Disruption of imprinted X inactivation by parent-of-origin effects at Tsix

Cell

Volumn 103, Issue 1, 2000, Pages 17-27

  Lee, Jeannie T ^a,b  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME PROTEIN; PROTEIN TSIX; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GENE DISRUPTION; GENOTYPE; INTRAUTERINE GROWTH RETARDATION; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; X CHROMOSOME INACTIVATION;

ANIMALIA; EUTHERIA; MAMMALIA; METATHERIA;

EID: 0034730332     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(00)00101-X     Document Type: Article

References (57)

1. Derivation of embryonic stem cells
2. Epigenetic mechanisms underlying the imprinting of the mouse gene H19 gene
3. Double-stranded RNA as template for gene silencing
4. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
5. De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
6. The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus
7. A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome
8. The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus
9. XIST RNA paints the inactive X chromosome at interphase: Evidence for a novel RNA involved in nuclear/chromosome structure
10. Xce haplotypes show modified methylation in a region of the active X chromosome lying 3' to Xist
11. Functional analysis of the DXPas34 locus, a 3' regulator of Xist expression
12. Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
13. Maternally inherited X chromosome is not inactivated in mouse blastocysts due to parental imprinting
14. Mammals that break the rules: Genetics of marsupials and monotremes
15. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
16. Survival of X0 mouse fetuses: Effect of parental origin of the X chromosome or uterine environment
17. Retarded postimplantation development of XO mouse embryos: Impact of the parental origin of the monosomic X chromosome
18. Igf2 imprinting does not require its own DNA methylation or H19 RNA
19. DNA methylation stabilizes X chromosome inactivation in eutherians but not in marsupials: Evidence for multistep maintenance of mammalian X dosage compensation
20. Expression of Xist during mouse development suggests a role in the initiation of X chromosome inactivation
21. Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development
22. X chromosome imprinting and inactivation in the early mammalian embryo
23. Highly localized tracks of specific transcripts within interphase nuclei visualized by in situ hybridization
24. Long-range cis effects of ectopic X-inactivation centres on a mouse autosome
25. Targeted mutagenesis of Tsix leads to nonrandom X-inactivation
26. A 450 kb transgene displays properties of the mammalian X-inactivation center
27. Tsix, a gene antisense to Xist at the X-inactivation center
28. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
29. Role for DNA methylation in genomic imprinting
30. Gene action in the X chromosome of the mouse (Mus musculus L.)
31. Possible mechanisms of X chromosome inactivation
32. Xist-deficient mice are defective in dosage compensation but not spermatogenesis
33. X-chromosome inactivation mosaicism in the three germ layers and the germ line of the mouse embryo
34. Frequent derepression of G6PD and HPRT on the marsupial inactive X chromosome associated with cell proliferation in vitro
35. Sequential X chromosome inactivation coupled with cellular differentiation in early mouse embryos
36. Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2
37. Evolution of sex chromosomes in mammals
38. X chromosome inactivation is mediated by Xist RNA stabilization
39. Requirement for Xist in X chromosome inactivation
40. Timing of X-chromosome inactivation in postimplantation mouse embryos
41. Non-random X-chromosome in mouse X-autosome translocation embryos - Location of the inactivation centre
42. X-chromosome deletions in embryo-derived (EK) cell lines associated with lack of X-chromosome inactivation
43. An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript
44. Enhancer competition between H19 and Igf2 does not mediate their imprinting
45. Stabilization of Xist RNA mediate initiation of X chromosome inactivation
46. A maternally methylated CpG island in KVLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome
47. Ends Xist, but where are the beginnings?
48. Imprinting and the initiation of gene silencing in the germ line
49. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
50. Imprint switching for non-random X-chromosome inactivation during mouse oocyte growth
51. Preferential inactivation of the paternally derived X-chromosome in the extraembryonic membranes of the mouse
52. A paternally imprinted X chromosome retards the development of the ealry mouse embryo
53. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
54. The sins of the fathers and mothers: Genomic imprinting in mammalian development
55. Preferential expression of the maternally derived X chromosome in the mouse yolk sac
56. X chromosome inactivation, XIST, and pursuit of the X-inactivation center
57. Imprinted expression of the Igf2r gene depends on an intronic CpG island