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MGI:Dnmt1

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Dnmt1 ( synonyms: Cxxc9, Dnmt1o, MommeD2, MTase )
Protein Name(s) DNA methyltransferase (cytosine-5) 1,
External Links
MGI MGI:94912

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0000792

heterochromatin

MGI:MGI:2682084
PMID:14519686[1]

IDA: Inferred from Direct Assay

C

From MGI

GO:0003677

DNA binding

MGI:MGI:2152690
PMID:11399088[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003677

DNA binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P26358

F

From MGI

GO:0003690

double-stranded DNA binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

F

From MGI

GO:0003723

RNA binding

MGI:MGI:4830046
PMID:20573698[3]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003824

catalytic activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0021

F

From MGI

GO:0003886

DNA (cytosine-5-)-methyltransferase activity

MGI:MGI:2152690
PMID:11399088[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0003886

DNA (cytosine-5-)-methyltransferase activity

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

F

From MGI

GO:0005515

protein binding

MGI:MGI:2448855
PMID:10888872[4]

IPI: Inferred from Physical Interaction

UniProtKB:P17918
UniProtKB:P70288
UniProtKB:Q9JI44

F

From MGI

GO:0005515

protein binding

MGI:MGI:3587127
PMID:16085498[5]

IPI: Inferred from Physical Interaction

UniProtKB:Q91YE5

F

From MGI

GO:0005515

protein binding

MGI:MGI:3687778
PMID:10615135[6]

IPI: Inferred from Physical Interaction

UniProtKB:O09106

F

From MGI

GO:0005515

protein binding

MGI:MGI:3778150
PMID:17931718[7]

IPI: Inferred from Physical Interaction

UniProtKB:Q61658

F

From MGI

GO:0005515

protein binding

MGI:MGI:4441123
PMID:15550930[8]

IPI: Inferred from Physical Interaction

UniProtKB:P12004

F

From MGI

GO:0005634

nucleus

MGI:MGI:2389598
PMID:11942627[9]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:3051927
PMID:15063176[10]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:3778150
PMID:17931718[7]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005634

nucleus

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

C

From MGI

GO:0005657

replication fork

MGI:MGI:2448855
PMID:10888872[4]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005721

centromeric heterochromatin

MGI:MGI:3852629
PMID:17576694[11]

IDA: Inferred from Direct Assay

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0963

C

From MGI

GO:0006306

DNA methylation

MGI:MGI:2152690
PMID:11399088[2]

IDA: Inferred from Direct Assay

P

From MGI

GO:0006351

transcription, DNA-dependent

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0804

P

From MGI

GO:0006355

regulation of transcription, DNA-dependent

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0805

P

From MGI

GO:0008134

transcription factor binding

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR010506

F

From MGI

GO:0008152

metabolic process

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0021

P

From MGI

GO:0008168

methyltransferase activity

MGI:MGI:3687778
PMID:10615135[6]

IDA: Inferred from Direct Assay

F

From MGI

GO:0008270

zinc ion binding

MGI:MGI:2152690
PMID:11399088[2]

IDA: Inferred from Direct Assay

F

From MGI

GO:0008327

methyl-CpG binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

F

From MGI

GO:0008327

methyl-CpG binding

MGI:MGI:4830046
PMID:20573698[3]

IDA: Inferred from Direct Assay

F

From MGI

GO:0009008

DNA-methyltransferase activity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P26358

F

From MGI

GO:0010216

maintenance of DNA methylation

MGI:MGI:3852629
PMID:17576694[11]

IMP: Inferred from Mutant Phenotype

P

From MGI

GO:0010216

maintenance of DNA methylation

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

P

From MGI

GO:0010216

maintenance of DNA methylation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P26358

P

From MGI

GO:0010424

DNA methylation on cytosine within a CG sequence

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

P

From MGI

GO:0010468

regulation of gene expression

MGI:MGI:3662835
PMID:16491076[12]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156895

P

From MGI

GO:0010628

positive regulation of gene expression

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P26358

P

From MGI

GO:0016458

gene silencing

MGI:MGI:3687778
PMID:10615135[6]

IDA: Inferred from Direct Assay

P

From MGI

GO:0016568

chromatin modification

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0156

P

From MGI

GO:0016740

transferase activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0808

F

From MGI

GO:0019904

protein domain specific binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

F

From MGI

GO:0032259

methylation

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0489

P

From MGI

GO:0042127

regulation of cell proliferation

MGI:MGI:1861347
PMID:10919675[13]

IGI: Inferred from Genetic Interaction

MGI:MGI:88039
MGI:MGI:104642

P

From MGI

GO:0042826

histone deacetylase binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

F

From MGI

GO:0043234

protein complex

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

C

From MGI

GO:0045322

unmethylated CpG binding

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

F

From MGI

GO:0045892

negative regulation of transcription, DNA-dependent

MGI:MGI:2448855
PMID:10888872[4]

IDA: Inferred from Direct Assay

P

From MGI

GO:0045892

negative regulation of transcription, DNA-dependent

MGI:MGI:3698916
PMID:17245608[14]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2156895

P

From MGI

GO:0046498

S-adenosylhomocysteine metabolic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

P

From MGI

GO:0046499

S-adenosylmethioninamine metabolic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

P

From MGI

GO:0046500

S-adenosylmethionine metabolic process

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

P

From MGI

GO:0046872

metal ion binding

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0479

F

From MGI

GO:0051571

positive regulation of histone H3-K4 methylation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P26358

P

From MGI

GO:0051573

negative regulation of histone H3-K9 methylation

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:P26358

P

From MGI

GO:0051718

DNA (cytosine-5-)-methyltransferase activity, acting on CpG substrates

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

F

From MGI

GO:0071230

cellular response to amino acid stimulus

MGI:MGI:4833768
PMID:20548288[15]

IDA: Inferred from Direct Assay

P

From MGI

GO:0090116

C-5 methylation of cytosine

MGI:MGI:4417868

ISO: Inferred from Sequence Orthology

NCBI:NP_445806

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. Craig JM et al. (2003) Analysis of mammalian proteins involved in chromatin modification reveals new metaphase centromeric proteins and distinct chromosomal distribution patterns. Hum Mol Genet 12: 3109-21 PubMed GONUTS page
  2. 2.0 2.1 2.2 2.3 Fatemi M et al. (2001) The activity of the murine DNA methyltransferase Dnmt1 is controlled by interaction of the catalytic domain with the N-terminal part of the enzyme leading to an allosteric activation of the enzyme after binding to methylated DNA. J Mol Biol 309: 1189-99 PubMed GONUTS page
  3. 3.0 3.1 Mohammad F et al. (2010) Kcnq1ot1 noncoding RNA mediates transcriptional gene silencing by interacting with Dnmt1. Development 137: 2493-9 PubMed GONUTS page
  4. 4.0 4.1 4.2 Rountree MR et al. (2000) DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at replication foci. Nat Genet 25: 269-77 PubMed GONUTS page
  5. Zhou Y & Grummt I (2005) The PHD finger/bromodomain of NoRC interacts with acetylated histone H4K16 and is sufficient for rDNA silencing. Curr Biol 15: 1434-8 PubMed GONUTS page
  6. 6.0 6.1 6.2 Fuks F et al. (2000) DNA methyltransferase Dnmt1 associates with histone deacetylase activity. Nat Genet 24: 88-91 PubMed GONUTS page
  7. 7.0 7.1 Sajedi E et al. (2008) DNMT1 interacts with the developmental transcriptional repressor HESX1. Biochim Biophys Acta 1783: 131-43 PubMed GONUTS page
  8. Easwaran HP et al. (2004) Replication-independent chromatin loading of Dnmt1 during G2 and M phases. EMBO Rep 5: 1181-6 PubMed GONUTS page
  9. Sakai Y et al. (2001) Expression of DNA methyltransferase (Dnmt1) in testicular germ cells during development of mouse embryo. Cell Struct Funct 26: 685-91 PubMed GONUTS page
  10. La Salle S et al. (2004) Windows for sex-specific methylation marked by DNA methyltransferase expression profiles in mouse germ cells. Dev Biol 268: 403-15 PubMed GONUTS page
  11. 11.0 11.1 Schermelleh L et al. (2007) Dynamics of Dnmt1 interaction with the replication machinery and its role in postreplicative maintenance of DNA methylation. Nucleic Acids Res 35: 4301-12 PubMed GONUTS page
  12. Bilic I et al. (2006) Negative regulation of CD8 expression via Cd8 enhancer-mediated recruitment of the zinc finger protein MAZR. Nat Immunol 7: 392-400 PubMed GONUTS page
  13. Cormier RT & Dove WF (2000) Dnmt1N/+ reduces the net growth rate and multiplicity of intestinal adenomas in C57BL/6-multiple intestinal neoplasia (Min)/+ mice independently of p53 but demonstrates strong synergy with the modifier of Min 1(AKR) resistance allele. Cancer Res 60: 3965-70 PubMed GONUTS page
  14. Green K et al. (2007) A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA. Mamm Genome 18: 32-42 PubMed GONUTS page
  15. Pogribny IP et al. (2010) Difference in expression of hepatic microRNAs miR-29c, miR-34a, miR-155, and miR-200b is associated with strain-specific susceptibility to dietary nonalcoholic steatohepatitis in mice. Lab Invest 90: 1437-46 PubMed GONUTS page
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