Mackey S L, Heymont J L, Kronenberg H M, Demay M B
Endocrine Units, Massachusetts General Hospital, Harvard Medical School, Boston, USA.
Mol Endocrinol. 1996 Mar;10(3):298-305. doi: 10.1210/mend.10.3.8833658.
An important physiological control of PTH gene expression is its transcriptional repression by 1,25-dihydroxyvitamin D(3) [1,25-(OH)(2)D(3)]. The mechanism of this 1,25-(OH)(2)D(3)-mediated transcriptional repression is poorly understood. Previous investigations have identified a DNA sequence in the 5'-regulatory region of the human PTH (hPTH) gene that binds the vitamin D receptor (VDR) and mediates transcription repression in response to 1,25(OH)(2)D(3) in GH4CI cells. The hPTH gene sequence does not mediate transcriptional repression in ROS 17/2.8 cells, even though up-regulatory vitamin D response elements (VDREs) are active in these cells. The hPTH DNA sequence differs from the upregulatory VDREs in that it contains a single copy of a hexameric motif (AGGUC) homologous to those repeated in the up-regulatory VDREs. The protein-DNA interactions of this sequence were examined using nuclear extracts from bovine parathyroid, GH4CI, and ROS 17/2.8 cells. In bovine parathyroid nuclear extracts, the VDR binds the down-regulatory hPTH DNA sequence independently of the retinoid X receptor (RXR). In GH4C1 nuclear extracts, two VDR-containing complexes are observed: one lacking RXR and one containing RXR. In ROS 17/2.8 nuclear extracts, a single VDRdependent complex containing RXR is observed. When the up-regulatory rat osteocalcin VDRE is used as a probe, only VDR-RXR-containing complexes are generated using nuclear extracts from all three cell types. These results demonstrate that the sequence that mediates transcriptional repression in response to 1 ,25-(OH)(2)D(3) differs from the up-regulatory response elements both in sequence composition and in its ability to bind VDR independently of RXR.
甲状旁腺激素(PTH)基因表达的一个重要生理调控是其受1,25 - 二羟维生素D(3)[1,25 - (OH)(2)D(3)]的转录抑制。这种1,25 - (OH)(2)D(3)介导的转录抑制机制尚不清楚。先前的研究在人PTH(hPTH)基因的5' - 调控区鉴定出一个DNA序列,该序列可结合维生素D受体(VDR)并在GH4CI细胞中介导对1,25(OH)(2)D(3)的转录抑制。尽管上调性维生素D反应元件(VDREs)在ROS 17/2.8细胞中具有活性,但hPTH基因序列在这些细胞中并不介导转录抑制。hPTH DNA序列与上调性VDREs的不同之处在于它含有一个六聚体基序(AGGUC)的单拷贝,该基序与上调性VDREs中重复的基序同源。使用来自牛甲状旁腺、GH4CI和ROS 17/2.8细胞的核提取物检查了该序列的蛋白质 - DNA相互作用。在牛甲状旁腺核提取物中,VDR独立于视黄酸X受体(RXR)结合下调性hPTH DNA序列。在GH4C1核提取物中,观察到两种含VDR的复合物:一种缺乏RXR,一种含有RXR。在ROS 17/2.8核提取物中,观察到一种单一的含VDR和RXR的复合物。当使用上调性大鼠骨钙素VDRE作为探针时,使用来自所有三种细胞类型的核提取物仅产生含VDR - RXR的复合物。这些结果表明,介导对1,25 - (OH)(2)D(3)转录抑制的序列在序列组成以及独立于RXR结合VDR的能力方面均与上调性反应元件不同。