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Regulation of the 5'-flanking region of the human CYP27B1 gene in osteoblast cells.
- Source :
-
Molecular and cellular endocrinology [Mol Cell Endocrinol] 2009 Nov 13; Vol. 311 (1-2), pp. 55-61. Date of Electronic Publication: 2009 Jun 11. - Publication Year :
- 2009
-
Abstract
- Synthesis of 1,25-dihydroxyvitamin D(3) (1,25(OH)(2)D(3)) is catalysed by the enzyme 25-hydroxyvitamin D(3)-1alpha-hydroxylase (CYP27B1). Regulation of CYP27B1 gene expression is poorly understood, particularly in non-renal tissues including bone where 1,25(OH)(2)D(3) is hypothesised to serve autocrine/paracrine roles. Transient transfection of ROS 17/2.8 osteoblast-like cells with reporter gene constructs containing deletions of the 5'-flanking region of the human CYP27B1 gene revealed a proximal promoter, enhancer region and strong upstream repressive region. Putative CCAAT and GC boxes, as well as Ets protein binding sites were shown to contribute to promoter and enhancer activities respectively in common with kidney and prostate cells. Inhibition of basal expression was largely attributed to a palindrome 5'-GTCTCAGAC-3' (-1015/-1007bp) that contains two putative canonical Smad binding elements. We conclude that repression of CYP27B1 gene expression may be a common event but the novel inhibitory elements we have identified may be unique to osteoblasts.
- Subjects :
- Animals
Base Sequence
Cell Line, Tumor
DNA Mutational Analysis
Enhancer Elements, Genetic genetics
Humans
Molecular Sequence Data
Osteoblasts drug effects
Promoter Regions, Genetic genetics
Rats
Sequence Deletion
Transforming Growth Factor beta pharmacology
25-Hydroxyvitamin D3 1-alpha-Hydroxylase genetics
5' Flanking Region genetics
Gene Expression Regulation drug effects
Osteoblasts enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1872-8057
- Volume :
- 311
- Issue :
- 1-2
- Database :
- MEDLINE
- Journal :
- Molecular and cellular endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 19524013
- Full Text :
- https://doi.org/10.1016/j.mce.2009.06.001