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Important measures in vitamin D mediated transcriptional regulation involve 1) binding of vitamin D on its cognate vitamin D receptor (VDR), 2) the translocation of vitamin D receptor (VDR)-retinoid X receptor heterodimer advanced in the nucleus, 3) binding VDR-RXR complex on the TRPV6 gene promoter, 4) recruitment of steroid receptor coactivator one and RNA polymerase II on the promoter, and 5) transcriptional activation mediated through histone H4 acetylation activities. Calcium inflow from the diet regime and its subsequent binding to calbindin-D9k could be the rate-restricting stage that modulates vitamin D-dependent regulation TRPV6. At least 5 vitamin D reaction elements (VDREs) at positions −1.2, −2.1, −3.5, −4.3, and −5.5 kb relative to transcriptional commence web site (TSS) have been discovered on TRPV6 transcripts. Among these 5 web sites, VDREs at positions −1.2, −2.1, and −4.3 kb are appreciably more responsive to 1,25-(OH)2D3 in comparison to VDREs located at −3.5 and −5.5 kb which do not seem to lead substantially to vitamin D mediated transcriptional regulation in the intestine. Estrogen, progesterone, and dexamethasone are identified to upregulate TRPV6 expression in the cerebral cortex and hypothalamus of mice suggesting a probable involvement of TRPV6 in calcium absorption in the brain

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