Maintaining memory of silencing at imprinted differentially methylated regions

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Maintaining memory of silencing at imprinted differentially methylated regions is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1000070031
P356DOI10.1007/S00018-016-2157-6
P932PMC publication ID4819931
P698PubMed publication ID26883803
P5875ResearchGate publication ID294919595

P50authorHsiao Phin Joanna VoonQ80310067
Richard J GibbonsQ37830276
P2093author name stringRichard J Gibbons
Hsiao P J Voon
P2860cites workGenome-wide analysis of KAP1 binding suggests autoregulation of KRAB-ZNFsQ21563454
The ATRX-ADD domain binds to H3 tail peptides and reads the combined methylation state of K4 and K9Q24297608
Histone H3.1 and H3.3 complexes mediate nucleosome assembly pathways dependent or independent of DNA synthesisQ24304348
KDM1B is a histone H3K4 demethylase required to establish maternal genomic imprintsQ24312768
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57Q24312925
A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprintsQ24322379
Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genesQ24539228
Genome-wide maps of chromatin state in pluripotent and lineage-committed cellsQ24632506
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeQ24644175
DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNAQ24645346
The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferaseQ24678267
An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locusQ24678820
SETDB1: a novel KAP-1-associated histone H3, lysine 9-specific methyltransferase that contributes to HP1-mediated silencing of euchromatic genes by KRAB zinc-finger proteinsQ24685694
Spotting the enemy within: Targeted silencing of foreign DNA in mammalian genomes by the Krüppel-associated box zinc finger protein familyQ26782206
New insights into establishment and maintenance of DNA methylation imprints in mammalsQ26852971
Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatinQ27670415
ATRX ADD domain links an atypical histone methylation recognition mechanism to human mental-retardation syndromeQ27670417
Structure of the variant histone H3.3–H4 heterodimer in complex with its chaperone DAXXQ27675056
Methylation of histone H3 lysine 9 creates a binding site for HP1 proteinsQ27860456
Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domainQ27860477
Set2 methylation of histone H3 lysine 36 suppresses histone exchange on transcribed genesQ27929868
Histone H3 methylation by Set2 directs deacetylation of coding regions by Rpd3S to suppress spurious intragenic transcriptionQ27932406
ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cellsQ28114801
Epigenetic regulation of telomere length in mammalian cells by the Suv39h1 and Suv39h2 histone methyltransferasesQ51598430
Imprinted expression of the Igf2r gene depends on an intronic CpG islandQ52192434
Epigenetic reprogramming in mouse primordial germ cellsQ57086629
HIRA Is Critical for a Nucleosome Assembly Pathway Independent of DNA SynthesisQ57549500
Demethylation of the zygotic paternal genomeQ59066150
Mitochondria and the death of oocytesQ59075483
Airn transcriptional overlap, but not its lncRNA products, induces imprinted Igf2r silencingQ85652146
Histone tails regulate DNA methylation by allosterically activating de novo methyltransferase.Q35348766
In embryonic stem cells, ZFP57/KAP1 recognize a methylated hexanucleotide to affect chromatin and DNA methylation of imprinting control regionsQ35534127
In vivo targeting of de novo DNA methylation by histone modifications in yeast and mouse.Q35545732
Zinc finger protein ZFP57 requires its co-factor to recruit DNA methyltransferases and maintains DNA methylation imprint in embryonic stem cells via its transcriptional repression domainQ35694053
Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expressionQ35819244
Global profiling of DNA methylation erasure in mouse primordial germ cellsQ35864711
A unique regulatory phase of DNA methylation in the early mammalian embryoQ35903352
Genome-wide bisulfite sequencing in zygotes identifies demethylation targets and maps the contribution of TET3 oxidation.Q35973407
The KRAB-ZFP/KAP1 system contributes to the early embryonic establishment of site-specific DNA methylation patterns maintained during developmentQ36915286
SetDB1 contributes to repression of genes encoding developmental regulators and maintenance of ES cell stateQ37426752
Defending the genome from the enemy within: mechanisms of retrotransposon suppression in the mouse germlineQ37698311
DAXX co-folds with H3.3/H4 using high local stability conferred by the H3.3 variant recognition residuesQ37701297
Genomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylationQ38918003
Distinctive chromatin in human sperm packages genes for embryo developmentQ40137854
Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.Q40540300
Repressive and active histone methylation mark distinct promoters in human and mouse spermatozoaQ46329417
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12.Q48231351
Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatinQ28187783
A mouse model for Prader-Willi syndrome imprinting-centre mutationsQ28271033
Distinct factors control histone variant H3.3 localization at specific genomic regionsQ28275277
PGC7/Stella protects against DNA demethylation in early embryogenesisQ28506319
The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatinQ28506981
PGC7 binds histone H3K9me2 to protect against conversion of 5mC to 5hmC in early embryosQ28508667
Histone H3-K9 methyltransferase ESET is essential for early developmentQ28513000
KDM5B regulates embryonic stem cell self-renewal and represses cryptic intragenic transcriptionQ28513535
Reprogramming of the paternal genome upon fertilization involves genome-wide oxidation of 5-methylcytosineQ28585429
Identification of PGC7, a new gene expressed specifically in preimplantation embryos and germ cellsQ28589532
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1Q28589840
The role of Tet3 DNA dioxygenase in epigenetic reprogramming by oocytesQ28595016
DAXX envelops a histone H3.3-H4 dimer for H3.3-specific recognitionQ28658254
Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulationQ29614333
Partitioning and plasticity of repressive histone methylation states in mammalian chromatinQ29614513
Histone H3 lysine 4 methylation patterns in higher eukaryotic genesQ29614678
The histone variant H3.3 marks active chromatin by replication-independent nucleosome assemblyQ29618256
Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stabilityQ29620365
Allelome.PRO, a pipeline to define allele-specific genomic features from high-throughput sequencing data.Q30982170
Identifying genes preferentially expressed in undifferentiated embryonic stem cellsQ33295361
Regulation of DNA methylation turnover at LTR retrotransposons and imprinted loci by the histone methyltransferase Setdb1Q33606891
Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome.Q33760054
The function of non-coding RNAs in genomic imprintingQ33761870
Characterization of the contradictory chromatin signatures at the 3' exons of zinc finger genesQ33828243
Relationship between Gene Body DNA Methylation and Intragenic H3K9me3 and H3K36me3 Chromatin MarksQ33883693
The Dnmt3a PWWP domain reads histone 3 lysine 36 trimethylation and guides DNA methylationQ34074317
Transcription Is Required to Establish Maternal Imprinting at the Prader-Willi Syndrome and Angelman Syndrome LocusQ34126322
Dynamic chromatin modifications characterise the first cell cycle in mouse embryos.Q34402750
ATRX Plays a Key Role in Maintaining Silencing at Interstitial Heterochromatic Loci and Imprinted Genes.Q34471329
Histone H3.3 is required for endogenous retroviral element silencing in embryonic stem cellsQ34474887
Histone variant H3.3 provides the heterochromatic H3 lysine 9 tri-methylation mark at telomeresQ34490850
Epigenetic events in mammalian germ-cell development: reprogramming and beyondQ34736397
Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation.Q35077074
Dynamic CpG island methylation landscape in oocytes and preimplantation embryosQ35135165
The KRAB zinc finger protein ZFP809 is required to initiate epigenetic silencing of endogenous retrovirusesQ35173298
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.Q35211749
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue9
P407language of work or nameEnglishQ1860
P921main subjectcell biologyQ7141
regulation of gene expressionQ411391
gene silencingQ1431332
P304page(s)1871-1879
P577publication date2016-05-01
P13046publication type of scholarly workreview articleQ7318358
P1433published inCellular and Molecular Life SciencesQ5058352
P1476titleMaintaining memory of silencing at imprinted differentially methylated regions
P478volume73

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cites work (P2860)
Q39432488Do social insects support Haig's kin theory for the evolution of genomic imprinting?
Q30234309Epigenetic Control of Human Endogenous Retrovirus Expression: Focus on Regulation of Long-Terminal Repeats (LTRs)
Q64260073How Does Reprogramming to Pluripotency Affect Genomic Imprinting?
Q40292496Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome
Q28067042The effect of exposure to nanoparticles and nanomaterials on the mammalian epigenome
Q38805744Transposable elements: Self-seekers of the germline, team-players of the soma

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