KDM2B Recombinant Rabbit Monoclonal Antibody [PSH05-38] (HA722267)

UNIPROT #

Q8NHM5

PROTEIN NAME

KDM2B

SYNONYMS

[Histone-H3]-lysine-36 demethylase 1B antibody;CXXC-type zinc finger protein 2 antibody;CXXC2 antibody;F box and leucine rich repeat protein 10 antibody;F box protein FBL10 antibody;F-box and leucine-rich repeat protein 10 antibody;F-box protein FBL10 antibody;F-box/LRR-repeat protein 10 antibody;Fbl10 antibody;FBXL10 antibody;JEMMA (Jumonji domain EMSY interactor methyltransferase motif) protein antibody;JHDM1B antibody;JmjC domain-containing histone demethylation protein 1B antibody;Jumonji C domain containing histone demethylase 1B antibody;Jumonji domain-containing EMSY-interactor methyltransferase motif protein antibody;kdm2b antibody;KDM2B_HUMAN antibody;Lysine (K) specific demethylase 2B antibody;Lysine-specific demethylase 2B antibody;PCCX2 antibody;Protein containing CXXC domain 2 antibody;Protein JEMMA antibody;Protein-containing CXXC domain 2 antibody

SUBCELLULAR LOCATION

Nucleus, nucleolus, Chromosome.

FUNCTION

This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class. Multiple alternatively spliced transcript variants have been found for this gene, but the full-length nature of some variants has not been determined. As part of the ncPRC1.1 complex, KDM2B was found to be rapidly and transiently recruited to sites of DNA damage in a PARP1- and TIMELESS-dependent manner to promote mono-ubiquitylation of histone H2A on K119 with concomitant local decrease of H2A levels and an increase of H2A.Z. These events promote transcriptional repression at DNA lesions, double strand break signaling, and homologous recombination repair. The activity of the ncPRC1.1 complex at DNA lesions was necessary for the proper recruitment of the two canonical PRC1 complexes (cPRC1.2 and cPRC1.4), defined by their PCGF subunits, MEL18 and BMI1 respectively. Therefore, recruitment of the ncPRC1.1 complex represents an early and critical regulatory step in homologous recombination repair.