KDM4C

Protein-coding gene in the species Homo sapiens
KDM4C
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2XDP, 2XML, 4XDO, 4XDP, 5FJK, 5FJH

Identifiers
AliasesKDM4C, GASC1, JHDM3C, JMJD2C, TDRD14C, bA146B14.1, lysine demethylase 4C
External IDsOMIM: 605469; MGI: 1924054; HomoloGene: 41004; GeneCards: KDM4C; OMA:KDM4C - orthologs
Gene location (Human)
Chromosome 9 (human)
Chr.Chromosome 9 (human)[1]
Chromosome 9 (human)
Genomic location for KDM4C
Genomic location for KDM4C
Band9p24.1Start6,720,863 bp[1]
End7,175,648 bp[1]
Gene location (Mouse)
Chromosome 4 (mouse)
Chr.Chromosome 4 (mouse)[2]
Chromosome 4 (mouse)
Genomic location for KDM4C
Genomic location for KDM4C
Band4|4 C3Start74,160,734 bp[2]
End74,324,097 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right hemisphere of cerebellum

  • epithelium of colon

  • bone marrow cells

  • tonsil

  • Achilles tendon

  • sural nerve

  • corpus callosum

  • body of pancreas

  • monocyte

  • granulocyte
Top expressed in
  • saccule

  • neural layer of retina

  • otic vesicle

  • otic placode

  • lacrimal gland

  • retinal pigment epithelium

  • granulocyte

  • interventricular septum

  • pineal gland

  • superior cervical ganglion
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
  • oxidoreductase activity
  • histone H3-methyl-lysine-9 demethylase activity
  • dioxygenase activity
  • metal ion binding
  • chromatin binding
  • enzyme binding
  • histone demethylase activity
  • androgen receptor binding
  • zinc ion binding
  • histone H3-methyl-lysine-36 demethylase activity
  • DNA-binding transcription repressor activity, RNA polymerase II-specific
  • methylated histone binding
Cellular component
  • nucleus
  • nucleoplasm
  • pericentric heterochromatin
  • histone methyltransferase complex
Biological process
  • regulation of transcription by RNA polymerase II
  • regulation of transcription, DNA-templated
  • transcription, DNA-templated
  • positive regulation of cell population proliferation
  • blastocyst formation
  • regulation of gene expression
  • positive regulation of gene expression
  • histone H3-K9 demethylation
  • positive regulation of neuron differentiation
  • negative regulation of histone H3-K9 trimethylation
  • regulation of stem cell population maintenance
  • regulation of stem cell differentiation
  • histone H3-K36 demethylation
  • chromatin organization
  • negative regulation of transcription by RNA polymerase II
  • chromatin remodeling
  • stem cell population maintenance
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

23081

76804

Ensembl

ENSG00000107077

ENSMUSG00000028397

UniProt

Q9H3R0

Q8VCD7

RefSeq (mRNA)
NM_001146694
NM_001146695
NM_001146696
NM_001304339
NM_001304340

NM_001304341
NM_015061
NM_001353997
NM_001353998
NM_001353999
NM_001354000
NM_001354001

NM_001172095
NM_144787
NM_001356561

RefSeq (protein)
NP_001140167
NP_001140168
NP_001291268
NP_001291269
NP_001291270

NP_055876
NP_001340926
NP_001340927
NP_001340928
NP_001340929
NP_001340930

NP_001165566
NP_659036
NP_001343490

Location (UCSC)Chr 9: 6.72 – 7.18 MbChr 4: 74.16 – 74.32 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Lysine-specific demethylase 4C is an enzyme that in humans is encoded by the KDM4C gene.[5][6][7]

Function

This gene is a member of the Jumonji domain 2 (JMJD2) family and encodes a protein with one JmjC domain, one JmjN domain, two PHD-type zinc fingers, and two Tudor domains. This nuclear protein belongs to the alpha-ketoglutarate-dependent hydroxylase superfamily. It functions as a trimethylation-specific demethylase, converting specific trimethylated histone residues to the dimethylated form. Chromosomal aberrations and increased transcriptional expression of this gene are associated with esophageal squamous cell carcinoma.[7] A expressional decrease of KDM4C was found during cardiac differentation of murine embryonic stem cells.[8]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000107077 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028397 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Nagase T, Ishikawa K, Suyama M, Kikuno R, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (Oct 1998). "Prediction of the coding sequences of unidentified human genes. XI. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 5 (5): 277–86. doi:10.1093/dnares/5.5.277. PMID 9872452.
  6. ^ Katoh M, Katoh M (Jun 2004). "Identification and characterization of JMJD2 family genes in silico". International Journal of Oncology. 24 (6): 1623–8. doi:10.3892/ijo.25.3.759. PMID 15138608.
  7. ^ a b "Entrez Gene: JMJD2C jumonji domain containing 2C".
  8. ^ Boeckel, Jes-Niels; Derlet, Anja; Glaser, Simone F.; Luczak, Annika; Lucas, Tina; Heumüller, Andreas W.; Krüger, Marcus; Zehendner, Christoph M.; Kaluza, David (July 2016). "JMJD8 Regulates Angiogenic Sprouting and Cellular Metabolism by Interacting With Pyruvate Kinase M2 in Endothelial Cells". Arteriosclerosis, Thrombosis, and Vascular Biology. 36 (7): 1425–1433. doi:10.1161/ATVBAHA.116.307695. ISSN 1524-4636. PMID 27199445.

Further reading

  • Yang ZQ, Imoto I, Fukuda Y, Pimkhaokham A, Shimada Y, Imamura M, Sugano S, Nakamura Y, Inazawa J (Sep 2000). "Identification of a novel gene, GASC1, within an amplicon at 9p23-24 frequently detected in esophageal cancer cell lines". Cancer Research. 60 (17): 4735–9. PMID 10987278.
  • Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, Ishii S, Sugiyama T, Saito K, Isono Y, Irie R, Kushida N, Yoneyama T, Otsuka R, Kanda K, Yokoi T, Kondo H, Wagatsuma M, Murakawa K, Ishida S, Ishibashi T, Takahashi-Fujii A, Tanase T, Nagai K, Kikuchi H, Nakai K, Isogai T, Sugano S (Jan 2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Research. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
  • Whetstine JR, Nottke A, Lan F, Huarte M, Smolikov S, Chen Z, Spooner E, Li E, Zhang G, Colaiacovo M, Shi Y (May 2006). "Reversal of histone lysine trimethylation by the JMJD2 family of histone demethylases". Cell. 125 (3): 467–81. doi:10.1016/j.cell.2006.03.028. PMID 16603238. S2CID 14461740.
  • Cloos PA, Christensen J, Agger K, Maiolica A, Rappsilber J, Antal T, Hansen KH, Helin K (Jul 2006). "The putative oncogene GASC1 demethylates tri- and dimethylated lysine 9 on histone H3". Nature. 442 (7100): 307–11. Bibcode:2006Natur.442..307C. doi:10.1038/nature04837. PMID 16732293. S2CID 2874903.
  • Wissmann M, Yin N, Müller JM, Greschik H, Fodor BD, Jenuwein T, Vogler C, Schneider R, Günther T, Buettner R, Metzger E, Schüle R (Mar 2007). "Cooperative demethylation by JMJD2C and LSD1 promotes androgen receptor-dependent gene expression". Nature Cell Biology. 9 (3): 347–53. doi:10.1038/ncb1546. PMID 17277772. S2CID 26006234.
  • Katoh Y, Katoh M (Aug 2007). "Comparative integromics on JMJD2A, JMJD2B and JMJD2C: preferential expression of JMJD2C in undifferentiated ES cells". International Journal of Molecular Medicine. 20 (2): 269–73. doi:10.3892/ijmm.20.2.269. PMID 17611647.
  • Zhao E, Ding J, Xia Y, Liu M, Ye B, Choi JH, Yan C, Dong Z, Huang S, Zha Y, Yang L, Cui H, Ding HF (2016). "KDM4C and ATF4 Cooperate in Transcriptional Control of Amino Acid Metabolism". Cell Reports. 14 (3): 506–519. doi:10.1016/j.celrep.2015.12.053. PMC 4731315. PMID 26774480.
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1.14.11: 2-oxoglutarate1.14.13: NADH or NADPH1.14.14: reduced flavin or flavoprotein1.14.15: reduced iron–sulfur protein1.14.16: reduced pteridine (BH4 dependent)1.14.17: reduced ascorbate1.14.18-19: other1.14.99 - miscellaneous
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