Document details

iRAGu: A Novel Inducible and Reversible Mouse Model for Ubiquitous Recombinase Activity

Author(s): Bonnet, Marie ; Sarmento, Leonor Morais ; Martins, Ana C. ; Sobral, Daniel ; Silva, Joana ; Demengeot, Jocelyne

Date: 2017

Persistent ID: http://hdl.handle.net/10400.7/813

Origin: ARCA - Access to Research and Communication Annals

Project/scholarship: info:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBIA-GEN%2F116830%2F2010/PT;

Subject(s): recombination activating gene; transgenic mouse model; 4-hydroxytamoxifen induction; estrogen receptor; lymphocyte development; V(D)J recombination


Description

This deposit is composed by the main article plus the supplementary materials of the publication.

Developing lymphocytes express the recombination activating genes (RAGs) 1 and 2 products that form a site specific recombinase complex (RAG), introducing double strand DNA breaks (DSBs) at recombination signal sequences (RSSs) flanking the V, D, and J gene segments in the antigen receptor loci. The subsequent steps in the reaction consist in the ligation of DSBs by ubiquitous enzymes of the non-homologous end joining DNA repair pathway. This mutagenesis process is responsible for the generation of the very large clonal diversity of T and B lymphocytes, itself allowing the recognition of a virtually open-ended antigenic universe. Sequences resembling RSS are found at high frequency all over the genome, and involved in RAG mediated illegitimate recombination and translocations. Hence, natural and induced ectopic activity of RAG is a threat to the genome only recently underscored. Here, we report and characterize a novel mouse transgenic system for which ubiquitous expression of the recombinase is inducible. In this system, the RAG1 protein is constitutively expressed and functional, while the RAG2 protein, coupled to the estrogen receptor, becomes functionally active upon 4-hydroxytamoxifen (TAM) administration. We describe two transgenic lines. The first one, when introgressed into an endogenous Rag2−/− genetic background is faithfully recapitulating lymphocyte development, repertoire dynamics and cryptic rearrangements, in a TAM-dependent manner. In this model, deprivation of TAM is followed by lymphocyte development arrest, evidencing the reversibility of the system. The second transgenic line is leaky, as the transgenes promote lymphocyte differentiation in absence of TAM treatment. Upon TAM-induction defects in lymphocytes composition and global health reveals the deleterious effect of uncontrolled RAG activity. Overall, this novel transgenic model provides a tool where RAG activity can be specifically manipulated to assess the dynamics of lymphocyte differentiation and the challenges imposed by the recombinase on the vertebrate genome.

Fundação para a Ciência e a Tecnologia grants: (PTDC/BIA-GEN/116830/2010, fellowships); Portuguese League Against Cancer; Terry Fox Foundation.

Document Type Journal article
Language English
Contributor(s) ARCA
CC Licence
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