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Relevant bibliographies by topics / DNMT2

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Academic literature on the topic 'DNMT2'

Author: Grafiati

Published: 10 December 2022

Last updated: 31 July 2025

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Journal articles on the topic "DNMT2"

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MUND, Cora, Tanja MUSCH, Martin STRÖDICKE, Birte ASSMANN, En LI, and Frank LYKO. "Comparative analysis of DNA methylation patterns in transgenic Drosophila overexpressing mouse DNA methyltransferases." Biochemical Journal 378, no. 3 (2004): 763–68. http://dx.doi.org/10.1042/bj20031567.

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DNA methyltransferases (Dnmts) mediate the epigenetic modification of eukaryotic genomes. Mammalian DNA methylation patterns are established and maintained by co-operative interactions among the Dnmt proteins Dnmt1, Dnmt3a and Dnmt3b. Owing to their simultaneous presence in mammalian cells, the activities of individual Dnmt have not yet been determined. This includes a fourth putative Dnmt, namely Dnmt2, which has failed to reveal any activity in previous assays. We have now established transgenic Drosophila strains that allow for individual overexpression of all known mouse Dnmts. Quantitativ

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Liu, Kui, Yun Fei Wang, Carmen Cantemir, and Mark T. Muller. "Endogenous Assays of DNA Methyltransferases: Evidence for Differential Activities of DNMT1, DNMT2, and DNMT3 in Mammalian Cells In Vivo." Molecular and Cellular Biology 23, no. 8 (2003): 2709–19. http://dx.doi.org/10.1128/mcb.23.8.2709-2719.2003.

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ABSTRACT While CpG methylation can be readily analyzed at the DNA sequence level in wild-type and mutant cells, the actual DNA (cytosine-5) methyltransferases (DNMTs) responsible for in vivo methylation on genomic DNA are less tractable. We used an antibody-based method to identify specific endogenous DNMTs (DNMT1, DNMT1b, DNMT2, DNMT3a, and DNMT3b) that stably and selectively bind to genomic DNA containing 5-aza-2′-deoxycytidine (aza-dC) in vivo. Selective binding to aza-dC-containing DNA suggests that the engaged DNMT is catalytically active in the cell. DNMT1b is a splice variant of the pre

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Del Castillo Falconi, Victor M., Karla Torres-Arciga, Genaro Matus-Ortega, José Díaz-Chávez, and Luis A. Herrera. "DNA Methyltransferases: From Evolution to Clinical Applications." International Journal of Molecular Sciences 23, no. 16 (2022): 8994. http://dx.doi.org/10.3390/ijms23168994.

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DNA methylation is an epigenetic mark that living beings have used in different environments. The MTases family catalyzes DNA methylation. This process is conserved from archaea to eukaryotes, from fertilization to every stage of development, and from the early stages of cancer to metastasis. The family of DNMTs has been classified into DNMT1, DNMT2, and DNMT3. Each DNMT has been duplicated or deleted, having consequences on DNMT structure and cellular function, resulting in a conserved evolutionary reaction of DNA methylation. DNMTs are conserved in the five kingdoms of life: bacteria, protis

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Papakonstantinou, Efthymia, Ioanna Pappa, Georgios Androutsopoulos, Georgios Adonakis, Ioannis Maroulis, and Vasiliki Tzelepi. "Comprehensive Analysis of DNA Methyltransferases Expression in Primary and Relapsed Ovarian Carcinoma." Cancers 15, no. 20 (2023): 4950. http://dx.doi.org/10.3390/cancers15204950.

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Background: Despite recent advances in epithelial ovarian carcinoma (EOC) treatment, its recurrence and mortality rates have not improved significantly. DNA hypermethylation has generally been associated with an ominous prognosis and chemotherapy resistance, but the role of DNA methyltransferases (DNMTs) in EOC remains to be investigated. Methods: In the current study, we systematically retrieved gene expression data from patients with EOC and studied the immunohistochemical expression of DNMTs in 108 primary and 26 relapsed tumors. Results: Our results showed that the DNMT1, DNMT3A, DNMT3B an

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KIM, SEON-HEE, HYE-JEONG CHO, WOON-MOK SOHN, et al. "Egg-specific expression of protein with DNA methyltransferase activity in the biocarcinogenic liver fluke Clonorchis sinensis." Parasitology 142, no. 9 (2015): 1228–38. http://dx.doi.org/10.1017/s0031182015000566.

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SUMMARYDespite recent reports regarding the biology of cytosine methylation in Schistosoma mansoni, the impact of the regulatory machinery remains unclear in diverse platyhelminthes. This ambiguity is reinforced by discoveries of DNA methyltransferase 2 (DNMT2)-only organisms and the substrate specificity of DNMT2 preferential to RNA molecules. Here, we characterized a novel DNA methyltransferase, named CsDNMT2, in a liver fluke Clonorchis sinensis. The protein exhibited structural properties conserved in other members of the DNMT2 family. The native and recombinant CsDNMT2 exhibited considera

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Zhu, Huolan, Xiang Wang, Xuyang Meng, et al. "Selenium Supplementation Improved Cardiac Functions by Suppressing DNMT2-Mediated GPX1 Promoter DNA Methylation in AGE-Induced Heart Failure." Oxidative Medicine and Cellular Longevity 2022 (April 6, 2022): 1–12. http://dx.doi.org/10.1155/2022/5402997.

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Objective. Advanced glycation end products (AGEs) are featured metabolites associated with diabetic cardiomyopathy which is characterized by heart failure caused by myocyte apoptosis. Selenium was proved cardioprotective. This study was aimed at investigating the therapeutic effects and underlying mechanisms of selenium supplementation on AGE-induced heart failure. Methods. Rats and primary myocytes were exposed to AGEs. Selenium supplementation was administrated. Cardiac functions and myocyte apoptosis were evaluated. Oxidative stress was assessed by total antioxidant capacity (TAC), reactive

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Huang, Zhi-Xuan, Jing Li, Qing-Ping Xiong, Hao Li, En-Duo Wang, and Ru-Juan Liu. "Position 34 of tRNA is a discriminative element for m5C38 modification by human DNMT2." Nucleic Acids Research 49, no. 22 (2021): 13045–61. http://dx.doi.org/10.1093/nar/gkab1148.

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Abstract Dnmt2, a member of the DNA methyltransferase superfamily, catalyzes the formation of 5-methylcytosine at position 38 in the anticodon loop of tRNAs. Dnmt2 regulates many cellular biological processes, especially the production of tRNA-derived fragments and intergenerational transmission of paternal metabolic disorders to offspring. Moreover, Dnmt2 is closely related to human cancers. The tRNA substrates of mammalian Dnmt2s are mainly detected using bisulfite sequencing; however, we lack supporting biochemical data concerning their substrate specificity or recognition mechanism. Here,

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Vivekanandan, Perumal, Hubert Darius-J. Daniel, Rajesh Kannangai, Francisco Martinez-Murillo, and Michael Torbenson. "Hepatitis B Virus Replication Induces Methylation of both Host and Viral DNA." Journal of Virology 84, no. 9 (2010): 4321–29. http://dx.doi.org/10.1128/jvi.02280-09.

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ABSTRACT Control of viral replication is a major therapeutic goal to reduce morbidity and mortality from chronic hepatitis B virus (HBV) infection. Recently, methylation has been identified as a novel host defense mechanism, and methylation of viral DNA leads to downregulation of HBV gene expression. To better understand the mechanisms of HBV methylation, cell lines were exposed to HBV using a model system that mimics natural infection and the expression of host DNA methyltransferase genes (DNMTs) was measured. DNMT1, DNMT2, and DNMT3 were all significantly upregulated in response to HBV. DNMT

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Lyko, Frank. "RNA Methylation and Its Role in the Hematopoietic System." Blood 130, Suppl_1 (2017): SCI—52—SCI—52. http://dx.doi.org/10.1182/blood.v130.suppl_1.sci-52.sci-52.

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Abstract RNA methylation represents a novel expansion of traditional epigenetic concepts. RNAs can be methylated at adenine and at cytosine residues, and both modifications have distinct regulatory potential. Our work focuses on the DNMT2 enzyme, which is a member of the animal (cytosine-5) DNA methyltransferase family and has long been considered to function as a DNA methyltransferase. However, a DNA methyltransferase activity could not be confirmed conclusively and more recent work clearly demonstrates that DNMT2 is a tRNA methyltransferase. This unexpected substrate is interpreted to reflec

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Goll, Mary Grace, Finn Kirpekar, Keith A. Maggert, et al. "Methylation of tRNAAsp by the DNA Methyltransferase Homolog Dnmt2." Science 311, no. 5759 (2006): 395–98. http://dx.doi.org/10.1126/science.1120976.

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The sequence and the structure of DNA methyltransferase-2 (Dnmt2) bear close affinities to authentic DNA cytosine methyltransferases. A combined genetic and biochemical approach revealed that human DNMT2 did not methylate DNA but instead methylated a small RNA; mass spectrometry showed that this RNA is aspartic acid transfer RNA (tRNAAsp) and that DNMT2 specifically methylated cytosine 38 in the anticodon loop. The function of DNMT2 is highly conserved, and human DNMT2 protein restored methylation in vitro to tRNAAsp from Dnmt2-deficient strains of mouse, Arabidopsis thaliana, and Drosophila m

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Dissertations / Theses on the topic "DNMT2"

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Müller, Sara [Verfasser]. "Biologische Funktionsanalyse und Identifizierung neuer Substrate der Methyltransferase Dnmt2 / Sara Müller." Kassel : Universitätsbibliothek Kassel, 2012. http://d-nb.info/101926845X/34.

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Kiani, Jafar. "Hérédité épigénétique et méthylation des ARNs : rôle de la méthyltransférase Dnmt2." Nice, 2011. http://www.theses.fr/2011NICE4093.

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Epigenetics deals with heritable alterations in gene expression that is not based on changes n DNA sequence. It was thought that DNA methylation and chromatin-encoded epigenetic information were the only epigenetic marks transmitted to the following generations. Recently, our group described the role of RNA in hereditary epigenetic variation, paramutation in mice. The role of RNA was demonstrated by the establishment of a heritable phenotype following microinjection into one-cell embryos of Kit heterozygous sperm RNA. It was further confirmed by induction of hereditary phenotypes after microin

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Schuster, Isabelle [Verfasser]. "Strukturelle und funktionelle Charakterisierung des Dnmt2-Homologs DnmA von Dictyostelium discoideum / Isabelle Schuster." Kassel : Universitätsbibliothek Kassel, 2016. http://d-nb.info/1101616091/34.

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Hartmann, Mark [Verfasser], and Frank [Akademischer Betreuer] Lyko. "Centromeric tRNA and Dnmt2-mediated Methylation in Mitotic Chromosome Segregation / Mark Hartmann ; Betreuer: Frank Lyko." Heidelberg : Universitätsbibliothek Heidelberg, 2018. http://d-nb.info/1177148862/34.

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Durdevic, Zeljko [Verfasser], and Frank [Akademischer Betreuer] Lyko. "Characterization of the Biological Function of Dnmt2 in Drosophila melanogaster / Zeljko Durdevic ; Betreuer: Frank Lyko." Heidelberg : Universitätsbibliothek Heidelberg, 2013. http://d-nb.info/1177249774/34.

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Kaiser, Steffen [Verfasser]. "Investigations on DNA methylation by Dnmt2 and impact of tRNA modifications on TLR7 stimulation / Steffen Kaiser." Mainz : Universitätsbibliothek Mainz, 2015. http://d-nb.info/1080401431/34.

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Shanmugam, Raghuvaran [Verfasser], and Albert [Akademischer Betreuer] Jeltsch. "Biochemical characterisation of tRNA-Asp methyltransferase Dnmt2 and its physiological significance / Raghuvaran Shanmugam. Betreuer: Albert Jeltsch." Stuttgart : Universitätsbibliothek der Universität Stuttgart, 2014. http://d-nb.info/1049931661/34.

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Vieira, Gilberto Cavalheiro. "Modelagem molecular e imunodetecção de DNA Metiltransferases 2 de Drosofilídeos : uma abordagem evolutiva da enigmática DNMT2." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2015. http://hdl.handle.net/10183/117889.

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A metilação do DNA genômico é um dos principais mecanismos de regulação epigenética nos organismos. Dentre as diferentes classes de DNA MTase, as m5C-MTase são as que se distribuem amplamente de procariotos a eucariotos. Em vertebrados existem três diferentes famílias: DNMT1, DNMT2 e DNMT3a e 3b. A DNMT1 possui atividade junto ao DNA hemimetilado. As DNMT3a e 3b são responsáveis pela metilação de novo. Já a subfamília DNMT2 possui seus sítios catalíticos altamente conservados, desde procariotos até eucariotos, possuindo propriedades que permitem executar funções tanto de metilação de novo, ass

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Liebers, Reinhard Kai [Verfasser], and Frank [Akademischer Betreuer] Lyko. "Dnmt2 in RNA methylation, RNA inheritance, and environmental responses in the mouse / Reinhard Kai Liebers ; Betreuer: Frank Lyko." Heidelberg : Universitätsbibliothek Heidelberg, 2016. http://d-nb.info/1180614186/34.

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Liebers, Reinhard [Verfasser], and Frank [Akademischer Betreuer] Lyko. "Dnmt2 in RNA methylation, RNA inheritance, and environmental responses in the mouse / Reinhard Kai Liebers ; Betreuer: Frank Lyko." Heidelberg : Universitätsbibliothek Heidelberg, 2016. http://d-nb.info/1180614186/34.

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Book chapters on the topic "DNMT2"

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Arnemann, J. "DNA-Methyltransferase (DNMT)." In Springer Reference Medizin. Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_3463.

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Arnemann, J. "DNA-Methyltransferase (DNMT)." In Lexikon der Medizinischen Laboratoriumsdiagnostik. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-49054-9_3463-1.

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Yildiz, Can Bora, and Geraldine Zimmer-Bensch. "Role of DNMTs in the Brain." In Advances in Experimental Medicine and Biology. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-11454-0_15.

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Tajima, Shoji, Isao Suetake, Kohei Takeshita, Atsushi Nakagawa, and Hironobu Kimura. "Domain Structure of the Dnmt1, Dnmt3a, and Dnmt3b DNA Methyltransferases." In Advances in Experimental Medicine and Biology. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-43624-1_4.

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Tajima, Shoji, Isao Suetake, Kohei Takeshita, Atsushi Nakagawa, Hironobu Kimura, and Jikui Song. "Domain Structure of the Dnmt1, Dnmt3a, and Dnmt3b DNA Methyltransferases." In Advances in Experimental Medicine and Biology. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-11454-0_3.

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Amruth Maroju, Pranay, and Kommu Naga Mohan. "DNA Methyltransferases and Schizophrenia: Current Status." In Psychosis - Phenomenology, Psychopathology and Pathophysiology [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.98567.

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Schizophrenia (SZ) is a complex disorder without a single cause but with multiple etiologies. Monozygotic twin studies suggesting high discordant rates provide evidence for epigenetic mechanisms among the factors that result in increased susceptibility. Among the different epigenetic modifications in mammals, DNA methylation mediated by DNA methyltransferases (DNMTs) is the most-well studied. Studies on post-mortem brain samples and blood samples of SZ patients revealed altered levels of most DNMTs. In addition, some recent studies also reported disease-associated SNPs in the DNMT genes. While

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Svedružić, Željko M. "Dnmt1." In Progress in Molecular Biology and Translational Science. Elsevier, 2011. http://dx.doi.org/10.1016/b978-0-12-387685-0.00006-8.

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"DNMTs." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-16483-5_1698.

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"Methyltransferase, DNA (dnmt1, dnmt1-b, 19p13.3-p13.2)." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_10292.

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Sharif, Jafar, and Haruhiko Koseki. "Recruitment of Dnmt1." In Progress in Molecular Biology and Translational Science. Elsevier, 2011. http://dx.doi.org/10.1016/b978-0-12-387685-0.00008-1.

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Conference papers on the topic "DNMT2"

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Laranjeira, Angelo B., Erich Huang, Larry Rubinstein, Dat Nguyen, and Sherry X. Yang. "Abstract 3847: Knockout of DNMT1 using CRISPR gene-editing technology confers resistance to DNMT inhibitors in human breast cancer cells." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-3847.

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Laranjeira, Angelo B., Erich Huang, Larry Rubinstein, Dat Nguyen, and Sherry X. Yang. "Abstract 3847: Knockout of DNMT1 using CRISPR gene-editing technology confers resistance to DNMT inhibitors in human breast cancer cells." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-3847.

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Cai, Yi, Hsing-chen Tsai, Ray-whay Yen, Limin Xia, Yang Zhang, and Stephen Baylin. "Abstract LB-150: Genetic depletion of DNMT1 reveals a DNMT1 threshold controlling DNA methylation in human cells." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-lb-150.

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Laranjeira, Angelo B., Dat Nguyen, Erich Huang, James H. Doroshow, and Sherry X. Yang. "Abstract 5081: Disruption of DNA methyltransferase (DNMT) 1 confers resistance to DNMT inhibitors in human colorectal cancer cells." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-5081.

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Ferreira, Nancy, Darley Ferreira, and Thais Ferreira. "GENETIC EVALUATION OF MICROCALCIFICATIONS AS A PROGNOSTIC FACTOR." In Abstracts from the Brazilian Breast Cancer Symposium - BBCS 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s2101.

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Introduction: Breast cancer is the most recurring type of cancer among women, with reduced mortality at an initial stage of lesion. From a radiological perspective, perceived microcalcifications may be associated with histological findings such as proliferative injuries with or without atypical features and ductal carcinoma in situ. Currently, percutaneous and vacuum biopsies allow for the correlation between anatomoradiological and identification of previous lesions and those that offer the risk of cancer. No biomarker has been established to predict the risk of cancer in women diagnosed with

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SILVA, CAMILA T. DA, Fernanda Molognoni, Fabiana H. M. de Melo, and Miriam Galvonas Jasiulionis. "Abstract 426: Transcriptional regulation of dnmt1 by E2F1 in melanoma progression." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-426.

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Lee, Gun Eui, and Keith D. Robertson. "Abstract 1054: The role of DNMT1 in the DNA damage response." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-1054.

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Martínez Fernández, Liliam, and Jose Luis Medina Franco. "Identification of novel DNA Methyltransferase 1 (DNMT1) inhibitors from focused databases." In 7th International Electronic Conference on Medicinal Chemistry. MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11570.

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Saif, Haddad, Skorupinska Mariola, Rossor Alex, et al. "A unique patient with DNM2 related peripheral neuropathy with myopathy." In Association of British Neurologists: Annual Meeting Abstracts 2023. BMJ Publishing Group Ltd, 2023. http://dx.doi.org/10.1136/jnnp-2023-abn.272.

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Tohme, Rita, Francis Enane, Caroline Schuerger, et al. "Abstract 1088: Advancing non-cytotoxic DNMT1-targeting to treat chemorefractory pancreatic cancer." In Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-1088.

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Reports on the topic "DNMT2"

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Sarkisova, Karine, A. Gabova, E. Fedosova, et al. Maternal methyl-enriched diet reduces absence seizures and depression-like comorbidity, and increases DNMT1 and HCN1 gene expression in the somatosensory cortex in adult offspring. LLC MAKS Press, 2020. http://dx.doi.org/10.29003/m1395.fens-2020.

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