JARID1B

Last updated
KDM5B
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases KDM5B , CT31, JARID1B, PLU-1, PLU1, PPP1R98, PUT1, RBBP2H1A, RBP2-H1, lysine demethylase 5B, MRT65
External IDs OMIM: 605393 MGI: 1922855 HomoloGene: 48448 GeneCards: KDM5B
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001314042
NM_006618
NM_001347591
NM_001399817

NM_152895

RefSeq (protein)

NP_001300971
NP_001334520
NP_006609

NP_690855

Location (UCSC) Chr 1: 202.72 – 202.81 Mb Chr 1: 134.49 – 134.56 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Lysine-specific demethylase 5B also known as histone demethylase JARID1B is a demethylase enzyme that in humans is encoded by the KDM5B gene. [5] [6] [7] JARID1B belongs to the alpha-ketoglutarate-dependent hydroxylase superfamily.

Function

Jarid1B (also known as KDM5B or PLU1) is in the family of JHDM genes. These are responsible for demethylation of tri- and di-methylated lysines in the 4 position of histone 3 (H3K4me3 and H3K4me2). Jarid1B is a multidomain enzyme that is part of the subfamily KDM5. The whole Jarid1 family is a protein family that possesses H3K4 histone demethylase activity. [8]

Jarid1B has been implicated in the development of prostate, breast, and skin cancer and also has been associated with melanoma maintenance. Knockout mice (Jarid1b−/−) produced are viable in neonatal life. These mice do exhibit the phenotype of premature mortality, decreased fertility in female mice, reduction in body weight and impairment in mammary gland development. It also acted to decrease serum estrogen levels and caused reduced mammary epithelial cell proliferation in the early stages of puberty. These Jarid1b−/− mice seem to be greatly affected in many regulators of the development of mammy development such as FOXA1 and estrogen receptor α. [9] However, others have shown that a Jarid1B knockout embryos usually have neonatal lethality due to the failure of their respiratory system. Knockout embryos have also been seen to have several different neural defects including: disorganized cranial nerves, increased incidences of exencephaly, and defects in eye development. [10]

Interactions

JARID1B has been shown to interact with FOXG1 [11] and PAX9. [11]

Related Research Articles

<span class="mw-page-title-main">KDM1A</span> Protein-coding gene in the species Homo sapiens

Lysine-specific histone demethylase 1A (LSD1) also known as lysine (K)-specific demethylase 1A (KDM1A) is a protein that in humans is encoded by the KDM1A gene. LSD1 is a flavin-dependent monoamine oxidase, which can demethylate mono- and di-methylated lysines, specifically histone 3, lysine 4 (H3K4). Other reported methylated lysine substrates such as histone H3K9 and TP53 have not been biochemically validated. This enzyme plays a critical role in oocyte growth, embryogenesis, hematopoiesis and tissue-specific differentiation. LSD1 was the first histone demethylase to be discovered though more than 30 have since been described.

<span class="mw-page-title-main">TP53BP1</span> Protein-coding gene in the species Homo sapiens

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<span class="mw-page-title-main">Methyl-CpG-binding domain protein 2</span> Protein-coding gene in the species Homo sapiens

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<span class="mw-page-title-main">MTA1</span> Protein-coding gene in the species Homo sapiens

Metastasis-associated protein MTA1 is a protein that in humans is encoded by the MTA1 gene. MTA1 is the founding member of the MTA family of genes. MTA1 is primarily localized in the nucleus but also found to be distributed in the extra-nuclear compartments. MTA1 is a component of several chromatin remodeling complexes including the nucleosome remodeling and deacetylation complex (NuRD). MTA1 regulates gene expression by functioning as a coregulator to integrate DNA-interacting factors to gene activity. MTA1 participates in physiological functions in the normal and cancer cells. MTA1 is one of the most upregulated proteins in human cancer and associates with cancer progression, aggressive phenotypes, and poor prognosis of cancer patients.

<span class="mw-page-title-main">CEBPD</span> Protein-coding gene in the species Homo sapiens

CCAAT/enhancer-binding protein delta is a protein that in humans is encoded by the CEBPD gene.

<span class="mw-page-title-main">CTBP1</span> Protein-coding gene in the species Homo sapiens

C-terminal-binding protein 1 also known as CtBP1 is a protein that in humans is encoded by the CTBP1 gene. CtBP1 is one of two CtBP proteins, the other protein being CtBP2.

<span class="mw-page-title-main">CUTL1</span> Protein-coding gene in the species Homo sapiens

Cux1 is a homeodomain protein that in humans is encoded by the CUX1 gene.

<span class="mw-page-title-main">ARID1A</span> Protein-coding gene in humans

AT-rich interactive domain-containing protein 1A is a protein that in humans is encoded by the ARID1A gene.

<span class="mw-page-title-main">MBD3</span> Protein-coding gene in the species Homo sapiens

Methyl-CpG-binding domain protein 3 is a protein that in humans is encoded by the MBD3 gene.

<span class="mw-page-title-main">PAX9</span> Protein-coding gene in humans

Paired box gene 9, also known as PAX9, is a protein which in humans is encoded by the PAX9 gene. It is also found in other mammals.

<span class="mw-page-title-main">MTA2</span> Protein-coding gene in the species Homo sapiens

Metastasis-associated protein MTA2 is a protein that in humans is encoded by the MTA2 gene.

<span class="mw-page-title-main">KDM5A</span> Protein-coding gene in the species Homo sapiens

Lysine-specific demethylase 5A is an enzyme that in humans is encoded by the KDM5A gene.

<span class="mw-page-title-main">Sp4 transcription factor</span> Protein-coding gene in the species Homo sapiens

Transcription factor Sp4 is a protein that in humans is encoded by the SP4 gene.

<span class="mw-page-title-main">KDM4A</span> Lysine-specific demethylase 4A is an enzyme that in humans is encoded by the Kdm4a gene

Lysine-specific demethylase 4A is an enzyme that in humans is encoded by the KDM4A gene.

<span class="mw-page-title-main">FOXG1</span> Protein-coding gene in the species Homo sapiens

Forkhead box protein G1 is a protein that in humans is encoded by the FOXG1 gene.

<span class="mw-page-title-main">Transcription initiation protein SPT3 homolog</span> Protein-coding gene in the species Homo sapiens

Transcription initiation protein SPT3 homolog is a protein that in humans is encoded by the SUPT3H gene.

<span class="mw-page-title-main">ARID4A</span> Protein-coding gene in humans

AT rich interactive domain 4A (RBP1-like), also known as ARID4A, is a protein which in humans is encoded by the ARID4A gene.

<span class="mw-page-title-main">ZNF350</span> Protein-coding gene in the species Homo sapiens

Zinc finger protein 350 is a protein that in humans is encoded by the ZNF350 gene.

<span class="mw-page-title-main">FOXA1</span> Protein-coding gene in the species Homo sapiens

Forkhead box protein A1 (FOXA1), also known as hepatocyte nuclear factor 3-alpha (HNF-3A), is a protein that in humans is encoded by the FOXA1 gene.

<span class="mw-page-title-main">KDM2B</span> Protein-coding gene in humans

The human KDM2B gene encodes the protein lysine (K)-specific demethylase 2B.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000117139 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000042207 - 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. Lahoud MH, Ristevski S, Venter DJ, Jermiin LS, Bertoncello I, Zavarsek S, Hasthorpe S, Drago J, de Kretser D, Hertzog PJ, Kola I (August 2001). "Gene targeting of Desrt, a novel ARID class DNA-binding protein, causes growth retardation and abnormal development of reproductive organs". Genome Research. 11 (8): 1327–34. doi: 10.1101/gr.168801 . hdl: 10536/DRO/DU:30121320 . PMID   11483573.
  6. Zhu L, Hu J, Lin D, Whitson R, Itakura K, Chen Y (August 2001). "Dynamics of the Mrf-2 DNA-binding domain free and in complex with DNA". Biochemistry. 40 (31): 9142–50. doi:10.1021/bi010476a. PMID   11478881.
  7. "Entrez Gene: JARID1B jumonji, AT rich interactive domain 1B".
  8. Kristensen LH, Nielsen AL, Helgstrand C, Lees M, Cloos P, Kastrup JS, Helin K, Olsen L, Gajhede M (June 2012). "Studies of H3K4me3 demethylation by KDM5B/Jarid1B/PLU1 reveals strong substrate recognition in vitro and identifies 2,4-pyridine-dicarboxylic acid as an in vitro and in cell inhibitor". The FEBS Journal. 279 (11): 1905–14. doi: 10.1111/j.1742-4658.2012.08567.x . PMID   22420752.
  9. Zou MR, Cao J, Liu Z, Huh SJ, Polyak K, Yan Q (June 2014). "Histone demethylase jumonji AT-rich interactive domain 1B (JARID1B) controls mammary gland development by regulating key developmental and lineage specification genes". The Journal of Biological Chemistry. 289 (25): 17620–33. doi: 10.1074/jbc.M114.570853 . PMC   4067197 . PMID   24802759.
  10. Albert M, Schmitz SU, Kooistra SM, Malatesta M, Morales Torres C, Rekling JC, Johansen JV, Abarrategui I, Helin K (April 2013). "The histone demethylase Jarid1b ensures faithful mouse development by protecting developmental genes from aberrant H3K4me3". PLOS Genetics. 9 (4): e1003461. doi: 10.1371/journal.pgen.1003461 . PMC   3630093 . PMID   23637629.
  11. 1 2 Tan K, Shaw AL, Madsen B, Jensen K, Taylor-Papadimitriou J, Freemont PS (June 2003). "Human PLU-1 Has transcriptional repression properties and interacts with the developmental transcription factors BF-1 and PAX9". The Journal of Biological Chemistry. 278 (23): 20507–13. doi: 10.1074/jbc.M301994200 . PMID   12657635.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.