Methylated DNA sequences in genomic imprinting.

No abstract is available for this paper.

• Publication year

  2000

• Venue

  Critical Reviews in Eukaryotic Gene Expression

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1615/CRITREVEUKARGENEEXPR.V10.I3-4.30PMID 11272467
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Alterations of DNA methylation patterns in germ cells and Sertoli cells from developing mouse testis

  2000cited by this paper
• Demethylation of the zygotic paternal genome.

  2000cited by this paper
• The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1

  2000cited by this paper
• Spatial Separation of Parental Genomes in Preimplantation Mouse Embryos

  2000cited by this paper
• Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome.

  2000cited by this paper
• The paternal methylation imprint of the mouse H19 locus is acquired in the gonocyte stage during foetal testis development

  2000cited by this paper
• Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype.

  2000cited by this paper
• A transcriptional insulator at the imprinted H19/Igf2 locus.

  2000cited by this paper
• Identification of a Methylation Imprint Mark within the Mouse Gnas Locus

  2000cited by this paper
• Organization and parent-of-origin-specific methylation of imprinted Peg3 gene on mouse proximal chromosome 7.

  2000cited by this paper
• H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19.

  2000cited by this paper
• De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

  2000cited by this paper
• Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

  2000cited by this paper
• Active demethylation of the paternal genome in the mouse zygote.

  2000cited by this paper
• Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function.

  2000cited by this paper
• An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus.

  2000cited by this paper
• CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

  2000cited by this paper
• Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch.

  2000cited by this paper
• Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome.

  2000cited by this paper
• Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive.

  2000cited by this paper
• Status of genomic imprinting in mouse spermatids.

  1999cited by this paper
• A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2.

  1999cited by this paper
• The imprinting box of the mouse Igf2r gene

  1999cited by this paper
• A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp

  1999cited by this paper
• A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome.

  1999cited by this paper
• The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.

  1999cited by this paper
• Molecular evolutionary evidence that H19 mRNA is functional.

  1999cited by this paper
• Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region.

  1999cited by this paper
• Imprinted methylation and its effect on expression of the mouse Zfp127 gene.

  1999cited by this paper
• Enhancer competition between H19 and Igf2 does not mediate their imprinting.

  1999cited by this paper
• Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation.

  1999cited by this paper
• Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome.

  1999cited by this paper
• A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region.

  1999cited by this paper
• Role of a 461-bp G-rich repetitive element in H19 transgene imprinting

  1999cited by this paper
• Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting center.

  1999cited by this paper
• In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit.

  1999cited by this paper
• Imprinting-mutation mechanisms in Prader-Willi syndrome.

  1999cited by this paper
• LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids.

  1999cited by this paper
• Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis.

  1999cited by this paper
• DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development.

  1999cited by this paper
• A direct repeat sequence at the Rasgrf1 locus and imprinted expression.

  1999cited by this paper
• The protein CTCF is required for the enhancer blocking activity of vertebrate insulators.

  1999cited by this paper
• Identification of imprinted loci by methylation-sensitive representational difference analysis: application to mouse distal chromosome 2.

  1999cited by this paper
• A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes.

  1999cited by this paper
• The DNA methylation paradox.

  1999cited by this paper
• A methylation imprint mark in the mouse imprinted gene Grf1/Cdc25Mm locus shares a common feature with the U2afbp-rs gene: an association with a short tandem repeat and a hypermethylated region.

  1998cited by this paper
• A Short DNA Methyltransferase Isoform Restores Methylation In Vivo *

  1998cited by this paper
• Location of enhancers is essential for the imprinting of H19 and Igf2 genes

  1998cited by this paper
• Influence of epigenetic changes during oocyte growth on nuclear reprogramming after nuclear transfer.

  1998cited by this paper
• Mutation analysis of UBE3A in Angelman syndrome patients.

  1998cited by this paper
• Sex-specific exons control DNA methyltransferase in mammalian germ cells.

  1998cited by this paper
• Igf2 imprinting does not require its own DNA methylation or H19 RNA.

  1998cited by this paper
• Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypes.

  1998cited by this paper
• Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

  1998cited by this paper
• The host defence function of genomic methylation patterns.

  1998cited by this paper
• Imprinting mechanisms.

  1998cited by this paper
• An oocyte-specific methylation imprint center in the mouse U2afbp-rs/U2af1-rs1 gene marks the establishment of allele-specific methylation during preimplantation development.

  1997cited by this paper
• The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

  1997cited by this paper
• Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans.

  1997cited by this paper
• Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.

  1997cited by this paper
• An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.

  1997cited by this paper
• De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

  1997cited by this paper
• A 5' differentially methylated sequence and the 3'-flanking region are necessary for H19 transgene imprinting

  1997cited by this paper
• The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse.

  1997cited by this paper
• The pre-implantation ontogeny of the H19 methylation imprint

  1997cited by this paper
• Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern.

  1997cited by this paper
• Mouse U2af1-rs1 is a neomorphic imprinted gene

  1997cited by this paper
• Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element.

  1997cited by this paper
• A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development

  1997cited by this paper
• The Mouse Necdin Gene Is Expressed from the Paternal Allele Only and Lies in the 7C Region of the Mouse Chromosome 7, a Region of Conserved Synteny to the Human Prader-Willi Syndrome Region

  1997cited by this paper
• Imprinted expression of the Igf2r gene depends on an intronic CpG island

  1997cited by this paper
• Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS–M

  1996cited by this paper
• Genetic and molecular analysis of the gypsy chromatin insulator of Drosophila.

  1996cited by this paper
• Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

  1996cited by this paper
• Absence of imprinting in U2AFBPL, a human homologue of the imprinted mouse gene U2afbp-rs.

  1996cited by this paper
• Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

  1996cited by this paper
• Creation of genomic methylation patterns

  1996cited by this paper
• Germ-line passage is required for establishment of methylation and expression patterns of imprinted but not of nonimprinted genes.

  1996cited by this paper
• Characterization of the imprinted IPW gene: allelic expression in normal and tumorigenic human tissues.

  1996cited by this paper
• Ubiquitous expression and imprinting of Snrpn in the mouse

  1995cited by this paper
• Development of normal mice from oocytes injected with secondary spermatocyte nuclei.

  1995cited by this paper
• A paternal–specific methylation imprint marks the alleles of the mouse H19 gene

  1995cited by this paper
• Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting.

  1995cited by this paper
• An enhancer deletion affects both H19 and Igf2 expression.

  1995cited by this paper
• Allele-specific replication timing in imprinted domains: absence of asynchrony at several loci.

  1995cited by this paper
• Disruption of imprinting caused by deletion of the H19 gene region in mice

  1995cited by this paper
• Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region.

  1995cited by this paper
• Characteristics of imprinted genes

  1995cited by this paper
• Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

  1995cited by this paper
• Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes.

  1994cited by this paper
• Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

  1994cited by this paper
• Genomic imprinting: lessons from mouse transgenes.

  1994cited by this paper
• New insights reveal complex mechanisms involved in genomic imprinting.

  1994cited by this paper
• Mice lackingSnrpn expression show normal regulation of neuronal alternative splicing events

  1994cited by this paper
• Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method

  1994cited by this paper
• Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

  1994cited by this paper
• Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting

  1994cited by this paper
• Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.

  1993cited by this paper
• Role for DNA methylation in genomic imprinting

  1993cited by this paper
• The ontogeny of allele‐specific methylation associated with imprinted genes in the mouse.

  1993cited by this paper

• Protein Interactions at Oxidized 5-Methylcytosine Bases.

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• 5-Methylcytosine and Its Oxidized Derivatives

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• Restoration of IGF2 imprinting by polycomb repressive complex 2 docking factor SUZ12 in colon cancer cells.

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• Promoter histone H3K27 methylation in the control of IGF2 imprinting in human tumor cell lines.

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• Promoter histone H 3 K 27 methylation in the control of IGF 2 imprinting in human tumor cell lines

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  2012cites this paper
• Genomic Imprinting

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• Biology and significance of signalling pathways activated by IGF-II

  2012influential citation
• Insights on imprinting from beyond mice and men.

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• Viability Assessment for Artificial Gametes: The Need for Biomarkers of Functional Competency1

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• Sex-Specific Dynamics of Global Chromatin Changes in Fetal Mouse Germ Cells

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• Interruption of intrachromosomal looping by CCCTC binding factor decoy proteins abrogates genomic imprinting of human insulin-like growth factor II

  2011influential citation
• Effects of endocrine disruptors on imprinted gene expression in the mouse embryo

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• RISC in Development; A Review on RNA Induced Silencing Complex and its Contribution to Cellular Differentiation

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• Allele-Specific H3K79 Di- versus Trimethylation Distinguishes Opposite Parental Alleles at Imprinted Regions

  2010cites this paper
• Epigenetic pre‐patterning and dynamics during initial stages of mammalian preimplantation development

  2010cites this paper
• CTCF-Dependent Chromatin Bias Constitutes Transient Epigenetic Memory of the Mother at the H19-Igf2 Imprinting Control Region in Prospermatogonia

  2010cites this paper
• Natural and artificial routes to pluripotency.

  2010cites this paper
• An in vitro ES cell imprinting model shows that imprinted expression of the Igf2r gene arises from an allele-specific expression bias

  2009cites this paper
• CTCF Regulates Allelic Expression of Igf2 by Orchestrating a Promoter-Polycomb Repressive Complex 2 Intrachromosomal Loop

  2008cites this paper
• Patterns of Hybrid Loss of Imprinting Reveal Tissue- and Cluster-Specific Regulation

  2008cites this paper
• The Human Genome Project

  2008cites this paper
• Parentally imprinted allele (PIA) typing in the differentially methylated region upstream of the human H19 gene.

  2008cites this paper
• RNA expression microarray analysis in mouse prospermatogonia: Identification of candidate epigenetic modifiers

  2008cites this paper
• Epigenetic mechanisms of gene regulation during mammalian spermatogenesis

  2008cites this paper
• An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs.

  2008cites this paper
• Monoallelic Expression of Multiple Genes in the CNS

  2007cites this paper
• Noncoding RNAs and intranuclear positioning in monoallelic gene expression.

  2007cites this paper
• Epigenetics—DNA-Based Mirror of our Environment?

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• Lsh controls silencing of the imprinted Cdkn1c gene

  2005cites this paper
• Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus

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• Tissue-specific and imprinted epigenetic modifications of the human NDN gene.

  2004cites this paper
• Transgenic animals in medicine: integration and expression of foreign genes, theoretical and applied aspects.

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• Genomic Imprinting in Mouse Embryonic Stem and Germ Cells

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• Parent-of-Origin-Specific Binding of Nuclear Hormone Receptor Complexes in the H19-Igf2 Imprinting Control Region

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• X chromosome inactivation, differentiation, and DNA methylation revisited, with a tribute to Susumu Ohno

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• Epigenetic regulation of Igf2/H19 imprinting at CTCF insulator binding sites

  2003cites this paper
• Novel paternity testing by distinguishing parental alleles at a VNTR locus in the differentially methylated region upstream of the human H19 gene.

  2003cites this paper
• Nucleosome positioning signals in the DNA sequence of the human and mouse H19 imprinting control regions.

  2003cites this paper
• Effects of methylation on expression of TMS1/ASC in human breast cancer cells

  2003cites this paper
• Nucleosome positioning signals and potential H-DNA within the DNA sequence of the imprinting control region of the mouse Igf2r gene.

  2003cites this paper
• Trans-HHS Workshop: Diet, DNA Methylation Processes and Health Maternal Methyl Supplements in Mice Affect Epigenetic Variation and DNA Methylation of Offspring

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• Maternal methyl supplements in mice affect epigenetic variation and DNA methylation of offspring.

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• Analysis of candidate imprinted genes linked to Dlk1-Gtl2 using a congenic mouse line

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• EDITORIAL Sobre la formación de términos técnicos

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