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Effects of parental folate deficiency on the folate content, global DNA methylation, and expressions of FR${\alpha}$, IGF-2 and IGF-1R in the postnatal rat liver

  • Mejos, Karen Kay (Department of Nutritional Science and Food Management, Ewha Womans University) ;
  • Kim, Hye Won (Department of Nutritional Science and Food Management, Ewha Womans University) ;
  • Lim, Eun Mi (Department of Nutritional Science and Food Management, Ewha Womans University) ;
  • Chang, Namsoo (Department of Nutritional Science and Food Management, Ewha Womans University)
  • Received : 2013.02.26
  • Accepted : 2013.05.02
  • Published : 2013.08.01

Abstract

We examined the effect of parental folate deficiency on the folate content, global DNA methylation, folate receptor-alpha (FR${\alpha}$), insulin-like-growth factor-2 (IGF-2) and -1 receptor (IGF-1R) in the liver and plasma homocysteine in the postnatal rat. Male and female rats were randomly fed a folic acid-deficient (paternal folate-deficient, PD and maternal folate-deficient, MD), or folic acid-supplemented diet (paternal folate-supplemented, PS and maternal-folate-supplemented, MS) for four weeks. They were mated and grouped accordingly: $PS{\times}MS$, $PS{\times}MD$, $PD{\times}MS$, and $PD{\times}MD$. Pups were killed on day 21 of lactation. The hepatic folate content was markedly reduced in the $PD{\times}MD$ and $PS{\times}MD$ and $PD{\times}MS$ as compared with the $PS{\times}MS$ group. The hepatic global DNA methylation was decreased in the $PD{\times}MS$ and $PS{\times}MD$ groups as much as in the $PD{\times}MD$ group, and all the three groups were significantly lower as compared to the $PS{\times}MS$ group. There were no significant differences in the hepatic FR${\alpha}$, IGF-2 and IGF-1R expressions among the groups. Positive correlations were found between the hepatic folate content and global DNA methylation and protein expressions of FR${\alpha}$, IGF-2 and IGF-1R, whereas an inverse correlation was found between hepatic folate content and plasma homocysteine level in the 3-week-old rat pup. The results of this study show that both paternal and maternal folate deficiency at mating can influence the folate content and global DNA methylation in the postnatal rat liver.

Keywords

References

  1. Tamura T, Picciano MF. Folate and human reproduction. Am J Clin Nutr 2006;83:993-1016.
  2. Pufulete M, Al-Ghnaniem R, Khushal A, Appleby P, Harris N, Gout S, Emery PW, Sanders TA. Effect of folic acid supplementation on genomic DNA methylation in patients with colorectal adenoma. Gut 2005;54:648-53. https://doi.org/10.1136/gut.2004.054718
  3. Cetin I, Berti C, Calabrese S. Role of micronutrients in the periconceptional period. Hum Reprod Update 2010;16:80-95. https://doi.org/10.1093/humupd/dmp025
  4. Farin CE, Alexander JE, Farin PW. Expression of messenger RNAs for insulin-like growth factors and their receptors in bovine fetuses at early gestation from embryos produced in vivo or in vitro. Theriogenology 2010;74:1288-95. https://doi.org/10.1016/j.theriogenology.2010.05.035
  5. Liu JP, Baker J, Perkins AS, Robertson EJ, Efstratiadis A. Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r). Cell 1993;75: 59-72.
  6. Pedone PV, Cosma MP, Ungaro P, Colantuoni V, Bruni CB, Zarrilli R, Riccio A. Parental imprinting of rat insulin-like growth factor II gene promoters is coordinately regulated. J Biol Chem 1994;269:23970-5.
  7. Overall M, Bakker M, Spencer J, Parker N, Smith P, Dziadek M. Genomic imprinting in the rat: linkage of Igf2 and H19 genes and opposite parental allele-specific expression during embryogenesis. Genomics 1997;45:416-20. https://doi.org/10.1006/geno.1997.4933
  8. Randhawa R, Cohen P. The role of the insulin-like growth factor system in prenatal growth. Mol Genet Metab 2005;86:84-90. https://doi.org/10.1016/j.ymgme.2005.07.028
  9. Wolf E, Hoeflich A, Lahm H. What is the function of IGF-II in postnatal life? Answers from transgenic mouse models. Growth Horm IGF Res 1998;8:185-93. https://doi.org/10.1016/S1096-6374(98)80110-X
  10. Qiu Q, Jiang JY, Bell M, Tsang BK, Gruslin A. Activation of endoproteolytic processing of insulin-like growth factor-II in fetal, early postnatal, and pregnant rats and persistence of circulating levels in postnatal life. Endocrinology 2007;148:4803-11. https://doi.org/10.1210/en.2007-0535
  11. Marks AG, Carroll JM, Purnell JQ, Roberts CT Jr. Plasma distribution and signaling activities of IGF-II precursors. Endocrinology 2011;152:922-30. https://doi.org/10.1210/en.2010-0784
  12. Morison IM, Eccles MR, Reeve AE. Imprinting of insulin-like growth factor 2 is modulated during hematopoiesis. Blood 2000; 96:3023-8.
  13. Wani NA, Nada R, Khanduja KL, Kaur J. Decreased activity of folate transporters in lipid rafts resulted in reduced hepatic folate uptake in chronic alcoholism in rats. Genes Nutr 2013;8:209-19. https://doi.org/10.1007/s12263-012-0318-2
  14. Mato JM, Martinez-Chantar ML, Lu SC. Methionine metabolism and liver disease. Annu Rev Nutr 2008;28:273-93. https://doi.org/10.1146/annurev.nutr.28.061807.155438
  15. Zhao R, Diop-Bove N, Visentin M, Goldman ID. Mechanisms of membrane transport of folates into cells and across epithelia. Annu Rev Nutr 2011;31:177-201. https://doi.org/10.1146/annurev-nutr-072610-145133
  16. Lillycrop KA, Phillips ES, Jackson AA, Hanson MA, Burdge GC. Dietary protein restriction of pregnant rats induces and folic acid supplementation prevents epigenetic modification of hepatic gene expression in the offspring. J Nutr 2005;135:1382-6.
  17. Howell CY, Bestor TH, Ding F, Latham KE, Mertineit C, Trasler JM, Chaillet JR. Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene. Cell 2001;104:829-38. https://doi.org/10.1016/S0092-8674(01)00280-X
  18. Haggarty P, Hoad G, Campbell DM, Horgan GW, Piyathilake C, McNeill G. Folate in pregnancy and imprinted gene and repeat element methylation in the offspring. Am J Clin Nutr 2013;97: 94-9. https://doi.org/10.3945/ajcn.112.042572
  19. Bourque DK, Avila L, Penaherrera M, von Dadelszen P, Robinson WP. Decreased placental methylation at the H19/IGF2 imprinting control region is associated with normotensive intrauterine growth restriction but not preeclampsia. Placenta 2010;31:197-202. https://doi.org/10.1016/j.placenta.2009.12.003
  20. Braunschweig MH, Owczarek-Lipska M, Stahlberger-Saitbekova N. Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2. BMC Genet 2011;12:47.
  21. Gong L, Pan YX, Chen H. Gestational low protein diet in the rat mediates Igf2 gene expression in male offspring via altered hepatic DNA methylation. Epigenetics 2010;5:619-26. https://doi.org/10.4161/epi.5.7.12882
  22. Steegers-Theunissen RP, Obermann-Borst SA, Kremer D, Lindemans J, Siebel C, Steegers EA, Slagboom PE, Heijmans BT. Periconceptional maternal folic acid use of 400 microg per day is related to increased methylation of the IGF2 gene in the very young child. PLoS One 2009;4:e7845. https://doi.org/10.1371/journal.pone.0007845
  23. Hoyo C, Murtha AP, Schildkraut JM, Jirtle RL, Demark- Wahnefried W, Forman MR, Iversen ES, Kurtzberg J, Overcash F, Huang Z, Murphy SK. Methylation variation at IGF2 differentially methylated regions and maternal folic acid use before and during pregnancy. Epigenetics 2011;6:928-36. https://doi.org/10.4161/epi.6.7.16263
  24. Hansen M, Kurinczuk JJ, Bower C, Webb S. The risk of major birth defects after intracytoplasmic sperm injection and in vitro fertilization. N Engl J Med 2002;346:725-30. https://doi.org/10.1056/NEJMoa010035
  25. Carrell DT, Hammoud SS. The human sperm epigenome and its potential role in embryonic development. Mol Hum Reprod 2010;16:37-47. https://doi.org/10.1093/molehr/gap090
  26. Virro MR, Larson-Cook KL, Evenson DP. Sperm chromatin structure assay (SCSA) parameters are related to fertilization, blastocyst development, and ongoing pregnancy in in vitro fertilization and intracytoplasmic sperm injection cycles. Fertil Steril 2004;81:1289-95. https://doi.org/10.1016/j.fertnstert.2003.09.063
  27. Jenkins TG, Carrell DT. The sperm epigenome and potential implications for the developing embryo. Reproduction 2012;143: 727-34. https://doi.org/10.1530/REP-11-0450
  28. Kim HW, Choi YJ, Kim KN, Tamura T, Chang N. Effect of paternal folate deficiency on placental folate content and folate receptor $\alpha$ expression in rats. Nutr Res Pract 2011;5:112-6. https://doi.org/10.4162/nrp.2011.5.2.112
  29. Kim HW, Kim KN, Choi YJ, Chang N. Effects of paternal folate deficiency on the expression of insulin-like growth factor-2 and global DNA methylation in the fetal brain. Mol Nutr Food Res 2013;57:671-6. https://doi.org/10.1002/mnfr.201200558
  30. Baker H, Frank O, Deangelis B, Feingold S, Kaminetzky HA. Role of placenta in maternal-fetal vitamin transfer in humans. Am J Obstet Gynecol 1981;141:792-6. https://doi.org/10.1016/0002-9378(81)90706-7
  31. Solanky N, Requena Jimenez A, D'Souza SW, Sibley CP, Glazier JD. Expression of folate transporters in human placenta and implications for homocysteine metabolism. Placenta 2010;31: 134-43. https://doi.org/10.1016/j.placenta.2009.11.017
  32. Ball GF. Vitamins in Foods: Analysis, Bioavailability, and Stability. Boca Raton (FL): CRC/Taylor & Francis; 2006. p.231-74.
  33. Molloy AM, Mills JL, McPartlin J, Kirke PN, Scott JM, Daly S. Maternal and fetal plasma homocysteine concentrations at birth: the influence of folate, vitamin B12, and the 5,10- methylenetetrahydrofolate reductase 677C-->T variant. Am J Obstet Gynecol 2002;186:499-503. https://doi.org/10.1067/mob.2002.121105
  34. Waterland RA, Michels KB. Epigenetic epidemiology of the developmental origins hypothesis. Annu Rev Nutr 2007;27: 363-88. https://doi.org/10.1146/annurev.nutr.27.061406.093705

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