suck pdf from google scholar
PDF vom PMID16002434  :  Publisher
PDF vom PMID16002434
suck pdf from library genesis
English Wikipedia

Nephropedia Template TP (

Twit Text


  • DeepDyve
  • Pubget Overpricing


  • lüll
  • Large-scale in silico and microarray-based identification of direct 1,25-dihydroxyvitamin D3 target genes
  • Wang TT; Tavera-Mendoza LE; Laperriere D; Libby E; MacLeod NB; Nagai Y; Bourdeau V; Konstorum A; Lallemant B; Zhang R; Mader S; White JH
  • Mol Endocrinol 2005[Nov]; 19 (11): 2685-95
  • 1alpha,25-Dihydroxyvitamin D3 [1,25(OH)2D3] regulates calcium homeostasis and controls cellular differentiation and proliferation. The vitamin D receptor (VDR) is a ligand-regulated transcription factor that recognizes cognate vitamin D response elements (VDREs) formed by direct or everted repeats of PuG(G/T)TCA motifs separated by 3 or 6 bp (DR3 or ER6). Here, we have identified direct 1,25(OH)2D3 target genes by combining 35,000+ gene microarrays and genome-wide screens for consensus DR3 and ER6 elements, and DR3 elements containing single nucleotide substitutions. We find that the effect of a nucleotide substitution on VDR binding in vitro does not predict VDRE function in vivo, because substitutions that disrupted binding in vitro were found in several functional elements. Hu133A microarray analyses, performed with RNA from human SCC25 cells treated with 1,25(OH)2D3 and protein synthesis inhibitor cycloheximide, identified more than 900 regulated genes. VDREs lying within -10 to +5 kb of 5'-ends were assigned to 65% of these genes, and VDR binding was confirmed to several elements in vivo. A screen of the mouse genome identified more than 3000 conserved VDREs, and 158 human genes containing conserved elements were 1,25(OH2)D3-regulated on Hu133A microarrays. These experiments also revealed 16 VDREs in 11 of 12 genes induced more than 10-fold in our previous microarray study, five elements in the human gene encoding the epithelial calcium channel TRPV6, as well as novel 1,25(OH2)D3 target genes implicated in regulation of cell cycle progression. The combined approaches used here thus provide numerous insights into the direct target genes underlying the broad physiological actions of 1,25(OH)2D3.
  • |*Gene Expression Regulation[MESH]
  • |Animals[MESH]
  • |Base Sequence[MESH]
  • |Calcitriol/*physiology[MESH]
  • |Cell Line[MESH]
  • |Conserved Sequence[MESH]
  • |Gene Expression Profiling[MESH]
  • |Humans[MESH]
  • |Mice[MESH]
  • |Molecular Sequence Data[MESH]
  • |Mutation[MESH]
  • |Oligonucleotide Array Sequence Analysis[MESH]
  • |Receptors, Calcitriol/*metabolism[MESH]
  • |Tandem Repeat Sequences[MESH]
  • |Vitamin D Response Element/*genetics/physiology[MESH]





  • *{{pmid16002434}}
    *<b>[http://www.kidney.de/mlpefetch.php?search=16002434 Large-scale in silico and microarray-based identification of direct 1,25-dihydroxyvitamin D3 target genes ]</b> Mol Endocrinol 2005; 19(11) ; 2685-95 Wang TT; Tavera-Mendoza LE; Laperriere D; Libby E; MacLeod NB; Nagai Y; Bourdeau V; Konstorum A; Lallemant B; Zhang R; Mader S; White JH

        *16002434*

    Nephropedia PMID record

    Deutsche Wikipedia - im Artikel

    Hier den unten stehenden Textblock hineinkopieren

    Mol Endocrinol

    2685 11.19 2005