Sandbox GGC9
Structure of RAG1/2-DNA Strand Transfer Complex (paired conformation)Structure of RAG1/2-DNA Strand Transfer Complex (paired conformation)
RAG1 is the catalytic component of the RAG Complex. Together with RAG2, the RAG Complex functions to create antibodies for virtually any antigen. FunctionRAG1 and RAG2 form the RAG Complex (RAG Recombinases), which is responsible for regulating the DNA cleavage phase during recombination. V(D)J recombination functions to produce a plethora of immune molecules in developing B and T-lymphocytes. The V stands for variable, D, diversity and J joining of the gene segments. RAG1 functions as the catalytic portion while RAG2, although not catalytic, is required for RAG1 to function.[1] RAG1 controls the ability of the DNA to bind to the RSS or recombination signal sequences. This is achieved by the ability of the RAG1 complex to create a double-stranded break between the (RSS) and the adjacent coding sequence. This process is executed in the following way: introduction of a nick, creating a 3'-hydroxyl group which attacks the phosphodiester bond on the opposite strand.[1] This is a direct transesterification reaction which results in four DNA ends. Histones also assist in the nicking and hairpinning of the strands. The result is the recombination of variable genes joining.[1] Additionally to the role played in V(D)J, RAG also assists in pre-B cell allelic exclusion. This means that there is a recombination of the second allele. RAG1 also possess ubiquitin properties. Newer Studies suggest that the RAG1/2 recombinase complex acts as a domesticated transposase.[2] DiseaseMutations of the RAG recombinases are often occurring in patients being displaying immunodeficiency and Omenn syndrome. [3] Omenn's syndrome is a severe combined immunodeficiency. [4] Some characteristics include redness of skin, peeling skin, hair loss, chronic diarrhea, enlarged lymph nodes, swelling of liver and spleen, and increased levels of of serum IgE. [4]
(Hsu et al 2011) RelevanceEarly intervention of people with Omenn's syndrome is important, because if left untreated it will be fatal. [4] Treatment of Omenn's syndrome includes bone marrow or cord blood stem cell transplantation. [4] Structural highlightsThe subunit structure is defined as a homodimer. The zinc site plays an important role in DNA cleavage; without the zinc site the DNA would not be able to be cleaved and would not form the essential hairpin structure.[5]
Recent studies identified aspartic acid residues at positions 600 and 708 function to initiate catalysis.[7]
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ReferencesReferences
[1] Grazini U, Zanardi F, Citterio E, Casola S, Goding CR, McBlane F. The RING domain of RAG1 ubiquitylates histone H3: a novel activity in chromatin-mediated regulation of V(D)J joining. Mol Cell. 2010 Jan 29;37(2):282-93. doi: 10.1016/j.molcel.2009.12.035. PMID: 20122409.
[2] Zhang Y, Corbett E, Wu S, Schatz DG. Structural basis for the activation and suppression of transposition during evolution of the RAG recombinase. EMBO J. 2020 Nov 2;39(21):e105857. doi: 10.15252/embj.2020105857. Epub 2020 Sep 18. PMID: 32945578; PMCID: PMC7604617.
[3] Chen, Karin et al. “Autoimmunity due to RAG deficiency and estimated disease incidence in RAG1/2 mutations.” The Journal of allergy and clinical immunology vol. 133,3 (2014): 880-2.e10. doi:10.1016/j.jaci.2013.11.038
[4] Omenn syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. Rarediseases.info.nih.gov. (2021). Retrieved 7 April 2021, from https://rarediseases.info.nih.gov/diseases/8198/omenn-syndrome.
[5] Gwyn, Lori M et al. “A zinc site in the C-terminal domain of RAG1 is essential for DNA cleavage activity.” Journal of molecular biology vol. 390,5 (2009): 863-78. doi:10.1016/j.jmb.2009.05.076
[6] Hsu, C., Yu-Yun Lee, J., & Chao, S. (2011). Omenn syndrome: a case report and review of literature. Dermatologica Sinica, 29(2). https://doi.org/doi.org/10.1016/j.dsi.2011.05.002
[7] Fugmann, S., Villey, I., Ptaszek, L., & Schatz, D. (2000). Identification of Two Catalytic Residues in RAG1 that Define a Single Active Site within the RAG1/RAG2 Protein Complex. Molecular Cell, 5(1), 97-107. https://doi.org/10.1016/s1097-2765(00)80406-2