte- and  osteoblast-specific differentiation programs. Differentiation requires the  initial commitment of mesenchymal stem cells to a given lineage, followed by  induction of tissue-specific patterns of gene expression. Considerable  information about the control of osteoblast-specific gene expression has come  from analysis of the promoter regions of genes encoding proteins like osteocalcin  that are selectively expressed in bone. Both general and tissue-specific  transcription factors control this promoter. Osf2/Cbfa1, the first  osteoblast-specific transcription factor to be identified, is expressed early in  the osteoblast lineage and interacts with specific DNA sequences in the  osteocalcin promoter essential for its selective expression in osteoblasts. The  OSF2/CBFA1 gene is necessary for the development of mineralized tissues, and its  mutation causes the human disease, cleidocranial dysplasia. Committed  osteoprogenitor cells already expressing Osf2/Cbfa1 must synthesize a collagenous  ECM before they will differentiate. A cell:ECM interaction mediated by  integrin-type cell-surface receptors is essential for the induction of  osteocalcin and other osteoblast-related proteins. This interaction stimulates  the binding of Osf2/Cbfa1 to the osteocalcin promoter through an as-yet-undefined  mechanism.|*Gene Expression Regulation, Developmental[MESH]|*Neoplasm Proteins[MESH]|*Osteoblasts/cytology/metabolism/physiology[MESH]|Animals[MESH]|Bone Morphogenetic Proteins/biosynthesis/genetics[MESH]|Cell Differentiation/genetics[MESH]|Cell Lineage[MESH]|Cleidocranial Dysplasia/genetics[MESH]|Core Binding Factor Alpha 1 Subunit[MESH]|Extracellular Matrix/genetics/physiology[MESH]|Genes, Homeobox[MESH]|Humans[MESH]|Integrin-Binding Sialoprotein[MESH]|Osteocalcin/biosynthesis/*genetics[MESH]|Osteogenesis/*genetics[MESH]|Promoter Regions, Genetic[MESH]|Sialoglycoproteins/genetics[MESH]|Transcription Factors/*physiology[MESH] |