607 related articles for article (PubMed ID: 31485078)
1. The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscape.
Weinberg DN; Papillon-Cavanagh S; Chen H; Yue Y; Chen X; Rajagopalan KN; Horth C; McGuire JT; Xu X; Nikbakht H; Lemiesz AE; Marchione DM; Marunde MR; Meiners MJ; Cheek MA; Keogh MC; Bareke E; Djedid A; Harutyunyan AS; Jabado N; Garcia BA; Li H; Allis CD; Majewski J; Lu C
Nature; 2019 Sep; 573(7773):281-286. PubMed ID: 31485078
[TBL] [Abstract][Full Text] [Related]
2. H3K36me2/3 Binding and DNA Binding of the DNA Methyltransferase DNMT3A PWWP Domain Both Contribute to its Chromatin Interaction.
Dukatz M; Holzer K; Choudalakis M; Emperle M; Lungu C; Bashtrykov P; Jeltsch A
J Mol Biol; 2019 Dec; 431(24):5063-5074. PubMed ID: 31634469
[TBL] [Abstract][Full Text] [Related]
3. Histone H3K36me2 and H3K36me3 form a chromatin platform essential for DNMT3A-dependent DNA methylation in mouse oocytes.
Yano S; Ishiuchi T; Abe S; Namekawa SH; Huang G; Ogawa Y; Sasaki H
Nat Commun; 2022 Aug; 13(1):4440. PubMed ID: 35922445
[TBL] [Abstract][Full Text] [Related]
4. NSD1 deposits histone H3 lysine 36 dimethylation to pattern non-CG DNA methylation in neurons.
Hamagami N; Wu DY; Clemens AW; Nettles SA; Li A; Gabel HW
Mol Cell; 2023 May; 83(9):1412-1428.e7. PubMed ID: 37098340
[TBL] [Abstract][Full Text] [Related]
5. DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancer.
Watanabe H; Higashimoto K; Miyake N; Morita S; Horii T; Kimura M; Suzuki T; Maeda T; Hidaka H; Aoki S; Yatsuki H; Okamoto N; Uemura T; Hatada I; Matsumoto N; Soejima H
FASEB J; 2020 Jan; 34(1):960-973. PubMed ID: 31914674
[TBL] [Abstract][Full Text] [Related]
6. The DNMT3A PWWP domain is essential for the normal DNA methylation landscape in mouse somatic cells and oocytes.
Kibe K; Shirane K; Ohishi H; Uemura S; Toh H; Sasaki H
PLoS Genet; 2021 May; 17(5):e1009570. PubMed ID: 34048432
[TBL] [Abstract][Full Text] [Related]
7. Two competing mechanisms of DNMT3A recruitment regulate the dynamics of de novo DNA methylation at PRC1-targeted CpG islands.
Weinberg DN; Rosenbaum P; Chen X; Barrows D; Horth C; Marunde MR; Popova IK; Gillespie ZB; Keogh MC; Lu C; Majewski J; Allis CD
Nat Genet; 2021 Jun; 53(6):794-800. PubMed ID: 33986537
[TBL] [Abstract][Full Text] [Related]
8. A DNMT3A PWWP mutation leads to methylation of bivalent chromatin and growth retardation in mice.
Sendžikaitė G; Hanna CW; Stewart-Morgan KR; Ivanova E; Kelsey G
Nat Commun; 2019 Apr; 10(1):1884. PubMed ID: 31015495
[TBL] [Abstract][Full Text] [Related]
9. NSD1 deposits histone H3 lysine 36 dimethylation to pattern non-CG DNA methylation in neurons.
Hamagami N; Wu DY; Clemens AW; Nettles SA; Gabel HW
bioRxiv; 2023 Feb; ():. PubMed ID: 36824816
[TBL] [Abstract][Full Text] [Related]
10. Genomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylation.
Baubec T; Colombo DF; Wirbelauer C; Schmidt J; Burger L; Krebs AR; Akalin A; Schübeler D
Nature; 2015 Apr; 520(7546):243-7. PubMed ID: 25607372
[TBL] [Abstract][Full Text] [Related]
11. Histone methylation mediated by NSD1 is required for the establishment and maintenance of neuronal identities.
Zheng Y; Zhao C; Song Q; Xu L; Zhang B; Hu G; Kong X; Li S; Li X; Shen Y; Zhuang L; Wu M; Liu Y; Zhou Y
Cell Rep; 2023 Dec; 42(12):113496. PubMed ID: 37995181
[TBL] [Abstract][Full Text] [Related]
12. Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging.
Jeffries AR; Maroofian R; Salter CG; Chioza BA; Cross HE; Patton MA; Dempster E; Temple IK; Mackay DJG; Rezwan FI; Aksglaede L; Baralle D; Dabir T; Hunter MF; Kamath A; Kumar A; Newbury-Ecob R; Selicorni A; Springer A; Van Maldergem L; Varghese V; Yachelevich N; Tatton-Brown K; Mill J; Crosby AH; Baple EL
Genome Res; 2019 Jul; 29(7):1057-1066. PubMed ID: 31160375
[TBL] [Abstract][Full Text] [Related]
13. The Dnmt3a PWWP domain reads histone 3 lysine 36 trimethylation and guides DNA methylation.
Dhayalan A; Rajavelu A; Rathert P; Tamas R; Jurkowska RZ; Ragozin S; Jeltsch A
J Biol Chem; 2010 Aug; 285(34):26114-20. PubMed ID: 20547484
[TBL] [Abstract][Full Text] [Related]
14. Correction to: DNMT3A reads and connects histone H3K36me2 to DNA methylation.
Xu W; Li J; Rong B; Zhao B; Wang M; Dai R; Chen Q; Liu H; Gu Z; Liu S; Guo R; Shen H; Wu F; Lan F
Protein Cell; 2020 Mar; 11(3):230. PubMed ID: 31814083
[TBL] [Abstract][Full Text] [Related]
15. Domain Structure of the Dnmt1, Dnmt3a, and Dnmt3b DNA Methyltransferases.
Tajima S; Suetake I; Takeshita K; Nakagawa A; Kimura H; Song J
Adv Exp Med Biol; 2022; 1389():45-68. PubMed ID: 36350506
[TBL] [Abstract][Full Text] [Related]
16. Structural basis for recognition of histone H3K36me3 nucleosome by human de novo DNA methyltransferases 3A and 3B.
Rondelet G; Dal Maso T; Willems L; Wouters J
J Struct Biol; 2016 Jun; 194(3):357-67. PubMed ID: 26993463
[TBL] [Abstract][Full Text] [Related]
17. Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions.
Heyn P; Logan CV; Fluteau A; Challis RC; Auchynnikava T; Martin CA; Marsh JA; Taglini F; Kilanowski F; Parry DA; Cormier-Daire V; Fong CT; Gibson K; Hwa V; Ibáñez L; Robertson SP; Sebastiani G; Rappsilber J; Allshire RC; Reijns MAM; Dauber A; Sproul D; Jackson AP
Nat Genet; 2019 Jan; 51(1):96-105. PubMed ID: 30478443
[TBL] [Abstract][Full Text] [Related]
18. H3K36 dimethylation shapes the epigenetic interaction landscape by directing repressive chromatin modifications in embryonic stem cells.
Chen H; Hu B; Horth C; Bareke E; Rosenbaum P; Kwon SY; Sirois J; Weinberg DN; Robison FM; Garcia BA; Lu C; Pastor WA; Majewski J
Genome Res; 2022 May; 32(5):825-837. PubMed ID: 35396277
[TBL] [Abstract][Full Text] [Related]
19. Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state.
Mauser R; Kungulovski G; Keup C; Reinhardt R; Jeltsch A
Epigenetics Chromatin; 2017 Sep; 10(1):45. PubMed ID: 28946896
[TBL] [Abstract][Full Text] [Related]
20. Co-occurrence of a maternally inherited
Polonis K; Blackburn PR; Urrutia RA; Lomberk GA; Kruisselbrink T; Cousin MA; Boczek NJ; Hoppman NL; Babovic-Vuksanovic D; Klee EW; Pichurin PN
Cold Spring Harb Mol Case Stud; 2018 Aug; 4(4):. PubMed ID: 29802153
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
