Literature DB >> 26314252

The expression of RNA helicase DDX5 is transcriptionally upregulated by calcitriol through a vitamin D response element in the proximal promoter in SiHa cervical cells.

Ramiro José González-Duarte1,2, Verna Cázares-Ordoñez1,2, Lorenza Díaz1, Víctor Ortíz3, Fernando Larrea1, Euclides Avila4.   

Abstract

The DEAD box RNA helicase DDX5 is a multifunctional protein involved in the regulatory events of gene expression. Herein, we presented evidence indicating that DDX5 is transcriptionally upregulated by calcitriol, the hormonal form of vitamin D3. In silico analysis revealed the presence of two putative vitamin D response elements (VDREs) in the DDX5 promoter region. Using luciferase reporter assays, we demonstrated that the DDX5 promoter containing these putative VDREs significantly increased the luciferase activity in vitamin D receptor (VDR)-positive SiHa cells upon calcitriol treatment. Electrophoretic mobility shift assays showed the ability of VDR and retinoid X receptor to interact only with the most proximal VDRE, while chromatin immunoprecipitation analysis confirmed the occupancy of this VDRE by the VDR. Finally, we demonstrated that calcitriol significantly increased both DDX5 mRNA and protein in SiHa cells. In summary, this study shows that DDX5 gene is transcriptionally upregulated by calcitriol through a VDRE located in its proximal promoter. Given the importance of DDX5 as a master regulator of differentiation programs, our study suggests that the pro-differentiating properties of calcitriol may be related with the induction of DDX5.

Entities:  

Keywords:  Cervical cancer; Nuclear receptor; RNA helicase; VDR; Vitamin D

Mesh:

Substances:

Year:  2015        PMID: 26314252     DOI: 10.1007/s11010-015-2538-4

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  35 in total

1.  p68 DEAD box RNA helicase expression in keratinocytes. Regulation, nucleolar localization, and functional connection to proliferation and vascular endothelial growth factor gene expression.

Authors:  Kornelija Kahlina; Itamar Goren; Josef Pfeilschifter; Stefan Frank
Journal:  J Biol Chem       Date:  2004-08-10       Impact factor: 5.157

2.  Sumoylation of p68 and p72 RNA helicases affects protein stability and transactivation potential.

Authors:  Steven M Mooney; Joseph P Grande; Jeffrey L Salisbury; Ralf Janknecht
Journal:  Biochemistry       Date:  2010-01-12       Impact factor: 3.162

3.  Calcitriol increases Dicer expression and modifies the microRNAs signature in SiHa cervical cancer cells.

Authors:  Ramiro José González-Duarte; Verna Cázares-Ordoñez; Sandra Romero-Córdoba; Lorenza Díaz; Víctor Ortíz; Julio Augusto Freyre-González; Alfredo Hidalgo-Miranda; Fernando Larrea; Euclides Avila
Journal:  Biochem Cell Biol       Date:  2015-05-20       Impact factor: 3.626

4.  Injury enhances TLR2 function and antimicrobial peptide expression through a vitamin D-dependent mechanism.

Authors:  Jürgen Schauber; Robert A Dorschner; Alvin B Coda; Amanda S Büchau; Philip T Liu; David Kiken; Yolanda R Helfrich; Sewon Kang; Hashem Z Elalieh; Andreas Steinmeyer; Ulrich Zügel; Daniel D Bikle; Robert L Modlin; Richard L Gallo
Journal:  J Clin Invest       Date:  2007-02-08       Impact factor: 14.808

Review 5.  The sum of many small changes: microRNAs are specifically and potentially globally altered by vitamin D3 metabolites.

Authors:  Angeline A Giangreco; Larisa Nonn
Journal:  J Steroid Biochem Mol Biol       Date:  2013-01-16       Impact factor: 4.292

6.  p68 (Ddx5) interacts with Runx2 and regulates osteoblast differentiation.

Authors:  Eric D Jensen; Lingling Niu; Giuseppina Caretti; Samantha M Nicol; Nadiya Teplyuk; Gary S Stein; Vittorio Sartorelli; Andre J van Wijnen; Frances V Fuller-Pace; Jennifer J Westendorf
Journal:  J Cell Biochem       Date:  2008-04-01       Impact factor: 4.429

7.  Functional interaction between Smad, CREB binding protein, and p68 RNA helicase.

Authors:  Dennis R Warner; Vasker Bhattacherjee; Xiaolong Yin; Saurabh Singh; Partha Mukhopadhyay; M Michele Pisano; Robert M Greene
Journal:  Biochem Biophys Res Commun       Date:  2004-11-05       Impact factor: 3.575

Review 8.  Coupling transcription to RNA processing via the p68 DEAD box RNA helicase androgen receptor co-activator in prostate cancer.

Authors:  Emma L Clark; Frances V Fuller-Pace; David J Elliott; Craig N Robson
Journal:  Biochem Soc Trans       Date:  2008-06       Impact factor: 5.407

9.  SUMO modification of the DEAD box protein p68 modulates its transcriptional activity and promotes its interaction with HDAC1.

Authors:  A-M F Jacobs; S M Nicol; R G Hislop; E G Jaffray; R T Hay; F V Fuller-Pace
Journal:  Oncogene       Date:  2007-03-19       Impact factor: 9.867

10.  The RNA helicase Ddx5/p68 binds to hUpf3 and enhances NMD of Ddx17/p72 and Smg5 mRNA.

Authors:  Verena Geißler; Simone Altmeyer; Benjamin Stein; Heike Uhlmann-Schiffler; Hans Stahl
Journal:  Nucleic Acids Res       Date:  2013-06-20       Impact factor: 16.971

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  2 in total

1.  Transcriptome profiling of human oocytes experiencing recurrent total fertilization failure.

Authors:  Lun Suo; Yu Xiao Zhou; Li Ling Jia; Hai Bo Wu; Jin Zheng; Qi Feng Lyu; Li Hua Sun; Han Sun; Yan Ping Kuang
Journal:  Sci Rep       Date:  2018-12-17       Impact factor: 4.379

Review 2.  Vitamin D and VDR in Gynecological Cancers-A Systematic Review.

Authors:  Eileen Deuster; Udo Jeschke; Yao Ye; Sven Mahner; Bastian Czogalla
Journal:  Int J Mol Sci       Date:  2017-11-04       Impact factor: 5.923

  2 in total

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