Assisted Reproductive Technology affects developmental kinetics, H19 Imprinting Control Region methylation and H19gene expression in individual mouse embryos
Tóm tắt
Từ khóa
Tài liệu tham khảo
Schultz RM, Williams CJ: The science of ART. Science. 2002, 296: 2188-2190. 10.1126/science.1071741.
Bergh T, Ericson A, Hillensjo T, Nygren KG, Wennerholm UB: Deliveries and children born after in-vitro fertilisation in Sweden 1982-95: a retrospective cohort study. Lancet. 1999, 354: 1579-1585. 10.1016/S0140-6736(99)04345-7.
De Geyter C, De Geyter M, Steimann S, Zhang H, Holzgreve W: Comparative birth weights of singletons born after assisted reproduction and natural conception in previously infertile women. Hum Reprod. 2006, 21: 705-712. 10.1093/humrep/dei378.
Schieve LA, Meikle SF, Ferre C, Peterson HB, Jeng G, Wilcox LS: Low and very low birth weight in infants conceived with use of assisted reproductive technology. N Engl J Med. 2002, 346: 731-737. 10.1056/NEJMoa010806.
Bonduelle M, Wennerholm UB, Loft A, Tarlatzis BC, Peters C, Henriet S, Mau C, Victorin-Cederquist A, Van Steirteghem A, Balaska A, Emberson JR, Sutcliffe AG: A multi-centre cohort study of the physical health of 5-year-old children conceived after intracytoplasmic sperm injection, in vitro fertilization and natural conception. Hum Reprod. 2005, 20: 413-419. 10.1093/humrep/deh592.
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: 725-730. 10.1056/NEJMoa010035.
Wennerholm UB, Bergh C, Hamberger L, Lundin K, Nilsson L, Wikland M, Kallen B: Incidence of congenital malformations in children born after ICSI. Hum Reprod. 2000, 15: 944-948. 10.1093/humrep/15.4.944.
Van Steirteghem A, Bonduelle M, Devroey P, Liebaers I: Follow-up of children born after ICSI. Hum Reprod Update. 2002, 8: 111-116. 10.1093/humupd/8.2.111.
Stromberg B, Dahlquist G, Ericson A, Finnstrom O, Koster M, Stjernqvist K: Neurological sequelae in children born after in-vitro fertilisation: a population-based study. Lancet. 2002, 359: 461-465. 10.1016/S0140-6736(02)07674-2.
Kallen B, Finnstrom O, Nygren KG, Otterblad Olausson P: In vitro fertilization in Sweden: maternal characteristics. Acta Obstet Gynecol Scand. 2005, 84: 1185-1191. 10.1111/j.0001-6349.2005.00858.x.
Cox GF, Burger J, Lip V, Mau UA, Sperling K, Wu BL, Horsthemke B: Intracytoplasmic sperm injection may increase the risk of imprinting defects. Am J Hum Genet. 2002, 71: 162-164. 10.1086/341096.
DeBaun MR, Niemitz EL, Feinberg AP: Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19. Am J Hum Genet. 2003, 72: 156-160. 10.1086/346031.
Gicquel C, Gaston V, Mandelbaum J, Siffroi JP, Flahault A, Le Bouc Y: In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene. Am J Hum Genet. 2003, 72: 1338-1341. 10.1086/374824.
Ludwig H: Archives of Gynecology and Obstetrics: 135 years. Arch Gynecol Obstet. 2005, 271: 1-5. 10.1007/s00404-004-0711-1.
Maher ER, Brueton LA, Bowdin SC, Luharia A, Cooper W, Cole TR, Macdonald F, Sampson JR, Barratt CL, Reik W, Hawkins MM: Beckwith-Wiedemann syndrome and assisted reproduction technology (ART). J Med Genet. 2003, 40: 62-64. 10.1136/jmg.40.1.62.
Orstavik KH, Eiklid K, van der Hagen CB, Spetalen S, Kierulf K, Skjeldal O, Buiting K: Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection. Am J Hum Genet. 2003, 72: 218-219. 10.1086/346030.
Sutcliffe AG, Peters CJ, Bowdin S, Temple K, Reardon W, Wilson L, Clayton-Smith J, Brueton LA, Bannister W, Maher ER: Assisted reproductive therapies and imprinting disorders--a preliminary British survey. Hum Reprod. 2006, 21: 1009-1011. 10.1093/humrep/dei405.
Coan PM, Burton GJ, Ferguson-Smith AC: Imprinted genes in the placenta--a review. Placenta. 2005, 26 Suppl A: S10-20. 10.1016/j.placenta.2004.12.009.
Paulsen M, Ferguson-Smith AC: DNA methylation in genomic imprinting, development, and disease. J Pathol. 2001, 195: 97-110. 10.1002/path.890.
http://www.mgu.har.mrc.ac.uk/imprinting/imprinting.html. [http://www.mgu.har.mrc.ac.uk/research/imprinting/largemap.html]
Holmes R, Soloway PD: Regulation of imprinted DNA methylation. Cytogenet Genome Res. 2006, 113: 122-129. 10.1159/000090823.
Lewis A, Reik W: How imprinting centres work. Cytogenet Genome Res. 2006, 113: 81-89. 10.1159/000090818.
Reik W, Walter J: Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote. Nat Genet. 2001, 27: 255-256. 10.1038/85804.
Huntriss J, Daniels R, Bolton V, Monk M: Imprinted expression of SNRPN in human preimplantation embryos. Am J Hum Genet. 1998, 63: 1009-1014. 10.1086/302039.
Lighten AD, Hardy K, Winston RM, Moore GE: Expression of mRNA for the insulin-like growth factors and their receptors in human preimplantation embryos. Mol Reprod Dev. 1997, 47: 134-139. 10.1002/(SICI)1098-2795(199706)47:2<134::AID-MRD2>3.0.CO;2-N.
Monk M, Salpekar A: Expression of imprinted genes in human preimplantation development. Mol Cell Endocrinol. 2001, 183 Suppl 1: S35-40. 10.1016/S0303-7207(01)00575-5.
Geuns E, De Temmerman N, Hilven P, Van Steirteghem A, Liebaers I, De Rycke M: Methylation analysis of the intergenic differentially methylated region of DLK1-GTL2 in human. Eur J Hum Genet. 2007, 15: 352-361. 10.1038/sj.ejhg.5201759.
Geuns E, De Rycke M, Van Steirteghem A, Liebaers I: Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos. Hum Mol Genet. 2003, 12: 2873-2879. 10.1093/hmg/ddg315.
Doherty AS, Mann MR, Tremblay KD, Bartolomei MS, Schultz RM: Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo. Biol Reprod. 2000, 62: 1526-1535. 10.1095/biolreprod62.6.1526.
Sasaki H, Ferguson-Smith AC, Shum AS, Barton SC, Surani MA: Temporal and spatial regulation of H19 imprinting in normal and uniparental mouse embryos. Development. 1995, 121: 4195-4202.
Mann MR, Lee SS, Doherty AS, Verona RI, Nolen LD, Schultz RM, Bartolomei MS: Selective loss of imprinting in the placenta following preimplantation development in culture. Development. 2004, 131: 3727-3735. 10.1242/dev.01241.
Khosla S, Dean W, Brown D, Reik W, Feil R: Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes. Biol Reprod. 2001, 64: 918-926. 10.1095/biolreprod64.3.918.
Ecker DJ, Stein P, Xu Z, Williams CJ, Kopf GS, Bilker WB, Abel T, Schultz RM: Long-term effects of culture of preimplantation mouse embryos on behavior. Proc Natl Acad Sci U S A. 2004, 101: 1595-1600. 10.1073/pnas.0306846101.
Fernandez-Gonzalez R, Moreira P, Bilbao A, Jimenez A, Perez-Crespo M, Ramirez MA, Rodriguez De Fonseca F, Pintado B, Gutierrez-Adan A: Long-term effect of in vitro culture of mouse embryos with serum on mRNA expression of imprinting genes, development, and behavior. Proc Natl Acad Sci U S A. 2004, 101: 5880-5885. 10.1073/pnas.0308560101.
Li T, Vu TH, Ulaner GA, Littman E, Ling JQ, Chen HL, Hu JF, Behr B, Giudice L, Hoffman AR: IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch. Mol Hum Reprod. 2005, 11: 631-640. 10.1093/molehr/gah230.
Mann MR, Chung YG, Nolen LD, Verona RI, Latham KE, Bartolomei MS: Disruption of imprinted gene methylation and expression in cloned preimplantation stage mouse embryos. Biol Reprod. 2003, 69: 902-914. 10.1095/biolreprod.103.017293.
Tremblay KD, Saam JR, Ingram RS, Tilghman SM, Bartolomei MS: A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nat Genet. 1995, 9: 407-413. 10.1038/ng0495-407.
Tremblay KD, Duran KL, Bartolomei MS: A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development. Mol Cell Biol. 1997, 17: 4322-4329.
Olek A, Walter J: The pre-implantation ontogeny of the H19 methylation imprint. Nat Genet. 1997, 17: 275-276. 10.1038/ng1197-275.
Davis TL, Trasler JM, Moss SB, Yang GJ, Bartolomei MS: Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis. Genomics. 1999, 58: 18-28. 10.1006/geno.1999.5813.
Davis TL, Yang GJ, McCarrey JR, Bartolomei MS: The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development. Hum Mol Genet. 2000, 9: 2885-2894. 10.1093/hmg/9.19.2885.
Kanduri C, Pant V, Loukinov D, Pugacheva E, Qi CF, Wolffe A, Ohlsson R, Lobanenkov VV: Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive. Curr Biol. 2000, 10: 853-856. 10.1016/S0960-9822(00)00597-2.
Szabo P, Tang SH, Rentsendorj A, Pfeifer GP, Mann JR: Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function. Curr Biol. 2000, 10: 607-610. 10.1016/S0960-9822(00)00489-9.
Kaffer CR, Srivastava M, Park KY, Ives E, Hsieh S, Batlle J, Grinberg A, Huang SP, Pfeifer K: A transcriptional insulator at the imprinted H19/Igf2 locus. Genes Dev. 2000, 14: 1908-1919.
Srivastava M, Hsieh S, Grinberg A, Williams-Simons L, Huang SP, Pfeifer K: H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19. Genes Dev. 2000, 14: 1186-1195.
Thorvaldsen JL, Mann MR, Nwoko O, Duran KL, Bartolomei MS: Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting. Mol Cell Biol. 2002, 22: 2450-2462. 10.1128/MCB.22.8.2450-2462.2002.
Thorvaldsen JL, Duran KL, Bartolomei MS: Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Genes Dev. 1998, 12: 3693-3702.
Reese KJ, Bartolomei MS: Establishment and maintenance of H19 imprinting in the germline and preimplantation embryo. Cytogenet Genome Res. 2006, 113: 153-158. 10.1159/000090827.
Thorvaldsen JL, Fedoriw AM, Nguyen S, Bartolomei MS: Developmental profile of H19 differentially methylated domain (DMD) deletion alleles reveals multiple roles of the DMD in regulating allelic expression and DNA methylation at the imprinted H19/Igf2 locus. Mol Cell Biol. 2006, 26: 1245-1258. 10.1128/MCB.26.4.1245-1258.2006.
Ripoche MA, Kress C, Poirier F, Dandolo L: Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element. Genes Dev. 1997, 11: 1596-1604. 10.1101/gad.11.12.1596.
Gardner DK, Lane M: Alleviation of the '2-cell block' and development to the blastocyst of CF1 mouse embryos: role of amino acids, EDTA and physical parameters. Hum Reprod. 1996, 11: 2703-2712.
Ho Y, Wigglesworth K, Eppig JJ, Schultz RM: Preimplantation development of mouse embryos in KSOM: augmentation by amino acids and analysis of gene expression. Mol Reprod Dev. 1995, 41: 232-238. 10.1002/mrd.1080410214.
Biggers JD, McGinnis LK, Raffin M: Amino acids and preimplantation development of the mouse in protein-free potassium simplex optimized medium. Biol Reprod. 2000, 63: 281-293. 10.1095/biolreprod63.1.281.
Lane M, Gardner DK: Ammonium induces aberrant blastocyst differentiation, metabolism, pH regulation, gene expression and subsequently alters fetal development in the mouse. Biol Reprod. 2003, 69: 1109-1117. 10.1095/biolreprod.103.018093.
Fleming TP, Kwong WY, Porter R, Ursell E, Fesenko I, Wilkins A, Miller DJ, Watkins AJ, Eckert JJ: The embryo and its future. Biol Reprod. 2004, 71: 1046-1054. 10.1095/biolreprod.104.030957.
Houghton FD, Leese HJ: Metabolism and developmental competence of the preimplantation embryo. Eur J Obstet Gynecol Reprod Biol. 2004, 115 Suppl 1: S92-6. 10.1016/j.ejogrb.2004.01.019.
Hamatani T, Daikoku T, Wang H, Matsumoto H, Carter MG, Ko MS, Dey SK: Global gene expression analysis identifies molecular pathways distinguishing blastocyst dormancy and activation. Proc Natl Acad Sci U S A. 2004, 101: 10326-10331. 10.1073/pnas.0402597101.
Zeng F, Baldwin DA, Schultz RM: Transcript profiling during preimplantation mouse development. Dev Biol. 2004, 272: 483-496. 10.1016/j.ydbio.2004.05.018.
Wang QT, Piotrowska K, Ciemerych MA, Milenkovic L, Scott MP, Davis RW, Zernicka-Goetz M: A genome-wide study of gene activity reveals developmental signaling pathways in the preimplantation mouse embryo. Dev Cell. 2004, 6: 133-144. 10.1016/S1534-5807(03)00404-0.
Leighton PA, Ingram RS, Eggenschwiler J, Efstratiadis A, Tilghman SM: Disruption of imprinting caused by deletion of the H19 gene region in mice. Nature. 1995, 375: 34-39. 10.1038/375034a0.
Eggenschwiler J, Ludwig T, Fisher P, Leighton PA, Tilghman SM, Efstratiadis A: Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes. Genes Dev. 1997, 11: 3128-3142.
Reik W, Constancia M, Fowden A, Anderson N, Dean W, Ferguson-Smith A, Tycko B, Sibley C: Regulation of supply and demand for maternal nutrients in mammals by imprinted genes. J Physiol. 2003, 547: 35-44. 10.1113/jphysiol.2002.033274.
Reik W, Walter J: Genomic imprinting: parental influence on the genome. Nat Rev Genet. 2001, 2: 21-32. 10.1038/35047554.
Shamanski FL, Kimura Y, Lavoir MC, Pedersen RA, Yanagimachi R: Status of genomic imprinting in mouse spermatids. Hum Reprod. 1999, 14: 1050-1056. 10.1093/humrep/14.4.1050.
Warnecke PM, Mann JR, Frommer M, Clark SJ: Bisulfite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene. Genomics. 1998, 51: 182-190. 10.1006/geno.1998.5371.
Bock C, Reither S, Mikeska T, Paulsen M, Walter J, Lengauer T: BiQ Analyzer: visualization and quality control for DNA methylation data from bisulfite sequencing. Bioinformatics. 2005, 21: 4067-4068. 10.1093/bioinformatics/bti652.
http://www.universalprobelibrary.com. 2007, [http://www.universalprobelibrary.com]