(Q35088684)

6 August 2017

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title

Molecular links between X-inactivation and autosomal imprinting: X-inactivation as a driving force for the evolution of imprinting? (English)

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6 August 2017

Jeannie T Lee

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6 August 2017

language of work or name

English

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publication date

1 March 2003

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6 August 2017

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6 August 2017

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6 August 2017

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6 August 2017

page(s)

R242-54

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Intergenic transcription and developmental remodeling of chromatin subdomains in the human beta-globin locus.

6 August 2017

cites work

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7 January 2021

Nascent pre-mRNA transcripts are associated with nuclear regions enriched in splicing factors

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7 January 2021

DPY-27:a chromosome condensation protein homolog that regulates C. elegans dosage compensation through association with the X chromosome

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7 January 2021

Monoallelic expression: 'there can only be one'

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7 January 2021

X-chromosome inactivation: counting, choice and initiation

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7 January 2021

Forty years of decoding the silence in X-chromosome inactivation

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7 January 2021

Imprinted X inactivation in eutherians: a model of gametic execution and zygotic relaxation

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7 January 2021

Genomic imprinting: parental influence on the genome

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Gene action in the X-chromosome of the mouse (Mus musculus L.)

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7 January 2021

Localization of the X inactivation centre on the human X chromosome in Xq13.

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7 January 2021

A 450 kb transgene displays properties of the mammalian X-inactivation center.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Xist yeast artificial chromosome transgenes function as X-inactivation centers only in multicopy arrays and not as single copies

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Late DNA Replication in the Paternally Derived X Chromosome of Female Kangaroos

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7 January 2021

Inheritance of glucose-6-phosphate dehydrogenase variation in kangaroos

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7 January 2021

Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Preferential expression of the maternally derived X chromosome in the mouse yolk sac

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Requirement for Xist in X chromosome inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Xist-deficient mice are defective in dosage compensation but not spermatogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Tsix, a gene antisense to Xist at the X-inactivation centre

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Targeted mutagenesis of Tsix leads to nonrandom X inactivation.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

A functional role for Tsix transcription in blocking Xist RNA accumulation but not in X-chromosome choice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Antisense transcription through the Xist locus mediates Tsix function in embryonic stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Completion of mouse embryogenesis requires both the maternal and paternal genomes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Genomic imprinting in mammals.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Parental imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Towards a molecular understanding of Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

A first-generation X-inactivation profile of the human X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Imprinted expression of the Igf2r gene depends on an intronic CpG island.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The non-coding Air RNA is required for silencing autosomal imprinted genes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Enox, a novel gene that maps 10 kb upstream of Xist and partially escapes X inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Chromosomal silencing and localization are mediated by different domains of Xist RNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

X-chromosome inactivation: closing in on proteins that bind Xist RNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

X-chromosome inactivation and the search for chromosome-wide silencers

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Histone macroH2A1 is concentrated in the inactive X chromosome of female mammals

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Mitotically stable association of polycomb group proteins eed and enx1 with the inactive x chromosome in trophoblast stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Characterization and quantitation of differential Tsix transcripts: implications for Tsix function

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The DNA methyltransferases of mammals

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Chromatin modification and epigenetic reprogramming in mammalian development

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Role for DNA methylation in genomic imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Dnmt3L and the establishment of maternal genomic imprints

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

A global disorder of imprinting in the human female germ line

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Gamete-specific methylation correlates with imprinting of the murine Xist gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Methylation of the mouse Xist gene in sperm and eggs correlates with imprinted Xist expression and paternal X-inactivation.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Loss of methylation activates Xist in somatic but not in embryonic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

DNA hypomethylation can activate Xist expression and silence X-linked genes.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

X Inactivation in the Mouse Embryo Deficient for Dnmt1: Distinct Effect of Hypomethylation on Imprinted and Random X Inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Mapping the murine Xce locus with (CA)n repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Methylation profiles of DXPas34 during the onset of X-inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

CTCF, a candidate trans-acting factor for X-inactivation choice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Homozygous Tsix mutant mice reveal a sex-ratio distortion and revert to random X-inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Polar overdominance at the ovine callipyge locus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Homologous association of oppositely imprinted chromosomal domains

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The nucleotides responsible for the direct physical contact between the chromatin insulator protein CTCF and the H19 imprinting control region manifest parent of origin-specific long-distance insulation and methylation-free domains

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

CTCF maintains differential methylation at the Igf2/H19 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Xce haplotypes show modified methylation in a region of the active X chromosome lying 3' to Xist

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The many faces of histone lysine methylation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Histone H3 lysine 9 methylation is an epigenetic imprint of facultative heterochromatin.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Methylation of histone H3 at Lys-9 is an early mark on the X chromosome during X inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Histone H3 lysine 9 methylation occurs rapidly at the onset of random X chromosome inactivation.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

The imprinting mechanism of the Prader-Willi/Angelman regional control center

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Imprinted X inactivation maintained by a mouse Polycomb group gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Role of histone H3 lysine 27 methylation in Polycomb-group silencing

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Histone methyltransferase activity of a Drosophila Polycomb group repressor complex

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal Polycomb sites

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Histone methyltransferase activity associated with a human multiprotein complex containing the Enhancer of Zeste protein

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

BRCA1 supports XIST RNA concentration on the inactive X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

M6P/IGF2R imprinting evolution in mammals

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Monotreme IGF2 expression and ancestral origin of genomic imprinting

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Genomic imprinting--defusing the ovarian time bomb

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

DNA methylation and imprinting: why bother?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Sex Specific X Chromosome Expression Caused by Genomic Imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Did genomic imprinting and X chromosome inactivation arise from stochastic expression?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Imprinting and X-chromosome inactivation.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Mammals that break the rules: genetics of marsupials and monotremes

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https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

X-inactivation in marsupials and monotremes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

Model for evolution of Y chromosomes and dosage compensation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900162-3

7 January 2021

10.1016/S0960-9822(03)00162-3

Identifiers

DOI

1 reference

6 August 2017

1 reference