Genomic imprinting: antagonistic mechanisms in the germ line and early embryo

scientific article

Genomic imprinting: antagonistic mechanisms in the germ line and early embryo is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

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P356DOI10.1101/SQB.2004.69.39
P8608Fatcat IDrelease_iw6a5pnfqrgblon2hbnvv5i4zm
P698PubMed publication ID16117631

P50authorMarisa S. BartolomeiQ85577670
P2093author name stringEngel NI
Fedoriw AM
P2860cites workDNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian developmentQ22010765
Parental imprinting of the mouse H19 geneQ22122365
A novel Dnmt3a isoform produced from an alternative promoter localizes to euchromatin and its expression correlates with active de novo methylationQ24302010
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 somaQ24531276
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 geneQ28145754
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locusQ28145756
Prader-Willi and Angelman syndromes: sister imprinted disordersQ28200133
Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprintingQ28508038
Windows for sex-specific methylation marked by DNA methyltransferase expression profiles in mouse germ cellsQ28511971
Role of CTCF binding sites in the Igf2/H19 imprinting control regionQ28512182
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1Q28589840
Transgenic RNAi reveals essential function for CTCF in H19 gene imprintingQ28590627
CTCF maintains differential methylation at the Igf2/H19 locusQ28593901
Role for DNA methylation in genomic imprintingQ29618669
Transcription of IAP endogenous retroviruses is constrained by cytosine methylationQ29618745
Mechanisms of genomic imprintingQ33632372
Active demethylation of the paternal genome in the mouse zygoteQ33901068
Dynamic reprogramming of DNA methylation in the early mouse embryo.Q34108785
Role of paternal and maternal genomes in mouse developmentQ34261845
Completion of mouse embryogenesis requires both the maternal and paternal genomesQ34267351
Genomic imprinting: intricacies of epigenetic regulation in clusters.Q34271454
Parental imprinting and human diseaseQ34412350
Genome organization, function, and imprinting in Prader-Willi and Angelman syndromesQ34433463
Primordial germ cells in the mouseQ35544665
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 domainsQ35964289
Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation patternQ36585144
Regulation of DNA methylation of Rasgrf1.Q37373945
A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulatorQ40747050
Imprinting in clusters: lessons from Beckwith-Wiedemann syndromeQ41566242
Sp1 elements protect a CpG island from de novo methylationQ42497349
Maternal primary imprinting is established at a specific time for each gene throughout oocyte growthQ43802401
The ubiquitin ligase Hyperplastic discs negatively regulates hedgehog and decapentaplegic expression by independent mechanismsQ47071133
CTCF elements direct allele-specific undermethylation at the imprinted H19 locusQ47383038
Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function.Q47590866
The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell developmentQ47811571
Organization and parent-of-origin-specific methylation of imprinted Peg3 gene on mouse proximal chromosome 7.Q47879943
Gene-specific timing and epigenetic memory in oocyte imprintingQ48004990
Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M.Q48060772
Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.Q48125063
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12.Q48231351
Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 geneQ48371609
Transgenic RNAi in mouse oocytes: a simple and fast approach to study gene functionQ48831302
Methylation dynamics of imprinted genes in mouse germ cells.Q48863844
Dnmt3L and the establishment of maternal genomic imprintsQ48874297
The paternal methylation imprint of the mouse H19 locus is acquired in the gonocyte stage during foetal testis developmentQ48886136
Antagonism between DNA hypermethylation and enhancer-blocking activity at the H19 DMD is uncovered by CpG mutations.Q52088468
Molecular biology. Mothers setting boundaries.Q52166844
Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis.Q52177094
Parental imprinting of the mouse insulin-like growth factor II gene.Q55052428
Epigenetic reprogramming in mouse primordial germ cellsQ57086629
P304page(s)39-45
P577publication date2004-01-01
P1433published inCold Spring Harbor Symposia on Quantitative BiologyQ15758412
P1476titleGenomic imprinting: antagonistic mechanisms in the germ line and early embryo
P478volume69

Reverse relations

cites work (P2860)
Q5313514711p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome.
Q40200248Conserved molecular portraits of bovine and human blastocysts as a consequence of the transition from maternal to embryonic control of gene expression
Q36065882Genomic imprinting and epigenetic control of development
Q37485567Male-Specific Transcription Factor Occupancy Alone Does Not Account for Differential Methylation at Imprinted Genes in the mouse Germ Cell Lineage.

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