Minireview: Parthenogenesis in mammals

Molecular Reproduction and Development

Volumn 59, Issue 4, 2001, Pages 468-474

  Rougier, Nathalie ^a   Werb, Zena ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSTATIC AGENT; DNA; MITOGEN ACTIVATED PROTEIN KINASE; RNA;

CPG ISLAND; DIPLOIDY; DNA METHYLATION; EMBRYO DEVELOPMENT; GENE EXPRESSION; HAPLOIDY; MAMMAL; MEIOSIS; NONHUMAN; PARTHENOGENESIS; PATHOGENESIS; POLYPLOIDY; PRIORITY JOURNAL; SHORT SURVEY;

ANIMALS; FEMALE; GENOME; GENOMIC IMPRINTING; MALE; MAMMALS; MITOGEN-ACTIVATED PROTEIN KINASES; OVUM; PARTHENOGENESIS;

MAMMALIA;

EID: 0034962157     PISSN: 1040452X     EISSN: None     Source Type: Journal    
DOI: 10.1002/mrd.1054     Document Type: Short Survey

References (80)

1. MAPK inactivation is required for the G2 to M-phase transition of the first mitotic cell cycle
2. CpG islands as genomic footprints of promoters that are associated with replication origins
3. Competition - A common motif for the imprinting mechanism?
4. Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
5. Role of paternal and maternal genomes in mouse development
6. Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells. The carboxyl-terminal domain of the mammalian enzymes is related to bacterial restriction methyltransferases
7. De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
8. The imprinting box of the mouse Igf2r gene
9. The ontogeny of allele-specific methylation associated with imprinted genes in the mouse
10. Mechanisms of genomic imprinting
11. DNA methyltransferase is actively retained in the cytoplasm during early development
12. Specific Alu binding protein from human sperm chromatin prevents DNA methylation
13. The Mos/mitogen-activated protein kinase (MAPK) pathway regulates the size and degradation of the first polar body in maturing mouse oocytes
14. The development potential of parthenogenetically derived cells in chimeric mouse embryos: Implications for action of imprinted genes
15. Disruption of c-mos causes parthenogenetic development of unfertilized mouse eggs
16. Imprinting mechanisms
17. Chromosome inheritance and the problem of chromosome 'imprinting' in Sciara (Sciaridae, Diptera)
18. DNA methyltransferase Dnmt1 associates with histone deacetylase activity
19. Suppression of DNA replication via Mos function during meiotic divisions in Xenopus oocytes
20. Genomic imprinting and the strange case of the insulin-like growth factor II receptor
21. Parthenogenetic activation of oocytes in c-mos-deficient mice
22. Methylation levels of maternal and paternal genomes during preimplantation development
23. Do we understand the evolution of genomic imprinting?
24. The conflict theory of genomic imprinting: How much can be explained?
25. Parthenogenetic stem cells in postnatal mouse chimeras
26. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
27. Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line
28. Allele-specific replication timing of imprinted gene regions
29. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region
30. Mouse embryonic germ (EG) cell lines: Transmission through the germline and differences in the methylation imprint of insulin-like growth factor 2 receptor (Igf2r) gene compared with embryonic stem (ES) cell lines
31. Homologous association of oppositely imprinted chromosomal domains
32. Igf2r and Igf2 gene expression in androgenetic, gynogenetic, and parthenogenetic preimplantation mouse embryos: Absence of regulation by genomic imprinting
33. Genetic variation in trophectoderm function in parthenogenetic mouse embryos
34. Genetic dissection of susceptibility to murine ovarian teratomas that originate from parthenogenetic oocytes
35. Role for DNA methylation in genomic imprinting
36. Genomic imprinting and position-effect variegation in Drosophila melanogaster
37. Identification of genes showing altered expression in preimplantation and early postimplantation parthenogenetic embryos
38. Parthenogenetic activation of marmoset (Callithrix jacchus) oocytes and the development of marmoset parthenogenones in vitro and in vivo
39. Sex-specific exons control DNA methyltransferase in mammalian germ cells
40. Parthenogenesis
41. Normal development but differentially altered proliferative responses of lymphocytes in mice lacking CD81
42. Temporal and regional changes in DNA methylation in the embryonic, extraembryonic, and germ cell lineages during mouse embryo development
43. Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
44. Stem cell defects in parthenogenetic peri-implantation embryos
45. Functional analysis of trophoblast giant cells in parthenogenetic mouse embryos
46. DNA methylation and chromatin modification
47. Dnmt2 is not required for de novo and maintenance methylation of viral DNA in embryonic stem cells
48. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
49. Active demethylation of the paternal genome in the mouse zygote
50. Insulin-like growth factor II acts through an endogenous growth pathway regulated by imprinting in early mouse embryos
51. DNA methylation and embryogenesis
52. Imprinting mechanisms in mammals
53. Chromosome methylation patterns during mammalian preimplantation development
54. Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse
55. Enhancer competition between H19 and Igf2 does not mediate their imprinting
56. The Dlk1 and Gtl2 genes are linked and reciprocally imprinted
57. In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit
58. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
59. DNA methylation represses transcription in vivo
60. Asynchronous replication of imprinted genes is established in the gametes and maintained during development
61. The uniqueness of the imprinting mechanism
62. Genetic conflicts, multiple paternity and the evolution of genomic imprinting
63. Defective chorioallantoic fusion in mid-gestation lethality of parthenogenonetetraploid chimeras
64. The development of teratomas from parthenogenetically activated ovarian mouse eggs
65. A human parthenogenetic chimaera
66. Abnormal development of embryonic and extraembryonic cell lineages in parthenogenetic mouse embryos
67. Chromosomal status of uni-pronuclear human zygotes following invitro fertilization and intracytoplasmic sperm injection
68. Expression and methylation of imprinted genes during in vitro differentiation of mouse parthenogenetic and androgenetic embryonic stem cell lines
69. Biallelic expression of imprinted genes in the mouse germ line: Implications for erasure, establishment, and mechanisms of genomic imprinting
70. Early development and X-chromosome inactivation in mouse parthenogenetic embryos
71. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
72. Germ-line passage is required for establishment of methylation and expression patterns of imprinted but not of nonimprinted genes
73. Cell proliferation is reduced in parthenogenetic mouse embryos at the blastocyst stage: A quantitative study
74. The non-viability of uniparental mouse conceptuses correlates with the loss of the products of imprinted genes
75. Bisulfite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene
76. Transcriptional control: Imprinting insulation
77. Imprinted expression of the Igf2r gene depends on an intronic CpG island
78. A candidate mammalian DNA methyltransferase related to pmt1p of fission yeast
79. DNA (cytosine-5)-methyltransferases in mouse cells and tissues. Studies with a mechanism-based probe