DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA Export

@article{citeulike:1544012, abstract = {Mammals use DNA methylation for the heritable silencing of retrotransposons and imprinted genes and for the inactivation of the X chromosome in females. The establishment of patterns of DNA methylation during gametogenesis depends in part on DNMT3L, an enzymatically inactive regulatory factor that is related in sequence to the DNA methyltransferases DNMT3A and DNMT3B1, 2. The main proteins that interact in vivo with the product of an epitope-tagged allele of the endogenous Dnmt3L gene were identified by mass spectrometry as DNMT3A2, DNMT3B and the four core histones. Peptide interaction assays showed that DNMT3L specifically interacts with the extreme amino terminus of histone H3; this interaction was strongly inhibited by methylation at lysine 4 of histone H3 but was insensitive to modifications at other positions. Crystallographic studies of human DNMT3L showed that the protein has a carboxy-terminal methyltransferase-like domain and an N-terminal cysteine-rich domain. Cocrystallization of DNMT3L with the tail of histone H3 revealed that the tail bound to the cysteine-rich domain of DNMT3L, and substitution of key residues in the binding site eliminated the H3 tail–DNMT3L interaction. These data indicate that DNMT3L recognizes histone H3 tails that are unmethylated at lysine 4 and induces de novo DNA methylation by recruitment or activation of DNMT3A2.}, author = {Ooi, Steen K. T. and Qiu, Chen and Bernstein, Emily and Li, Keqin and Jia, Da and Yang, Zhe and Erdjument-Bromage, Hediye and Tempst, Paul and Lin, Shau-Ping and Allis, C. David and Cheng, Xiaodong and Bestor, Timothy H.}, citeulike-article-id = {1544012}, citeulike-linkout-0 = {http://dx.doi.org/10.1038/nature05987}, citeulike-linkout-1 = {http://dx.doi.org/10.1038/nature05987}, citeulike-linkout-2 = {http://view.ncbi.nlm.nih.gov/pubmed/17687327}, citeulike-linkout-3 = {http://www.hubmed.org/display.cgi?uids=17687327}, day = {09}, doi = {10.1038/nature05987}, issn = {0028-0836}, journal = {Nature}, keywords = {dna-methylation, dnmt3l, histone}, month = {August}, number = {7154}, pages = {714--717}, posted-at = {2009-11-05 15:24:40}, priority = {2}, publisher = {Nature Publishing Group}, title = {DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA}, url = {http://dx.doi.org/10.1038/nature05987}, volume = {448}, year = {2007} }

TY - JOUR ID - citeulike:1544012 L3 - citeulike-article-id:1544012 N2 - Mammals use DNA methylation for the heritable silencing of retrotransposons and imprinted genes and for the inactivation of the X chromosome in females. The establishment of patterns of DNA methylation during gametogenesis depends in part on DNMT3L, an enzymatically inactive regulatory factor that is related in sequence to the DNA methyltransferases DNMT3A and DNMT3B1, 2. The main proteins that interact in vivo with the product of an epitope-tagged allele of the endogenous Dnmt3L gene were identified by mass spectrometry as DNMT3A2, DNMT3B and the four core histones. Peptide interaction assays showed that DNMT3L specifically interacts with the extreme amino terminus of histone H3; this interaction was strongly inhibited by methylation at lysine 4 of histone H3 but was insensitive to modifications at other positions. Crystallographic studies of human DNMT3L showed that the protein has a carboxy-terminal methyltransferase-like domain and an N-terminal cysteine-rich domain. Cocrystallization of DNMT3L with the tail of histone H3 revealed that the tail bound to the cysteine-rich domain of DNMT3L, and substitution of key residues in the binding site eliminated the H3 tail–DNMT3L interaction. These data indicate that DNMT3L recognizes histone H3 tails that are unmethylated at lysine 4 and induces de novo DNA methylation by recruitment or activation of DNMT3A2. IS - 7154 JF - Nature SN - 0028-0836 EP - 717 TI - DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA PB - Nature Publishing Group VL - 448 SP - 714 KW - dna-methylation KW - dnmt3l KW - histone AU - Ooi, Steen AU - Qiu, Chen AU - Bernstein, Emily AU - Li, Keqin AU - Jia, Da AU - Yang, Zhe AU - Erdjument-Bromage, Hediye AU - Tempst, Paul AU - Lin, Shau-Ping AU - Allis, David AU - Cheng, Xiaodong AU - Bestor, Timothy PY - 2007/08/09/ UR - http://dx.doi.org/10.1038/nature05987 ER -