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Items: 1 to 20 of 109

1.

Mouse oocyte methylomes at base resolution reveal genome-wide accumulation of non-CpG methylation and role of DNA methyltransferases.

Shirane K, Toh H, Kobayashi H, Miura F, Chiba H, Ito T, Kono T, Sasaki H.

PLoS Genet. 2013 Apr;9(4):e1003439. doi: 10.1371/journal.pgen.1003439.

2.

Contribution of intragenic DNA methylation in mouse gametic DNA methylomes to establish oocyte-specific heritable marks.

Kobayashi H, Sakurai T, Imai M, Takahashi N, Fukuda A, Yayoi O, Sato S, Nakabayashi K, Hata K, Sotomaru Y, Suzuki Y, Kono T.

PLoS Genet. 2012 Jan;8(1):e1002440. doi: 10.1371/journal.pgen.1002440.

3.

Coordinate regulation of DNA methyltransferase expression during oogenesis.

Lucifero D, La Salle S, Bourc'his D, Martel J, Bestor TH, Trasler JM.

BMC Dev Biol. 2007 Apr 19;7:36.

4.

Bovine DNA methylation imprints are established in an oocyte size-specific manner, which are coordinated with the expression of the DNMT3 family proteins.

O'Doherty AM, O'Shea LC, Fair T.

Biol Reprod. 2012 Mar 19;86(3):67. doi: 10.1095/biolreprod.111.094946.

PMID:
22088914
5.

Forced expression of DNA methyltransferases during oocyte growth accelerates the establishment of methylation imprints but not functional genomic imprinting.

Hara S, Takano T, Fujikawa T, Yamada M, Wakai T, Kono T, Obata Y.

Hum Mol Genet. 2014 Jul 15;23(14):3853-64. doi: 10.1093/hmg/ddu100.

6.

Dynamic expression of DNA methyltransferases (DNMTs) in oocytes and early embryos.

Uysal F, Akkoyunlu G, Ozturk S.

Biochimie. 2015 Sep;116:103-13. doi: 10.1016/j.biochi.2015.06.019. Review.

PMID:
26143007
7.

Distinct roles of DNMT1-dependent and DNMT1-independent methylation patterns in the genome of mouse embryonic stem cells.

Li Z, Dai H, Martos SN, Xu B, Gao Y, Li T, Zhu G, Schones DE, Wang Z.

Genome Biol. 2015 Jun 2;16:115. doi: 10.1186/s13059-015-0685-2.

8.

In vivo control of CpG and non-CpG DNA methylation by DNA methyltransferases.

Arand J, Spieler D, Karius T, Branco MR, Meilinger D, Meissner A, Jenuwein T, Xu G, Leonhardt H, Wolf V, Walter J.

PLoS Genet. 2012 Jun;8(6):e1002750. doi: 10.1371/journal.pgen.1002750.

9.

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 9;520(7546):243-7. doi: 10.1038/nature14176.

PMID:
25607372
10.

DNA methyltransferase loading, but not de novo methylation, is an oocyte-autonomous process stimulated by SCF signalling.

Lees-Murdock DJ, Lau HT, Castrillon DH, De Felici M, Walsh CP.

Dev Biol. 2008 Sep 1;321(1):238-50. doi: 10.1016/j.ydbio.2008.06.024.

11.

CpG sites preferentially methylated by Dnmt3a in vivo.

Oka M, Rodić N, Graddy J, Chang LJ, Terada N.

J Biol Chem. 2006 Apr 14;281(15):9901-8.

12.
13.

DNA methylation plays an important role in promoter choice and protein production at the mouse Dnmt3L locus.

O'Doherty AM, Rutledge CE, Sato S, Thakur A, Lees-Murdock DJ, Hata K, Walsh CP.

Dev Biol. 2011 Aug 15;356(2):411-20. doi: 10.1016/j.ydbio.2011.05.665.

14.

DNMT3L stimulates the DNA methylation activity of Dnmt3a and Dnmt3b through a direct interaction.

Suetake I, Shinozaki F, Miyagawa J, Takeshima H, Tajima S.

J Biol Chem. 2004 Jun 25;279(26):27816-23.

15.

De novo methylation of MMLV provirus in embryonic stem cells: CpG versus non-CpG methylation.

Dodge JE, Ramsahoye BH, Wo ZG, Okano M, Li E.

Gene. 2002 May 1;289(1-2):41-8.

PMID:
12036582
16.

DNMT3L modulates significant and distinct flanking sequence preference for DNA methylation by DNMT3A and DNMT3B in vivo.

Wienholz BL, Kareta MS, Moarefi AH, Gordon CA, Ginno PA, Chédin F.

PLoS Genet. 2010 Sep 9;6(9):e1001106. doi: 10.1371/journal.pgen.1001106.

17.

Cooperativity between DNA methyltransferases in the maintenance methylation of repetitive elements.

Liang G, Chan MF, Tomigahara Y, Tsai YC, Gonzales FA, Li E, Laird PW, Jones PA.

Mol Cell Biol. 2002 Jan;22(2):480-91.

18.

The DNA methyltransferase-like protein DNMT3L stimulates de novo methylation by Dnmt3a.

Chedin F, Lieber MR, Hsieh CL.

Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16916-21.

19.
20.

Genetic evidence for Dnmt3a-dependent imprinting during oocyte growth obtained by conditional knockout with Zp3-Cre and complete exclusion of Dnmt3b by chimera formation.

Kaneda M, Hirasawa R, Chiba H, Okano M, Li E, Sasaki H.

Genes Cells. 2010 Mar;15(3):169-79. doi: 10.1111/j.1365-2443.2009.01374.x.

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