ESR1-Mediated Regulation of Slc2a4 Gene Expression by Estrogen: Demonstration of a Potential Estrogen Responsive Element (ERE) in the Slc2a4 Gene Promoter

Authors

  • Caroline Pancera Laurindo Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, SP, Brazil
  • Karen Cristina Rego Gregorio Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, SP, Brazil
  • Helayne Soares de Freitas Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, SP, Brazil
  • Camila Nogueira Alves Bezerra Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, SP, Brazil
  • Maristela Mitiko Okamoto Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, SP, Brazil
  • Patricia Monteiro Seraphim Department of Physiotherapy, School of Science and Technology, Sao Paulo State University (UNESP), Presidente Prudente, 19060-900, SP, Brazil
  • William Tadeu Festuccia Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, SP, Brazil
  • Ubiratan Fabres Machado Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-000, SP, Brazil

DOI:

https://doi.org/10.14738/bjhr.1302.20178

Keywords:

diabetes mellitus, insulin resistance, GLUT4, 17β-estradiol, PPT, estrogen receptor

Abstract

This study investigated the transcriptional activity (gene reporter assay) of some putative estrogen responsive elements (EREs) in the Slc2a4 gene promoter region, which could contribute to understanding the estrogen receptor 1 (ESR1) mediated enhancer role of estradiol (E2). In 3T3L1 adipocytes, E2 and ESR1-selective agonist (PPT) increased (by 35%, p<0.01) the expression of Slc2a4 mRNA; ESR1-selective antagonist (MPP) abrogated the E2 effect. In transiently transfected HEK293-FT cells, the basal Slc2a4-Luciferase activity of 5’-500, 5’-250 and 5’-149 bp segments of the promoter revealed that the loss of the -500/-250 bp segment reduces the unstimulated Slc2a4-Luc activity (60%, p<0.001), a response attributed to the loss of seven known binding-sites of enhancer transcription factors. Besides, E2/PPT increased (~150%, p<0.001) the relative Slc2a4-Luc activity of all constructs, revealing that the ESR1-mediated E2-induced transcriptional activity is preserved in all constructs, and that the putative ERE half-sites, encompassed in -250/-149 bp segment, do not display transcriptional activity. Finally, 5’-500 bp and 5’-149 bp constructs, containing four mutated nucleotides in the putative complete Slc2a4 ERE, lost their responsiveness to E2. In conclusion, this study reveals an imperfect complete Slc2a4 ERE site (-59/-46 bp), which is involved in the ESR1-mediated E2-induced enhancing of the Slc2a4 gene expression.

References

Gessler, C.J.; Halsted, J.A.; Stetson, R.P. Effect of estrogenic substance on the blood sugar of female diabetics after the menopause. J. Clin. Investig. 1939, 18, 715–722.

Rasio, E.; Antaki, A.; Campenhout, J. Diabetes Mellitus in Gonadal Dysgenesis: Studies of Insulin and Growth Hormone Secretion. Eur. J. Clin. Investig. 1976, 6, 59–66.

Polychronakos, C.; Letarte, J.; Collu, R.; Ducharme, J. Carbohydrate intolerance in children and adolescents with Turner syndrome. J. Pediatr. 1980, 96, 1009–1014.

Carr, M.C. The emergence of the metabolic syndrome with menopause. J. Clin. Endocrinol. Metab. 2003, 88, 2404–2411.

Dunaif, A.; Segal, K.R.; Futterweit, W.; Dobrjansky, A. Profound peripheral insulin resistance, independent of obesity, in polycystic ovary syndrome. Diabetes 1989, 38, 1165–1174.

Livingstone, C.; Collison, M. Sex steroids and insulin resistance. Clin. Sci. 2002, 102, 151–166.

Lopez, L.M.; Grimes, D.A.; Schulz, K.F. Steroidal contraceptives: Effect on carbohydrate metabolism in women without diabetes mellitus. Cochrane Database Syst. Rev. 2014, 2019,

Smith, E.P.; Boyd, J.; Frank, G.R.; Takahashi, H.; Cohen, R.M.; Specker, B.;Williams, T.C.; Lubahn, D.B.; Korach, K.S. Estrogen Resistance Caused by a Mutation in the Estrogen-Receptor Gene in a Man. N. Engl. J. Med. 1994, 331, 1056–1061.

Faustini-Fustini, M.; Rochira, V.; Carani, C. Oestrogen deficiency in men: Where are we today? Eur. J. Endocrinol. 1999, 140, 111–129.

Elbers, J.M.H.; Giltay, E.J.; Teerlink, T.; Scheffer, P.G.; Asscheman, H.; Seidell, J.C.; Gooren, L.J.G. Effects of sex steroids on components of the insulin resistance syndrome in transsexual subjects. Clin. Endocrinol. 2003, 58, 562–571.

Belgorosky, A.; Guercio, G.; Pepe, C.; Saraco, N.; Rivarola, M. Genetic and Clinical Spectrum of Aromatase Deficiency in Infancy, Childhood and Adolescence. Horm. Res. Paediatr. 2009, 72, 321–330.

Mueckler, M.; Thorens, B. The SLC2 (GLUT) family of membrane transporters. Mol. Asp. Med.

Klip, A.; McGraw, T.E.; James, D.E. Thirty sweet years of GLUT4. J. Biol. Chem. 2019, 294, 11369–11381.

Machado, U.F.; Shimizu, I.; Saito, M. Reduced content and preserved translocation of glucose transporter (GLUT 4) in white adipose tissue of obese mice. Physiol. Behav. 1994, 55, 621–

Nilsson, S.; Mäkelä, S.; Treuter, E.; Tujague, M.; Thomsen, J.; Andersson, G.; Enmark, E.; Pettersson, K.;Warner, M.; Gustafsson, J.-Å. Mechanisms of Estrogen Action. Physiol. Rev.

Heldring, N.; Pike, A.; Andersson, S.; Matthews, J.; Cheng, G.; Hartman, J.; Tujague, M.; Ström, A.; Treuter, E.; Warner, M.; Gustafsson J.-A. Estrogen Receptors: How Do They Signal and What Are Their Targets. Physiol. Rev. 2007, 87, 905–931. Scholar Publishing

Eriksson, M.A.L.; Nilsson, L. Structural and dynamic differences of the estrogen receptor DNA-binding domain, binding as a dimer and as a monomer to DNA: Molecular dynamics simulation studies. Eur. Biophys. J. 1999, 28, 102–111.

Safe, S. Transcriptional activation of genes by 17β-estradiol through estrogen receptor-Sp1 interactions. Vitam. Horm. 2001, 62, 231–252.

Hewitt, S.C.; Li, Y.; Li, L.; Korach, K.S. Estrogen-mediated Regulation of Igf1 Transcription and Uterine Growth Involves Direct Binding of Estrogen Receptor α to Estrogen-responsive Elements. J. Biol. Chem. 2009, 285, 2676–2685.

Liu, D.; Deschamps, A.; Korach, K.S.; Murphy, E. Estrogen-Enhanced Gene Expression of Lipoprotein Lipase in Heart Is Antagonized by Progesterone. Endocrinology, 2007, 149, 711–

Safe, S.; Kim, K. Non-classical genomic estrogen receptor (ER)/specificity protein and ER/activating protein-1 signaling pathways. J. Mol. Endocrinol. 2008, 41, 263–275.

Barros, R.P.A.; Machado, U.F.; Warner, M.N.; Gustafsson, J.-Å. Muscle GLUT4 regulation by estrogen receptors ERβ and ERα. Proc. Natl. Acad. Sci. USA. 2006, 103, 1605–1608.

Barros, R.P.; Machado, U.F.; Gustafsson, J.-Å. Estrogen receptors: New players in diabetes mellitus. Trends Mol. Med. 2006, 12, 425–431.

Barros, R.P.A.; Gabbi, C.; Morani, A.; Warner, M.; Gustafsson, J.-Å. Participation of ERα and ERβ in glucose homeostasis in skeletal muscle and white adipose tissue. AJP Endocrinol. Metab. 2009, 297, E124–E133.

Barros, R.P.; Gustafsson, J.-Å. Estrogen Receptors and the Metabolic Network. Cell. Metab.

Giannella, M.L.C.C.; Machado, U.F. SLC2A4gene: A promising target for pharmacogenomics of insulin resistance. Pharmacogenomics 2013, 14, 847–850.

Gregorio, K.C.R.; Laurindo, C.P.; Machado, U.F. Estrogen and Glycemic Homeostasis: The Fundamental Role of Nuclear Estrogen Receptors ESR1/ESR2 in Glucose Transporter GLUT4 Regulation. Cells., 2021; 10, 99.

Im, S-S.; Kwon, S.-K.; Kim, T.-H.; Kim, H.; Ahn, Y.-H. Regulation of glucose transporter type 4 isoform gene expression in muscle and adipocytes. IUBMB Life 2007, 59, 134–145.

Karnieli, E.; Armoni, M. Transcriptional regulation of the insulin-responsive glucose transporter GLUT4 gene: From physiology to pathology. Am. J. Physiol. Metab. 2008, 295, E38–E45.

Kaestner, K.H.; Christy, R.J.; Lane, M.D. Mouse insulin-responsive glucose transporter gene: characterization of the gene and trans-activation by the CCAAT/enhancer binding protein. Proc. Natl. Acad. Sci. USA. 1990, 87, 251-5.

Liu, M.L.; Olson, A.L.; Edgington, N.P.; Moye-Rowley, W.S.; Pessin, J.E. Myocyte enhancer factor 2 (MEF2) binding site is essential for C2C12 myotube-specific expression of the rat GLUT4/muscle-adipose facilitative glucose transporter gene. J. Biol. Chem. 1994, 269, 28514-

Torrance, C.J.; Usala, S.J.; Pessin, J.E.; Dohm, G.L. Characterization of a low affinity thyroid hormone receptor binding site within the rat GLUT4 gene promoter. Endocrinology 1997, 138, 1215-23.

Santalucía, T.; Moreno, H.; Palacín, M.; Yacoub, M.H.; Brand, N.J.; Zorzano, A. A novel functional co-operation between MyoD, MEF2 and TRalpha1 is sufficient for the induction of GLUT4 gene transcription. J Mol Biol. 2001, 314, 195-204. Scholar Publishing

Gray, S.; Feinberg, M.W.; Hull, S.; Kuo, C.T.; Watanabe, M.; Sen-Banerjee, S.; DePina, A; Haspel, R.; Jain, M.K. The Krüppel-like factor KLF15 regulates the insulin-sensitive glucose transporter GLUT4. J. Biol. Chem. 2002, 277, 34322-8.

Dalen, K.T.; Ulven S.M.; Bamberg, K.; Gustafsson, J-A.; Nebb, H.I. Expression of the insulinresponsive glucose transporter GLUT4 in adipocytes is dependent on liver X receptor alpha. J. Biol. Chem. 2003, 28, 48283-48291.

Im, S.-S.; Kwon, S.-K.; Kang, S.-Y.; Kim, T.-H.; Kim, H.-I.; Hur, M.-W.; Kim, K.-S.; Ahn, Y.-H. Regulation of GLUT4 gene expression by SREBP-1c in adipocytes. Biochem. J. 2006, 399, 131-

Furuya, D.T.; Neri, E.A.; Poletto, A.C.; Anhê, G.F.; Freitas, H.S.; Campello, R.S.; Rebouças, N.A.; Machado, U.F. Identification of nuclear factor-kappaB sites in the Slc2a4 gene promoter. Mol. Cell. Endocrinol. 2013, 370, 87–95.

Alves-Wagner, A.B.; Yonamine, C.Y.; Fatima, L.A.; Festuccia, W.; Machado, F.M. Sympathetic regulation of Slc2a4 gene expression: Participation of a putative cAMP responsive element (CRE) site in the Slc2a4 promoter. Cell Physiol Biochem. 2019, 52, 580-594.

Campello, R.S.; Fatima, L.A.; Barreto-Andrade, J.N.; Lucas, T.F.; Mori, R.C.; Porto, C.S.; Machado, U.F. Estradiol-induced regulation of GLUT4 in 3T3-L1 cells: Involvement of ESR1 and AKT activation. J. Mol. Endocrinol. 2017, 59, 257–268.

Fatima, L.A.; Campello, R.S.; Barreto-Andrade, J.N.; Passarelli, M.; Santos, R.S.; Clegg DJ.; Machado, U.F. Estradiol stimulates adipogenesis and Slc2a4/GLUT4 expression via ESR1-mediated activation of CEBPA. Mol. Cell. Endocrinol. 2019, 498, 110447.

Campello, R.S.; Alves-Wagner, A.B.; Lucas, T.F.; Mori, R.C.; Furuya, D.T.; Porto, C.S.; Machado, U.F. Estrogen receptor 1 agonist PPT stimulates Slc2a4 gene expression and improves insulin-induced glucose uptake in adipocytes. Curr. Top. Med. Chem. 2012, 12, 2059–2069.

Pfeilschifter, J.; Köditz, R.; Pfohl, M.; Schatz, H. Changes in proinflammatory cytokine activity after menopause. Endocr. Rev. 2002, 23, 90–119.

Tchernof, A.; Desmeules, A.; Richard, C.; Laberge, P.; Daris, M.; Mailloux, J.; et al., Ovarian hormone status and abdominal visceral adipose tissue metabolism. J. Clin. Endocrinol. Metab.

Meyer, M.R.; Clegg, D.J.; Prossnitz, E.R.; Barton, M. Obesity, insulin resistance and diabetes: Sex differences and role of oestrogen receptors. Acta Physiol. 2010, 203, 259–269.

Stubbins, R.E.; Holcomb, V.B.; Hong, J.; Núñez, N.P. Estrogen modulates abdominal adiposity and protects female mice from obesity and impaired glucose tolerance. Eur. J. Nutr. 2012, 51, 861–870.

Gustafson, B.; Hedjazifar, S.; Gogg, S.; Hammarstedt, A.; Smith, U. Insulin resistance and impaired adipogenesis. Trends Endocrinol. Metabol. 2015, 26, 193–200.

Barreto-Andrade, J.N.; De Fátima, L.A.; Campello, R.S.; Guedes, J.A.C.; De Freitas, H.S.; Machado, M.M.O.U.F. Estrogen Receptor 1(ESR1) Enhances Slc2a4/GLUT4 Expression by a SP1 Cooperative Mechanism. Int. J. Med. Sci. 2018, 15, 1320–1328.

Torre, S.D.; Rando, G.; Meda, C.; Ciana, P.; Ottobrini, L.; Maggi, A. Transcriptional activity of oestrogen receptors in the course of embryo development. J. Endocrinol. 2018, 238, 165-Scholar Publishing

O'Connor, L.; Gilmour, J.; Bonifer, C. The Role of the Ubiquitously Expressed Transcription Factor Sp1 in Tissue-specific Transcriptional Regulation and in Disease. Yale J. Biol. Med. 2016, 89, 513-525.

Armoni, M.; Harel, C.; Karnieli, E. Transcriptional regulation of the GLUT4 gene: From PPAR-and FOXO1 to FFA and inflammation. Trends Endocrinol. Metab. 2007, 18, 100–107.

Chandra, V.; Huang, P.; Hamuro, Y.; Raghuram, S.; Wang, Y.; Burris, T.P.; Rastinejad, F. Structure of the intact PPAR—RXR nuclear receptor complex on DNA. Nature. 2008, 456, 350–

Armoni, M.; Kritz, N.; Harel, C.; Bar-Yoseph, F.; Chen, H.; Quon, M.J.; Karnieli, E. Peroxisome Proliferator-activated Receptor Represses GLUT4 Promoter Activity in Primary Adipocytes, and Rosiglitazone Alleviates This Effect. J. Biol. Chem. 2003, 278, 30614–30623.

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Published

2026-04-01

How to Cite

Laurindo, C. P., Gregorio, K. C. R., de Freitas, H. S., Bezerra, C. N. A., Okamoto, M. M., Seraphim, P. M., … Machado, U. F. (2026). ESR1-Mediated Regulation of Slc2a4 Gene Expression by Estrogen: Demonstration of a Potential Estrogen Responsive Element (ERE) in the Slc2a4 Gene Promoter. British Journal of Healthcare and Medical Research, 13(02), 154–169. https://doi.org/10.14738/bjhr.1302.20178