HCSGD entry for DNMT3A
1. General information
Official gene symbol | DNMT3A |
---|---|
Entrez ID | 1788 |
Gene full name | DNA (cytosine-5-)-methyltransferase 3 alpha |
Other gene symbols | DNMT3A2 M.HsaIIIA |
Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network

3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
---|---|---|---|
GO:0000122 | Negative regulation of transcription from RNA polymerase II promoter | IEA | biological_process |
GO:0000775 | Chromosome, centromeric region | IEA | cellular_component |
GO:0000791 | Euchromatin | IDA | cellular_component |
GO:0003677 | DNA binding | IDA IEA | molecular_function |
GO:0003682 | Chromatin binding | IEA | molecular_function |
GO:0003886 | DNA (cytosine-5-)-methyltransferase activity | IDA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005634 | Nucleus | IDA | cellular_component |
GO:0005720 | Nuclear heterochromatin | IEA | cellular_component |
GO:0005730 | Nucleolus | IDA | cellular_component |
GO:0005737 | Cytoplasm | IDA | cellular_component |
GO:0006306 | DNA methylation | IDA IEA | biological_process |
GO:0006346 | Methylation-dependent chromatin silencing | IEA | biological_process |
GO:0006349 | Regulation of gene expression by genetic imprinting | TAS | biological_process |
GO:0007283 | Spermatogenesis | IEA | biological_process |
GO:0008168 | Methyltransferase activity | IEA | molecular_function |
GO:0010424 | DNA methylation on cytosine within a CG sequence | IEA | biological_process |
GO:0016363 | Nuclear matrix | IDA | cellular_component |
GO:0043045 | DNA methylation involved in embryo development | IEA | biological_process |
GO:0043046 | DNA methylation involved in gamete generation | IEA | biological_process |
GO:0044027 | Hypermethylation of CpG island | IEA | biological_process |
GO:0045322 | Unmethylated CpG binding | IEA | molecular_function |
GO:0046498 | S-adenosylhomocysteine metabolic process | IEA | biological_process |
GO:0046499 | S-adenosylmethioninamine metabolic process | IEA | biological_process |
GO:0046872 | Metal ion binding | IEA | molecular_function |
GO:0051718 | DNA (cytosine-5-)-methyltransferase activity, acting on CpG substrates | IEA | molecular_function |
GO:0071230 | Cellular response to amino acid stimulus | IEA | biological_process |
GO:0090116 | C-5 methylation of cytosine | IDA | biological_process |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.2773475362 | 0.3369027735 | 0.9742512345 | 1.0000000000 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
Data source | Up or down | Log fold change |
---|---|---|
GSE11954 | Down | -0.0035356576 |
GSE13712_SHEAR | Down | -0.2709296506 |
GSE13712_STATIC | Down | -0.0309953724 |
GSE19018 | Down | -0.2963234888 |
GSE19899_A1 | Up | 0.0434329011 |
GSE19899_A2 | Up | 0.5489789639 |
PubMed_21979375_A1 | Up | 0.5657113119 |
PubMed_21979375_A2 | Up | 0.5404052867 |
GSE35957 | Down | -0.4599700138 |
GSE36640 | Down | -1.7072559454 |
GSE54402 | Down | -0.2529815282 |
GSE9593 | Down | -0.3423569717 |
GSE43922 | Up | 0.0572972484 |
GSE24585 | Down | -0.1550689003 |
GSE37065 | Down | -0.1246759943 |
GSE28863_A1 | Up | 0.1897211389 |
GSE28863_A2 | Up | 0.5534801379 |
GSE28863_A3 | Down | -0.0262053303 |
GSE28863_A4 | Up | 0.4275894969 |
GSE48662 | Up | 0.2319515118 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Not regulated by drugs
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-143-3p | MIMAT0000435 | MIRT000716 | qRT-PCR//Luciferase reporter assay//Western blot | Functional MTI | 19638978 |
hsa-miR-29a-3p | MIMAT0000086 | MIRT003021 | Luciferase reporter assay//Western blot//qRT-PCR//Reporter assay;Other | Functional MTI | 17890317 |
hsa-miR-29a-3p | MIMAT0000086 | MIRT003021 | Immunohistochemistry//Microarray//Western blot | Functional MTI | 20643754 |
hsa-miR-29c-3p | MIMAT0000681 | MIRT003028 | Luciferase reporter assay//Western blot//qRT-PCR//Reporter assay;Other | Functional MTI | 17890317 |
hsa-miR-29c-3p | MIMAT0000681 | MIRT003028 | Immunohistochemistry//Microarray//Western blot | Functional MTI | 20643754 |
hsa-miR-29c-3p | MIMAT0000681 | MIRT003028 | Luciferase reporter assay//Western blot | Functional MTI | 23516428 |
hsa-miR-29b-3p | MIMAT0000100 | MIRT003029 | Luciferase reporter assay//Western blot//qRT-PCR//Reporter assay;Other | Functional MTI | 17890317 |
hsa-miR-29b-3p | MIMAT0000100 | MIRT003029 | Luciferase reporter assay | Functional MTI | 19211935 |
hsa-miR-29b-3p | MIMAT0000100 | MIRT003029 | Immunohistochemistry//Microarray//Western blot | Functional MTI | 20643754 |
hsa-miR-194-5p | MIMAT0000460 | MIRT005897 | Luciferase reporter assay//qRT-PCR//Western blot | Functional MTI | 20979124 |
hsa-miR-369-5p | MIMAT0001621 | MIRT005960 | Luciferase reporter assay//Reporter assay | Functional MTI | 21136442 |
hsa-miR-101-3p | MIMAT0000099 | MIRT007188 | Immunohistochemistry//Luciferase reporter assay//qRT-PCR//Western blot | Functional MTI | 23124077 |
hsa-miR-193b-3p | MIMAT0002819 | MIRT016379 | Microarray | Functional MTI (Weak) | 20304954 |
hsa-miR-18a-3p | MIMAT0002891 | MIRT040898 | CLASH | Functional MTI (Weak) | 23622248 |
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- mirRecord
MicroRNA name | mirBase ID | Target site number | MiRNA mature ID | Test method inter | MiRNA regulation site | Reporter target site | Pubmed ID |
---|---|---|---|---|---|---|---|
hsa-miR-29a-3p | MIMAT0000086 | 1 | hsa-miR-29a | 17890317 | |||
hsa-miR-29b-3p | MIMAT0000100 | 1 | hsa-miR-29b | 17890317 | |||
hsa-miR-29c-3p | MIMAT0000681 | 1 | hsa-miR-29c | 17890317 | |||
hsa-miR-29b-3p | MIMAT0000100 | 1 | hsa-miR-29b | {Western blot} | {overexpression by miRNA precursor transfection} | 19211935 | |
hsa-miR-143-3p | MIMAT0000435 | 1 | hsa-miR-143 | {Western blot} | {endogenous} | 19638978 |
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6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
27147278 | Prominent examples include aberrations in cytokines and their signaling pathways (such as tumor necrosis factor-alpha, interferon-gamma, SMAD proteins), mutations in genes encoding the RNA splicing machinery (SF3B1, SRSF2, ZRSR2, and U2AF1 genes), mutations in genes disrupting the epigenetic machinery (TET2, DNMT3A, DNMT3B, EZH2, ASXL1) |
21660946 | Expression of the de novo DNA methyltransferases DNMT3A and DNMT3B was up-regulated by transfection of miR-371 whereas expression of DNMT3A was down-regulated by miR-369-5p |
20473858 | DNMT3a plays a role in switches between doxorubicin-induced senescence and apoptosis of colorectal cancer cells |
20473858 | Here, we report that the DNA methyltransferase (DNMT) DNMT3a was upregulated by Dox especially at concentrations that induced apoptosis in HCT116 colorectal cancer cells, and this process was regulated by p53 |
20473858 | The differential expression of DNMT3a and p21 in response to Dox suggests that DNMT3a may be a key factor in switches between Dox-induced senescence and apoptosis |
20473858 | Moreover, when DNMT3a was silenced, treatment of HCT116 cells with apoptosis-inducing concentration of Dox increased the percentage of cells undergoing senescence, accompanied by upregulation of p21 |
20473858 | Surprisingly, no changes in DNA methylation status at p21 promoter were detected at either ranges of Dox, although DNMT3a and HDAC1 were recruited to p21 promoter at apoptosis-inducing Dox concentration, where they were present in the same complex |
20473858 | Overall, these data demonstrate that DNMT3a impacts the expression of p21 and plays a role in determining the Dox-induced senescence and apoptosis in HCT116 cells |
18723031 | The levels of DNMT3b and methyl-CpG binding protein 2 (MeCP2) increased in both mid-aged and replicative senescent cells, while DNMT3a and MBD2 were upregulated in the mid-aged cells |
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