The effect of folic acid deficiency on Mest/Peg1 in neural tube defects

Refrences

• Detrait ERG, Etchevers TM, Gilbert HC, et al. Human neural tube defects: developmental biology, epidemiology, and genetics. Neurotoxicol Teratol. 2005;27(3):515–524.
   PubMed Web of Science ®Google Scholar
• Salih MAM, WR, Seidahmed MZ. Epidemiology, prenatal management, and prevention of neural tube defects. Saudi Med J. 2014; 5 (Suppl 1):S15–S28.
   Google Scholar
• Strohle A. Folic acid and neural tube defects: dose-response relationship confirmed. Medizinische Monatsschrift Fur Pharmazeuten. 2014;37(11):419–420.
   PubMedGoogle Scholar
• Kaneko-Ishino T, Kuroiwa Y, Miyoshi N, et al. Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nat Genet. 1995;11(1):52–59.
   PubMed Web of Science ®Google Scholar
• Lefebvre L, Viville S, Barton SC, et al. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet. 1998;20(2):163–169.
   PubMed Web of Science ®Google Scholar
• Ineson J, Stayner C, Hazlett J, et al. Somatic reactivation of expression of the silent maternal Mest allele and acquisition of normal reproductive behaviour in a colony of Peg1/Mest mutant mice. J Reprod Dev. 2012;58(4):490–500.
   PubMed Web of Science ®Google Scholar
• Li T, Vu TH, Lee KO, et al. An imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoa. J Biol Chem. 2002;277(16):13518–13527.
   PubMed Web of Science ®Google Scholar
• Nakabayashi K, Bentley L, Hitchins MP, et al. Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32. Human Molec Genet. 2002;11(15):1743–1756.
   PubMed Web of Science ®Google Scholar
• Mesman S, van Hooft JA, Smidt MP. Mest/Peg1 Is Essential for the Development and Maintenance of a SNc Neuronal Subset. Front Mol Neurosci. 2017;9:166.
   PubMed Web of Science ®Google Scholar
• Lefebvre L, Viville S, Barton SC, et al. Genomic structure and parent-of-origin-specific methylation of Peg1. Human Molec Genet. 1997;6(11):1907–1915.
   PubMed Web of Science ®Google Scholar
• Kerjean AD, Vasseur JM, Le Tessier C, et al. Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis. Human Molec Genet. 2000;9(14):2183–2187.
   PubMed Web of Science ®Google Scholar
• Lucifero D, Mertineit C, Clarke HJ, et al. Methylation dynamics of imprinted genes in mouse germ cells. Genomics. 2002;79(4):530–538.
   PubMed Web of Science ®Google Scholar
• Imamura T, Kerjean A, Heams T, et al. Dynamic CpG and non-CpG methylation of the Peg1/Mest gene in the mouse oocyte and preimplantation embryo. J Biol Chem. 2005;280(20):20171–20175.
   PubMed Web of Science ®Google Scholar
• Jung H, Lee SK, Jho EH. Mest/Peg1 inhibits Wnt signalling through regulation of LRP6 glycosylation. Biochem J. 2011;436(2):263–269.
   PubMed Web of Science ®Google Scholar
• Hamblet NSL, Ruiz-Lozano N, Wang P, et al. Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure. Development (Cambridge, England). 2002;129(24):5827–5838.
   PubMed Web of Science ®Google Scholar
• Carter MC, Slowinska X, Minnerath B, et al. Crooked tail (Cd) model of human folate-responsive neural tube defects is mutated in Wnt coreceptor lipoprotein receptor-related protein 6. PNAS. 2005;102(36):12843–12848.
   PubMed Web of Science ®Google Scholar
• Wang L, Wang F, Guan J, et al. Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects. Am J Clin Nutrit. 2010; 91(5):1359–1367.
   PubMed Web of Science ®Google Scholar
• Chang S, Wang L, Guan Y, et al. Long interspersed nucleotide element-1 hypomethylation in folate-deficient mouse embryonic stem cells. J Cell Biochem. 2013;114(7):1549–1558.
   PubMed Web of Science ®Google Scholar
• Kuramochi-Miyagawa S, Watanabe T, Gotoh K, et al. DNA methylation of retrotransposon genes is regulated by Piwi family members MILI and MIWI2 in murine fetal testes. Genes Develop. 2008;22(7):908–917.
   PubMed Web of Science ®Google Scholar
• Imbard A, Benoist JF, Blom HJ. Neural tube defects, folic acid and methylation. IJERPH. 2013;10(9):4352–4389.
   Web of Science ®Google Scholar
• Wang L, Chang S, Guan J, et al. Tissue-specific methylation of long interspersed nucleotide element-1 of homo sapiens (L1Hs) during human embryogenesis and roles in neural tube defects. CMM. 2015;15(5):497–507.
   PubMed Web of Science ®Google Scholar
• Rochtus A, Jansen K, Geet C, et al. Nutri-epigenomic Studies Related to Neural Tube Defects: Does Folate Affect Neural Tube Closure Via Changes in DNA methylation? MRMC. 2015;15(13):1095–1102.
   Web of Science ®Google Scholar
• Wang L, Wang F, Guan J, et al. Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects. Amer J Clin Nutrit. 2010;91(5):1359–1367.
   PubMed Web of Science ®Google Scholar
• Wu J, Lu X, Wang Z, et al. Association between PKA gene polymorphism and NTDs in high risk Chinese population in Shanxi. Int J Clin Exp Pathol. 2013;6(12):2968–2974.
   PubMed Web of Science ®Google Scholar
• Wang Z, Shangguan S, Lu X, et al. Association of SMO polymorphisms and neural tube defects in the Chinese population from Shanxi Province. Int J Clin Exp Med. 2013;6(10):960–966.
   PubMed Web of Science ®Google Scholar
• Lu XL, Wang L, Chang SY, et al. Sonic Hedgehog Signaling Affected by Promoter Hypermethylation Induces Aberrant Gli2 Expression in Spina Bifida. Mol Neurobiol. 2016;53(8):5413–5424.
   PubMed Web of Science ®Google Scholar
• Wang L, Chang S, Wang Z, et al. Altered GNAS imprinting due to folic acid deficiency contributes to poor embryo development and may lead to neural tube defects. Oncotarget. 2017;8(67):110797–110810.
   PubMedGoogle Scholar
• Desbaillets I, Ziegler U, Groscurth P, et al. Embryoid bodies: an in vitro model of mouse embryogenesis. Exp Physiol. 2000;85(6):645–651.
   PubMed Web of Science ®Google Scholar
• O’Shea KS. Embryonic stem cell models of development. Anatomical Record. 1999;257(1):32–41.
   PubMedGoogle Scholar
• Kispert A, Koschorz B, Herrmann BG. The T protein encoded by Brachyury is a tissue-specific transcription factor. The EMBO Journal. 1995;14(19):4763–4772.
   PubMed Web of Science ®Google Scholar
• Valerie Wilson1 LM, Skarnes3 WC, Beddington1 RSP. The T gene is necessary for normal mesodermal morphogenetic cell movements during gastrulation. Development. 1995;121:877–886.
   PubMed Web of Science ®Google Scholar
• Pekkanen-Mattila M, Pelto-Huikko M, Kujala V, et al. Spatial and temporal expression pattern of germ layer markers during human embryonic stem cell differentiation in embryoid bodies. Histochem Cell Biol. 2010;133(5):595–606.
   PubMed Web of Science ®Google Scholar
• Marques CJ, Carvalho F, Sousa M, et al. Genomic imprinting in disruptive spermatogenesis. Lancet (London, England). 2004;363(9422):1700–1702.
   PubMed Web of Science ®Google Scholar
• Peng W, Chen Y, Luo X, et al. DNA methylation-associated repression of MEST/PEG1 expression contributes to the invasion of extravillous trophoblast cells. Placenta. 2016;46:92–101.
   PubMed Web of Science ®Google Scholar
• Kadota Y, Yanagawa M, Nakaya T, et al. Gene expression of mesoderm-specific transcript is upregulated as preadipocytes differentiate to adipocytes in vitro. J Physiol Sci. 2012;62(5):403–411.
   PubMed Web of Science ®Google Scholar
• Kimura-Yoshida C, Mochida K, Ellwanger K, et al. Fate Specification of Neural Plate Border by Canonical Wnt Signaling and Grhl3 is Crucial for Neural Tube Closure. EBioMedicine. 2015;2(6):513–527.
   PubMed Web of Science ®Google Scholar