Genetic conflict, genomic imprinting and establishment of the epigenotype in relation to growth

Reproduction

Volumn 122, Issue 2, 2001, Pages 185-193

  Moore, T ^a  

^a UNIVERSITY COLLEGE CORK   (Ireland)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; RNA;

ALLELE; CHROMATIN; CONTROLLED STUDY; CPG ISLAND; EMBRYO; EMBRYO DEVELOPMENT; EVOLUTION; FETUS DEVELOPMENT; GENE CLUSTER; GENE EXPRESSION; GENE LOCUS; GENETIC DISORDER; GENOME IMPRINTING; GENOTYPE; GERM LINE; GROWTH; GROWTH DISORDER; INTRON; MAMMAL; METHYLATION; NONHUMAN; PARENT; PATHOLOGY; PLANT; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; PROGENY; REVIEW; RNA TRANSCRIPTION; TANDEM REPEAT;

EID: 0034903768     PISSN: 14701626     EISSN: None     Source Type: Journal    
DOI: 10.1530/rep.0.1220185     Document Type: Review

References (71)

1. A skeletal muscle-specific mouse Igf2 repressor lies 40 kb downstream of the gene
2. Chromatin modification of imprinted H19 gene in mammalian spermatozoa
3. Embryonic inheritance of the chromatin organisation of the imprinted H19 domain in mouse spermatozoa
4. Epigenetic modifications necessary for normal development are established during oocyte growth in mice
5. Imprinting: A gamete's point of view
6. Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
7. Role of paternal and maternal genomes in mouse development
8. A silencer element identified in Drosophila is required for imprinting of H19 reporter transgenes in mice
9. Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome
10. Genomic imprinting in the mouse: Possible final analysis
11. Deletion of a silencer element in igf2 results in loss of imprinting independent of H19
12. Production of androgenetic zebrafish (Danio rerio)
13. The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development
14. Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo
15. Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch
16. Haploidy (androgenesis, gynogenesis, parthenogenesis)
17. Differential growth of the mouse preimplantation embryo in chemically defined media
18. Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes
19. Genomic imprinting in ruminants: Allele-specific gene expression in parthenogenetic sheep
20. Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: An introduction
21. The two-domain hypothesis in Beckwith-Wiedemann syndrome
22. Interference with DNA methyltransferase activity and genome methylation during F9 teratocarcinoma stem cell differentiation induced by polyamine depletion
23. Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: Implications for Beckwith-Wiedemann syndrome
24. Genomic imprinting and the theory of parent-offspring conflict Seminars in
25. Genetic conflicts and the private life of Peromyscus polionotus
26. Genomic imprinting and the strange case of the insulin-like growth factor II receptor
27. Parent-specific gene expression and the triploid endosperm
28. The genetical evolution of social behaviour I and II
29. Chromatin conformation of the H19 epigenetic mark
30. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
31. Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome
32. Growth effects of uniparental disomies and the conflict theory of genomic imprinting
33. Do we understand the evolution of genomic imprinting?
34. Imprinted genes have few and small introns
35. Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis
36. Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 gene
37. Epigenetic modifications during oocyte growth correlates with extended parthenogenetic development in the mouse
38. Effect of egg composition on the developmental capacity of androgenetic mouse embryos
39. An enhancer deletion affects both H19 and Igf2 expression
40. Genomic imprinting in mice: Its function and mechanism
41. An imprinting element from the mouse H19 locus functions as a silencer in Drosophila
42. Completion of mouse embryogenesis requires both the maternal and paternal genomes
43. Genomic imprinting of the insulin-like growth factor 2 gene in sheep
44. Molecular evolution of imprinted genes: No evidence for antagonistic coevolution
45. Evidence for a selectively favourable reduction in the mutation rate of the X chromosome
46. The evolution of genomic imprinting
47. From birds and bees to babies? Can theories on genetic conflict aid the clinician?
48. Genomic imprinting in mammalian development: A parental tug-of-war
49. Imprinting and monogamy
50. Genetic conflict in early development: Parental imprinting in normal and abnormal growth
51. Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2
52. Alterations of expression of developmentally important genes in preimplantation bovine embryos by in vitro culture conditions: Implications for subsequent development
53. Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis
54. Allelic expression of IGF2 in marsupials and birds
55. Active demethylation of the paternal genome in the mouse zygote
56. Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain
57. Enhancer competition between H19 and Igf2 does not mediate their imprinting
58. Aberrant fetal growth and development after in vitro culture of sheep zygotes
59. Genetic conflicts, multiple paternity and the evolution of genomic imprinting
60. Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour
61. Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function
62. Epigenotype switching of imprintable loci in embryonic germ cells
63. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
64. Parent-offspring conflict
65. The paternal methylation imprint of the mouse H19 locus is acquired in the gonocyte stage during foetal testis development
66. Genomic imprinting is disrupted in interspecific Peromyscus hybrids
67. Location of enhancers is essential for the imprinting of H19 and Igf2 genes
68. Embryonic and somatic cell cloning
69. Maternal epigenetics and methyl supplements affect agouti gene expression in Avy/a mice
70. Improving the safety of embryo technologies: Possible role of genomic imprinting
71. Large offspring syndrome in cattle and sheep