Methylation dynamics of imprinted genes in mouse germ cells

Genomics

Volumn 79, Issue 4, 2002, Pages 530-538

  Lucifero, Diana ^a   Mertineit, Carmen ^a   Clarke, Hugh J ^a   Bestor, Timothy H ^b   Trasler, Jacquetta M ^c  

^a RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^b ROYAL VICTORIA HOSPITAL   (Canada)

^c Surgeons of Columbia University ^*  (United States)

Author keywords

DNA methylation; Epigenetic; Genomic imprinting; H19; Igf2r; Mest; Mouse; Oocyte; Peg3; Snrpn; Sperm

Indexed keywords

ALLELE; ANIMAL CELL; ARTICLE; CATALYSIS; CELL MATURATION; GENOME IMPRINTING; GERM CELL; INTRON; MEIOSIS; METAPHASE; METHYLATION; MOLECULAR DYNAMICS; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE DEVELOPMENT; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; TRANSCRIPTION REGULATION;

ANIMALIA; MAMMALIA; RODENTIA;

EID: 0036205914     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2002.6732     Document Type: Article

References (37)

1. Role for DNA methylation in genomic imprinting
2. Transcription of IAP endogenous retroviruses is constrained by cytosine methylation
3. Cytosine methylation and mammalian development
4. The DNA methyltransferases of mammals
5. Targeted mutation of the DNA methyl-transferase gene results in embryonic lethality
6. Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development
7. Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis
8. The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development
9. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
10. Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal
11. Genomic structure and parent-of-origin-specific methylation of Peg1
12. Organization and parent-of origin methylation of imprinted Peg3 gene on mouse proximal chromosome 7
13. De novo deletions of SNRPN exon 1 in early human and mouse embryos result in paternal to maternal imprint switch
14. Loss of the imprinted IGF2/cation independent mannose-6-phosphate receptor results in fetal overgrowth and perinatal lethality
15. Epigenetic changes in IGF2R is associated with fetal overgrowth after sheep embryo culture
16. Abnormal maternal behavior and offspring growth retardation associated with loss of the imprinted gene Mest
17. Regulation of maternal behavior and offspring growth by paternally expressed Peg3
18. Imprinted segments in the human genome: Different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method
19. A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development
20. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
21. CTCF mediates methylation-sensitive enhancer-blocking actiity at the H19/Igf2 locus
22. Epigenetic modifications necessary for normal development are established during oocyte growth in mice
23. The ontogeny of allele-specific methylation associated with imprinted genes in the mouse
24. Epigenetic modifications during oocyte growth correlates with extended parthenogenetic development in the mouse
25. Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis
26. Parental methylation patterns of a transgenic locus in adult somatic tissues are imprinted during gametogenesis
27. Disruption in primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis
28. Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse
29. Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line
30. The pre-implantation ontogeny of the H19 methylation imprint
31. Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene
32. Mitochondrial gene expression in male germ cells of the mouse
33. Isolation and culture of oocytes
34. The developmental capacity of mouse oocytes that matured spontaneously in vitro is normal
35. Suppression of chromosome condensation during meiotic maturation induces parthenogenetic development of mouse oocytes
36. Bisulfite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene