Home LiteratureArticle Details
PMID: 19201275 Published · ppublish English Journal Article Research Support, N.I.H., Intramural Review

Imprinting disorders and assisted reproductive technology.

Fertility and sterility ·Vol. 91 ·No. 2 ·2009-02-00 ·Pages 305-15

Manipalviratn S, DeCherney A, Segars J

Abstract

To review currently available literature on the association between imprinting disorders (Beckwith-Wiedemann syndrome [BWS], Angelman syndrome [AS] and retinoblastoma) and assisted reproductive technology (ART) in humans. Publications related to imprinting/epigenetic disorders including BWS, AS, and retinoblastoma with ART, as well as articles publishing outcome of ART, including IVF and ICSI from July 1978 to February 2008, were identified using PubMed, Medline, and EMBASE. Considerable evidence in animal studies has demonstrated alteration in gene imprinting of embryos cultured in vitro. Publications from Europe, the United States, and Australia have suggested an association between ART and BWS. Importantly, more than 90% of children with BWS that were born after ART had imprinting defects, compared with 40%-50% of children with BWS and conceived without ART. Moreover, there have been other reports suggesting an association between AS and ART. The majority of children with AS born after ART had an imprinting defect as the underlying etiology, specifically loss of methylation of the maternal allele. There was a single report suggesting an increased incidence of retinoblastoma in children conceived with ART. Because the absolute incidence of imprinting disorders is small (<1:12,000 births), routine screening for imprinting disorders in children conceived by ART is not recommended. Additional large cohort studies of children born after ART are needed to determine whether there is a genuine association between ART and imprinting disorders.

MeSH Terms
Angelman Syndrome/genetics Animals Beckwith-Wiedemann Syndrome/genetics DNA Methylation Evidence-Based Medicine Female Gene Expression Regulation, Developmental Genomic Imprinting Humans Pregnancy Reproductive Techniques, Assisted/adverse effects Retinoblastoma/genetics Risk Assessment Risk Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Manipalviratn Somjate
Reproductive Biology and Medicine Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA.
DeCherney Alan
Segars James
References (80)
80 references, click to expand
  1. 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 May;72(5):1338-41 PMID: 12772698
  2. Beckwith-Wiedemann syndrome, tumourigenesis and imprinting.
    Curr Opin Genet Dev. 1992 Jun;2(3):431-8 PMID: 1504618
  3. Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development.
    Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R61-8 PMID: 12668598
  4. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis.
    Nature. 1984 Apr 5-11;308(5959):548-50 PMID: 6709062
  5. Development of gynogenetic and parthenogenetic inner cell mass and trophectoderm tissues in reconstituted blastocysts in the mouse.
    J Embryol Exp Morphol. 1985 Dec;90:267-85 PMID: 3834032
  6. Intracytoplasmic sperm injection may increase the risk of imprinting defects.
    Am J Hum Genet. 2002 Jul;71(1):162-4 PMID: 12016591
  7. Exomphalos-macroglossia-gigantism syndrome in Jamaican infants.
    Am J Dis Child. 1970 Apr;119(4):316-21 PMID: 5434588
  8. Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma.
    Hum Genet. 1989 Sep;83(2):155-8 PMID: 2550354
  9. Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples.
    J Med Genet. 2005 Apr;42(4):289-91 PMID: 15805153
  10. Autism in Angelman syndrome: a population-based study.
    Pediatr Neurol. 1996 Feb;14(2):131-6 PMID: 8703225
  11. An enhancer deletion affects both H19 and Igf2 expression.
    Genes Dev. 1995 Sep 1;9(17):2079-89 PMID: 7544754
  12. Epigenetic decisions in mammalian germ cells.
    Science. 2007 Apr 20;316(5823):398-9 PMID: 17446388
  13. A survey of assisted reproductive technology births and imprinting disorders.
    Hum Reprod. 2007 Dec;22(12):3237-40 PMID: 17921133
  14. Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse.
    Genesis. 2003 Feb;35(2):88-93 PMID: 12533790
  15. Hypermethylation in the retinoblastoma gene is associated with unilateral, sporadic retinoblastoma.
    Cancer Genet Cytogenet. 1997 Oct 1;98(1):43-9 PMID: 9309117
  16. Role for DNA methylation in genomic imprinting.
    Nature. 1993 Nov 25;366(6453):362-5 PMID: 8247133
  17. Comparison of histone modifications in in vivo and in vitro fertilization mouse embryos.
    Biochem Biophys Res Commun. 2007 Mar 2;354(1):77-83 PMID: 17210126
  18. Imprinting diseases and IVF: Danish National IVF cohort study.
    Hum Reprod. 2005 Apr;20(4):950-4 PMID: 15665017
  19. Assisted Reproductive Technology affects developmental kinetics, H19 Imprinting Control Region methylation and H19 gene expression in individual mouse embryos.
    BMC Dev Biol. 2007 Oct 18;7:116 PMID: 17949482
  20. DNA methylation and mammalian epigenetics.
    Electrophoresis. 2001 Aug;22(14):2838-43 PMID: 11565778
  21. Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19.
    Am J Hum Genet. 2003 Jan;72(1):156-60 PMID: 12439823
  22. Methylation analysis of KvDMR1 in human oocytes.
    J Med Genet. 2007 Feb;44(2):144-7 PMID: 16950814
  23. Dynamics of DNA-demethylation in early mouse and rat embryos developed in vivo and in vitro.
    Mol Reprod Dev. 2007 Oct;74(10):1255-61 PMID: 17290422
  24. A census of mammalian imprinting.
    Trends Genet. 2005 Aug;21(8):457-65 PMID: 15990197
  25. Status of genomic imprinting in mouse spermatids.
    Hum Reprod. 1999 Apr;14(4):1050-6 PMID: 10221240
  26. Beckwith-Wiedemann syndrome.
    Am J Med Genet C Semin Med Genet. 2005 Aug 15;137C(1):12-23 PMID: 16010676
  27. Role of paternal and maternal genomes in mouse development.
    Nature. 1984 Sep 27-Oct 3;311(5984):374-6 PMID: 6482961
  28. The key to development: interpreting the histone code?
    Curr Opin Genet Dev. 2005 Apr;15(2):163-76 PMID: 15797199
  29. Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line.
    Genes Dev. 1992 May;6(5):705-14 PMID: 1577268
  30. Incidence of retinoblastoma in children born after in-vitro fertilisation.
    Lancet. 2003 Jan 25;361(9354):309-10 PMID: 12559867
  31. The imprinted gene and parent-of-origin effect database now includes parental origin of de novo mutations.
    Nucleic Acids Res. 2006 Jan 1;34(Database issue):D29-31 PMID: 16381868
  32. Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development.
    Hum Mol Genet. 2008 Jan 1;17(1):1-14 PMID: 17901045
  33. Aberrant methylation patterns at the two-cell stage as an indicator of early developmental failure.
    Mol Reprod Dev. 2002 Nov;63(3):329-34 PMID: 12237948
  34. Epigenetic reprogramming in mouse primordial germ cells.
    Mech Dev. 2002 Sep;117(1-2):15-23 PMID: 12204247
  35. A genome-wide analysis of CpG dinucleotides in the human genome distinguishes two distinct classes of promoters.
    Proc Natl Acad Sci U S A. 2006 Jan 31;103(5):1412-7 PMID: 16432200
  36. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene.
    Nature. 2000 May 25;405(6785):482-5 PMID: 10839546
  37. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development.
    Cell. 1999 Oct 29;99(3):247-57 PMID: 10555141
  38. Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes.
    Biol Reprod. 2001 Mar;64(3):918-26 PMID: 11207209
  39. Towards a molecular understanding of Prader-Willi and Angelman syndromes.
    Hum Mol Genet. 1999;8(10):1867-73 PMID: 10469839
  40. Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases.
    Clin Genet. 1994 Aug;46(2):168-74 PMID: 7820926
  41. Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo.
    Biol Reprod. 2000 Jun;62(6):1526-35 PMID: 10819752
  42. Genetic imprinting during impaired spermatogenesis.
    Mol Hum Reprod. 2006 Jun;12(6):407-11 PMID: 16608903
  43. Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.
    Hum Mol Genet. 2002 May 15;11(11):1317-25 PMID: 12019213
  44. Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients.
    Hum Mol Genet. 2007 Nov 1;16(21):2542-51 PMID: 17636251
  45. UBE3A/E6-AP mutations cause Angelman syndrome.
    Nat Genet. 1997 Jan;15(1):70-3 PMID: 8988171
  46. Beckwith-Wiedemann syndrome and IVF: a case-control study.
    Am J Hum Genet. 2004 Sep;75(3):526-8 PMID: 15284956
  47. Development of gynogenetic eggs in the mouse: implications for parthenogenetic embryos.
    Science. 1983 Dec 2;222(4627):1034-6 PMID: 6648518
  48. Monozygotic twinning and Wiedemann-Beckwith syndrome.
    Am J Med Genet. 1992 Feb 15;42(4):633-7 PMID: 1609846
  49. Genomic imprinting in disruptive spermatogenesis.
    Lancet. 2004 May 22;363(9422):1700-2 PMID: 15158633
  50. Chromatin in need of a fix: phosphorylation of H2AX connects chromatin to DNA repair.
    Mol Cell. 2005 Jun 10;18(6):617-22 PMID: 15949437
  51. Completion of mouse embryogenesis requires both the maternal and paternal genomes.
    Cell. 1984 May;37(1):179-83 PMID: 6722870
  52. Beckwith-Wiedemann syndrome and assisted reproduction technology (ART).
    J Med Genet. 2003 Jan;40(1):62-4 PMID: 12525545
  53. Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis.
    Development. 1998 Apr;125(8):1553-60 PMID: 9502736
  54. Epigenotype switching of imprintable loci in embryonic germ cells.
    Dev Genes Evol. 1998 Feb;207(8):551-61 PMID: 9510550
  55. Alterations of expression of developmentally important genes in preimplantation bovine embryos by in vitro culture conditions: implications for subsequent development.
    Theriogenology. 2000 Jan 1;53(1):21-34 PMID: 10735059
  56. Methylation-induced repression--belts, braces, and chromatin.
    Cell. 1999 Nov 24;99(5):451-4 PMID: 10589672
  57. Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culture.
    Nat Genet. 2001 Feb;27(2):153-4 PMID: 11175780
  58. Mechanisms of epigenetic inheritance.
    Curr Opin Cell Biol. 2007 Jun;19(3):266-72 PMID: 17466502
  59. Study of DNA-methylation patterns at chromosome 15q11-q13 in children born after ICSI reveals no imprinting defects.
    Mol Hum Reprod. 2000 Nov;6(11):1049-53 PMID: 11044469
  60. Tissue-specific effects of in vitro fertilization procedures on genomic cytosine methylation levels in overgrown and normal sized bovine fetuses.
    Biol Reprod. 2006 Jul;75(1):17-23 PMID: 16554415
  61. Epigenetics and the germline.
    Reproduction. 2005 Feb;129(2):137-49 PMID: 15695608
  62. In vitro fertilization (IVF) in Sweden: risk for congenital malformations after different IVF methods.
    Birth Defects Res A Clin Mol Teratol. 2005 Mar;73(3):162-9 PMID: 15678490
  63. Aberrant DNA methylation of imprinted loci in superovulated oocytes.
    Hum Reprod. 2007 Jan;22(1):26-35 PMID: 16923747
  64. Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection.
    Am J Hum Genet. 2003 Jan;72(1):218-9 PMID: 12549484
  65. Genomic imprinting: parental influence on the genome.
    Nat Rev Genet. 2001 Jan;2(1):21-32 PMID: 11253064
  66. Genomic imprinting and assisted reproductive technology: connections and potential risks.
    Semin Reprod Med. 2005 Aug;23(3):285-95 PMID: 16059835
  67. Epigenetic status of the H19 locus in human oocytes following in vitro maturation.
    Genomics. 2006 Mar;87(3):417-26 PMID: 16378710
  68. Assisted reproductive therapies and imprinting disorders--a preliminary British survey.
    Hum Reprod. 2006 Apr;21(4):1009-11 PMID: 16361294
  69. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus.
    Nature. 2000 May 25;405(6785):486-9 PMID: 10839547
  70. The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.
    EMBO J. 1993 Sep;12(9):3669-77 PMID: 7504628
  71. Epigenetic risks related to assisted reproductive technologies: risk analysis and epigenetic inheritance.
    Hum Reprod. 2002 Oct;17(10):2487-94 PMID: 12351517
  72. Transcriptional regulation by histone ubiquitination and deubiquitination.
    Genes Dev. 2003 Nov 15;17(22):2733-40 PMID: 14630937
  73. The DNA methyltransferases of mammals.
    Hum Mol Genet. 2000 Oct;9(16):2395-402 PMID: 11005794
  74. Infertility, assisted reproduction technologies and imprinting disturbances: a Dutch study.
    Hum Reprod. 2007 Sep;22(9):2476-80 PMID: 17586835
  75. Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients.
    Fertil Steril. 2005 Feb;83(2):349-54 PMID: 15705373
  76. Large offspring syndrome in cattle and sheep.
    Rev Reprod. 1998 Sep;3(3):155-63 PMID: 9829550
  77. Incidence and survival of retinoblastoma in The Netherlands: a register based study 1862-1995.
    Br J Ophthalmol. 1997 Jul;81(7):559-62 PMID: 9290369
  78. IVF results in de novo DNA methylation and histone methylation at an Igf2-H19 imprinting epigenetic switch.
    Mol Hum Reprod. 2005 Sep;11(9):631-40 PMID: 16219628
  79. The diverse functions of histone lysine methylation.
    Nat Rev Mol Cell Biol. 2005 Nov;6(11):838-49 PMID: 16261189
  80. Dynamic CpG and non-CpG methylation of the Peg1/Mest gene in the mouse oocyte and preimplantation embryo.
    J Biol Chem. 2005 May 20;280(20):20171-5 PMID: 15778220
Article Info
Journal
Fertility and sterility
Abbr.
Fertil Steril
ISSN
1556-5653
Published
2009-02-00
Pages
305-15
Language
English
Region
United States
NLM ID
0372772
PMCID
PMC3081604
Subset
IM
Grants
Intramural NIH HHS · Z01 HD008737-08 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]