Mechanism of vitamin D3-induced transcription of phospholipase D1 in HaCat human keratinocytes

Ryosuke Kikuchi; Sayaka Sobue; Masashi Murakami; Hiromi Ito; Ami Kimura; Takashi Iwasaki; Shuji Shibayama; Akira Takagi; Tetsuhito Kojima; Motoshi Suzuki; Yoshiko Banno; Yoshinori Nozawa; Takashi Murate

doi:10.1016/j.febslet.2007.03.073

Mechanism of vitamin D₃-induced transcription of phospholipase D1 in HaCat human keratinocytes

Ryosuke Kikuchi
, Sayaka Sobue
, Masashi Murakami
, Hiromi Ito
, Ami Kimura
, Takashi Iwasaki
, Shuji Shibayama
, Akira Takagi
, Tetsuhito Kojima
, Motoshi Suzuki
, Yoshiko Banno
, Yoshinori Nozawa
, Takashi Murate

Research output: Contribution to journal › Article › peer-review

12 Citations (Scopus)

Abstract

1α,25-Dihydroxyvitamin D₃ (VitD₃) increases protein and gene expression of phospholipase D1 (PLD1), but not PLD2, in HaCaT human keratinocytes. We show that VitD₃ increases PLD1 gene expression through a vitamin D responsive element (VDRE) on the 5′ PLD1 promoter (-260 bp to -246 bp from exon 1). Similar results were obtained by transfecting VitD₃ receptor (VDR) into HEK293 cells, which are originally VitD₃-unresponsive. Electrophoresis mobility shift assays (EMSA) and chromatin immunoprecipitation (CHIP) assays showed that the complex of VitD₃, VDR and retinoid X receptor α (RXRα) binds to the VDRE and increases PLD1 gene expression in HaCaT cells.

Original language	English
Pages (from-to)	1800-1804
Number of pages	5
Journal	FEBS Letters
Volume	581
Issue number	9
DOIs	https://doi.org/10.1016/j.febslet.2007.03.073
Publication status	Published - 01-05-2007
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biophysics
Structural Biology
Biochemistry
Molecular Biology
Genetics
Cell Biology

Access to Document

10.1016/j.febslet.2007.03.073

Cite this

@article{a33db5d4ea474070b77ab0f12805fa73,

title = "Mechanism of vitamin D3-induced transcription of phospholipase D1 in HaCat human keratinocytes",

abstract = "1α,25-Dihydroxyvitamin D3 (VitD3) increases protein and gene expression of phospholipase D1 (PLD1), but not PLD2, in HaCaT human keratinocytes. We show that VitD3 increases PLD1 gene expression through a vitamin D responsive element (VDRE) on the 5′ PLD1 promoter (-260 bp to -246 bp from exon 1). Similar results were obtained by transfecting VitD3 receptor (VDR) into HEK293 cells, which are originally VitD3-unresponsive. Electrophoresis mobility shift assays (EMSA) and chromatin immunoprecipitation (CHIP) assays showed that the complex of VitD3, VDR and retinoid X receptor α (RXRα) binds to the VDRE and increases PLD1 gene expression in HaCaT cells.",

keywords = "1α,25-Dihydroxyvitamin D, PLD1 gene expression, Promoter analysis, RXRα, VDR",

author = "Ryosuke Kikuchi and Sayaka Sobue and Masashi Murakami and Hiromi Ito and Ami Kimura and Takashi Iwasaki and Shuji Shibayama and Akira Takagi and Tetsuhito Kojima and Motoshi Suzuki and Yoshiko Banno and Yoshinori Nozawa and Takashi Murate",

year = "2007",

month = may,

day = "1",

doi = "10.1016/j.febslet.2007.03.073",

language = "English",

volume = "581",

pages = "1800--1804",

journal = "FEBS Letters",

issn = "0014-5793",

publisher = "John Wiley and Sons Inc.",

number = "9",

}

TY - JOUR

T1 - Mechanism of vitamin D3-induced transcription of phospholipase D1 in HaCat human keratinocytes

AU - Kikuchi, Ryosuke

AU - Sobue, Sayaka

AU - Murakami, Masashi

AU - Ito, Hiromi

AU - Kimura, Ami

AU - Iwasaki, Takashi

AU - Shibayama, Shuji

AU - Takagi, Akira

AU - Kojima, Tetsuhito

AU - Suzuki, Motoshi

AU - Banno, Yoshiko

AU - Nozawa, Yoshinori

AU - Murate, Takashi

PY - 2007/5/1

Y1 - 2007/5/1

N2 - 1α,25-Dihydroxyvitamin D3 (VitD3) increases protein and gene expression of phospholipase D1 (PLD1), but not PLD2, in HaCaT human keratinocytes. We show that VitD3 increases PLD1 gene expression through a vitamin D responsive element (VDRE) on the 5′ PLD1 promoter (-260 bp to -246 bp from exon 1). Similar results were obtained by transfecting VitD3 receptor (VDR) into HEK293 cells, which are originally VitD3-unresponsive. Electrophoresis mobility shift assays (EMSA) and chromatin immunoprecipitation (CHIP) assays showed that the complex of VitD3, VDR and retinoid X receptor α (RXRα) binds to the VDRE and increases PLD1 gene expression in HaCaT cells.

AB - 1α,25-Dihydroxyvitamin D3 (VitD3) increases protein and gene expression of phospholipase D1 (PLD1), but not PLD2, in HaCaT human keratinocytes. We show that VitD3 increases PLD1 gene expression through a vitamin D responsive element (VDRE) on the 5′ PLD1 promoter (-260 bp to -246 bp from exon 1). Similar results were obtained by transfecting VitD3 receptor (VDR) into HEK293 cells, which are originally VitD3-unresponsive. Electrophoresis mobility shift assays (EMSA) and chromatin immunoprecipitation (CHIP) assays showed that the complex of VitD3, VDR and retinoid X receptor α (RXRα) binds to the VDRE and increases PLD1 gene expression in HaCaT cells.

KW - 1α,25-Dihydroxyvitamin D

KW - PLD1 gene expression

KW - Promoter analysis

KW - RXRα

KW - VDR

UR - https://www.scopus.com/pages/publications/34247162737

UR - https://www.scopus.com/pages/publications/34247162737#tab=citedBy

U2 - 10.1016/j.febslet.2007.03.073

DO - 10.1016/j.febslet.2007.03.073

M3 - Article

C2 - 17433303

AN - SCOPUS:34247162737

SN - 0014-5793

VL - 581

SP - 1800

EP - 1804

JO - FEBS Letters

JF - FEBS Letters

IS - 9

ER -

Mechanism of vitamin D₃-induced transcription of phospholipase D1 in HaCat human keratinocytes

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this