Abstract

Bone sialoprotein is a 70-kDa extracellular matrix component that is intimately associated with biomineralization, yet the cis-acting elements of the Bsp gene that restrict its expression to mineralizing cells remain uncharacterized. To identify such elements, we analyzed a 2472-base pair fragment of the murine promoter that directs osteoblast-selective expression of a luciferase reporter gene and found that the region between -338 and -178 relative to the transcriptional start is crucial for its osteoblast-selective activity. We identified an element within this region that binds a protein complex in the nuclear extracts of osteoblastic cells and is required for its transcriptional activity. Introduction of a mutation that disrupts a homeodomain binding site within this sequence eliminates both its in vitro binding and nearly all of the osteoblastic-selective activity of the 2472-base pair promoter. We further found that the Dlx5 homeoprotein, which is able to regulate the osteoblast-specific osteocalcin promoter, can bind this element and stimulate its enhancer activity when overexpressed in COS7 cells. These data represent the first description of an osteoblast-specific element within the bone sialoprotein promoter and demonstrate its regulation by a member of a family of factors known to be involved in skeletogenesis.

Highlights

  • Bone sialoprotein (BSP)1 is a 70-kDa extracellular matrix component that is selectively produced by mineralizing cell types in a pattern that correlates with the onset of mineral formation in vivo

  • ROS 17/2.8 osteosarcoma cells, which express high levels of osteocalcin but not of BSP (Fig. 1C), exhibited only 20% of the luciferase activity seen in clone 4 cells when transfected with the p2472 construct, comparable to those seen in C2C12 myoblasts and 3T3-L1 preadipocytes, two mesenchymal cell lines that do not express BSP (Fig. 1D)

  • The 2472-bp murine Bsp promoter is expressed at high levels only in cells that produce BSP and in a pattern that mirrors that of the endogenous message

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Summary

Osteoblast Specificity of the Mouse Bsp Promoter

Quences have so far been unsuccessful, we took the alternate approach of conducting a systematic study of the 2472-bp promoter to identify osteoblast-specific elements. This study has revealed that a homeodomain binding site in the proximal promoter is required for the tissue-specific expression of the murine Bsp gene. This site is positively regulated by the Dlx homeoprotein, which is known to play an important role in skeletogenesis

EXPERIMENTAL PROCEDURES
RESULTS
TATGGATCCCTCTAACTACCATCTTCTCC TATGGATCCCAAGCCTCTTGGCAGAAGG
DISCUSSION
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