Immunoglobulin gene conversion and somatic hypermutation: regulation, evolution and biotechnology Center for Developmental Biology

Home > Seminars and Events > Immunoglobulin gene conversion and somatic hypermutation: regulation, evolution and biotechnology

Category	Seminar
Date and Time	2011-09-14 16:00 - 17:00
Venue	Seminar Room A7F
Speaker	Hiroshi Arakawa
Affiliation	Max Planck Institute of Biochemistry, Martinsried, Germany
Title	Immunoglobulin gene conversion and somatic hypermutation: regulation, evolution and biotechnology
Poster	click here to download(PDF)
Host	Masatoshi Takeichi
Summary	Immunoglobulin (Ig) genes of chicken are diversified by segmental gene conversion using pseudo V genes as donors. Our lab has studied molecular mechanisms of post V (D) J diversification using chicken B cell line DT40, which has gene conversion activity and high ratios of targeted integration. We have shown that activation-induced cytidine deaminase (AID), the key regulator of class switch recombination and somatic hypermutation, is required for gene conversion, and it meant that all the three post V (D) J re-modelling systems depend on AID. Interestingly, knockout of the pseudo gene donors changes Ig gene diversification system of DT40 from gene conversion to somatic hypermutation, indicating that these two different diversification systems are related and competing pathways with each other. In this seminar I will review recent topics of our research on gene conversion and hypermutation: especially about their mechanism and regulation, evolution of Ig gene diversification system, and application of Ig gene diversification system for bio technology.