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Hypoxia inducible factors regulate the transcription of the sprouty2 gene and expression of the sprouty2 protein.
PLoS One. 2017; 12(2):e0171616.Plos

Abstract

Receptor Tyrosine Kinase (RTK) signaling plays a major role in tumorigenesis and normal development. Sprouty2 (Spry2) attenuates RTK signaling and inhibits processes such as angiogenesis, cell proliferation, migration and survival, which are all upregulated in tumors. Indeed in cancers of the liver, lung, prostate and breast, Spry2 protein levels are markedly decreased correlating with poor patient prognosis and shorter survival. Thus, it is important to understand how expression of Spry2 is regulated. While prior studies have focused on the post-translation regulation of Spry2, very few studies have focused on the transcriptional regulation of SPRY2 gene. Here, we demonstrate that in the human hepatoma cell line, Hep3B, the transcription of SPRY2 is inhibited by the transcription regulating hypoxia inducible factors (HIFs). HIFs are composed of an oxygen regulated alpha subunit (HIF1α or HIF2α) and a beta subunit (HIF1β). Intriguingly, silencing of HIF1α and HIF2α elevates SPRY2 mRNA and protein levels suggesting HIFs reduce the transcription of the SPRY2 promoter. In silico analysis identified ten hypoxia response elements (HREs) in the proximal promoter and first intron of SPRY2. Using chromatin immunoprecipitation (ChIP), we show that HIF1α/2α bind near the putative HREs in the proximal promoter and intron of SPRY2. Our studies demonstrated that not only is the SPRY2 promoter methylated, but silencing HIF1α/2α reduced the methylation. ChIP assays also showed DNA methyltransferase1 (DNMT1) binding to the proximal promoter and first intron of SPRY2 and silencing HIF1α/2α decreased this association. Additionally, silencing of DNMT1 mimicked the HIF1α/2α silencing-mediated increase in SPRY2 mRNA and protein. While simultaneous silencing of HIF1α/2α and DNMT1 increased SPRY2 mRNA a little more, the increase was not additive suggesting a common mechanism by which DNMT1 and HIF1α/2α regulate SPRY2 transcription. Together these data suggest that the transcription of SPRY2 is inhibited by HIFs, in part, via DNMT1- mediated methylation.

Authors+Show Affiliations

Department of Surgery, Loyola University Chicago, Chicago, Illinois, United States of America.Department of Pharmaceutical Sciences, Albany College of Pharmacy and Health Sciences, Albany, New York, United States of America.Department of Pharmaceutical Sciences, Albany College of Pharmacy and Health Sciences, Albany, New York, United States of America.Department of Pharmaceutical Sciences, Albany College of Pharmacy and Health Sciences, Albany, New York, United States of America.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

28196140

Citation

Gao, Xianlong, et al. "Hypoxia Inducible Factors Regulate the Transcription of the Sprouty2 Gene and Expression of the Sprouty2 Protein." PloS One, vol. 12, no. 2, 2017, pp. e0171616.
Gao X, Hicks KC, Neumann P, et al. Hypoxia inducible factors regulate the transcription of the sprouty2 gene and expression of the sprouty2 protein. PLoS ONE. 2017;12(2):e0171616.
Gao, X., Hicks, K. C., Neumann, P., & Patel, T. B. (2017). Hypoxia inducible factors regulate the transcription of the sprouty2 gene and expression of the sprouty2 protein. PloS One, 12(2), e0171616. https://doi.org/10.1371/journal.pone.0171616
Gao X, et al. Hypoxia Inducible Factors Regulate the Transcription of the Sprouty2 Gene and Expression of the Sprouty2 Protein. PLoS ONE. 2017;12(2):e0171616. PubMed PMID: 28196140.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Hypoxia inducible factors regulate the transcription of the sprouty2 gene and expression of the sprouty2 protein. AU - Gao,Xianlong, AU - Hicks,Kristin C, AU - Neumann,Paul, AU - Patel,Tarun B, Y1 - 2017/02/14/ PY - 2016/11/04/received PY - 2017/01/23/accepted PY - 2017/2/15/entrez PY - 2017/2/15/pubmed PY - 2017/8/25/medline SP - e0171616 EP - e0171616 JF - PloS one JO - PLoS ONE VL - 12 IS - 2 N2 - Receptor Tyrosine Kinase (RTK) signaling plays a major role in tumorigenesis and normal development. Sprouty2 (Spry2) attenuates RTK signaling and inhibits processes such as angiogenesis, cell proliferation, migration and survival, which are all upregulated in tumors. Indeed in cancers of the liver, lung, prostate and breast, Spry2 protein levels are markedly decreased correlating with poor patient prognosis and shorter survival. Thus, it is important to understand how expression of Spry2 is regulated. While prior studies have focused on the post-translation regulation of Spry2, very few studies have focused on the transcriptional regulation of SPRY2 gene. Here, we demonstrate that in the human hepatoma cell line, Hep3B, the transcription of SPRY2 is inhibited by the transcription regulating hypoxia inducible factors (HIFs). HIFs are composed of an oxygen regulated alpha subunit (HIF1α or HIF2α) and a beta subunit (HIF1β). Intriguingly, silencing of HIF1α and HIF2α elevates SPRY2 mRNA and protein levels suggesting HIFs reduce the transcription of the SPRY2 promoter. In silico analysis identified ten hypoxia response elements (HREs) in the proximal promoter and first intron of SPRY2. Using chromatin immunoprecipitation (ChIP), we show that HIF1α/2α bind near the putative HREs in the proximal promoter and intron of SPRY2. Our studies demonstrated that not only is the SPRY2 promoter methylated, but silencing HIF1α/2α reduced the methylation. ChIP assays also showed DNA methyltransferase1 (DNMT1) binding to the proximal promoter and first intron of SPRY2 and silencing HIF1α/2α decreased this association. Additionally, silencing of DNMT1 mimicked the HIF1α/2α silencing-mediated increase in SPRY2 mRNA and protein. While simultaneous silencing of HIF1α/2α and DNMT1 increased SPRY2 mRNA a little more, the increase was not additive suggesting a common mechanism by which DNMT1 and HIF1α/2α regulate SPRY2 transcription. Together these data suggest that the transcription of SPRY2 is inhibited by HIFs, in part, via DNMT1- mediated methylation. SN - 1932-6203 UR - https://www.unboundmedicine.com/medline/citation/28196140/Hypoxia_inducible_factors_regulate_the_transcription_of_the_sprouty2_gene_and_expression_of_the_sprouty2_protein_ L2 - http://dx.plos.org/10.1371/journal.pone.0171616 DB - PRIME DP - Unbound Medicine ER -