RAG2

Recombination activating gene 2

Identifiers

RAG2 ; RAG-2

External IDs

OMIM: 179616 HomoloGene: 7507 GeneCards: RAG2 Gene

Gene ontology
Molecular function	• DNA binding • chromatin binding • phosphatidylinositol-4,5-bisphosphate binding • phosphatidylinositol-3,4,5-trisphosphate binding • zinc ion binding • methylated histone binding • phosphatidylinositol binding • phosphatidylinositol-3,4-bisphosphate binding • ubiquitin protein ligase activity • phosphatidylinositol-3,5-bisphosphate binding
Cellular component	• nucleus
Biological process	• B cell lineage commitment • pre-B cell allelic exclusion • B cell homeostatic proliferation • T cell lineage commitment • protein ubiquitination • chromatin modification • B cell differentiation • T cell differentiation in thymus • V(D)J recombination • positive regulation of organ growth
Sources: Amigo / QuickGO

Orthologs

Species

Human

Mouse

RefSeq (mRNA)

RefSeq (protein)

Location (UCSC)

Chr 11:
36.58 – 36.6 Mb

Chr 2:
101.62 – 101.63 Mb

PubMed search

Recombination activating gene 2 also known as RAG-2 is a protein that in humans is encoded by the RAG2 gene.^[1]

Function

This gene encodes a protein that is involved in the initiation of V(D)J recombination during B and T cell development. This protein forms a complex with the product of the adjacent recombination activating gene 1, and this complex can form double-strand breaks by cleaving DNA at conserved recombination signal sequences. The recombination activating gene 1 component is thought to contain most of the catalytic activity, while the N-terminal of the recombination activating gene 2 component is thought to form a six-bladed propeller in the active core that serves as a binding scaffold for the tight association of the complex with DNA. A C-terminal plant homeodomain finger-like motif in this protein is necessary for interactions with chromatin components, specifically with histone H3 that is trimethylated at lysine 4.

Clinical significance

Mutations in this gene cause Omenn syndrome, a form of severe combined immunodeficiency associated with autoimmune-like symptoms.^[1]

References

1 2 "Entrez Gene: Recombination activating gene 2".

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

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