DNA polymerases ν and θ are required for efficient immunoglobulin V gene diversification in chicken

Author:

Kohzaki Masaoki123,Nishihara Kana14,Hirota Kouji1,Sonoda Eiichiro1,Yoshimura Michio1,Ekino Shigeo5,Butler John E.6,Watanabe Masami2,Halazonetis Thanos D.3,Takeda Shunichi1

Affiliation:

1. Department of Radiation Genetics and Department of Radiation Oncology and Image-Applied Therapy, Graduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan

2. Research Reactor Institute, Kyoto University, Sennan-gun, Osaka 590-0494, Japan

3. Department of Molecular Biology, University of Geneva, Geneva 4 CH-1211, Switzerland

4. Department of Food and Nutrition, Kyoto Women’s University, Higashiyama-ku, Kyoto 606-8501, Japan

5. Department of Histology, Graduate School of Medical Sciences, Kumamoto University, Honjo, Kumamoto 860-8556, Japan

6. Department of Microbiology, University of Iowa Medical School, Iowa City, IA 52242

Abstract

The chicken DT40 B lymphocyte line diversifies its immunoglobulin (Ig) V genes through translesion DNA synthesis–dependent point mutations (Ig hypermutation) and homologous recombination (HR)–dependent Ig gene conversion. The error-prone biochemical characteristic of the A family DNA polymerases Polν and Polθ led us to explore the role of these polymerases in Ig gene diversification in DT40 cells. Disruption of both polymerases causes a significant decrease in Ig gene conversion events, although POLN−/−/POLQ−/− cells exhibit no prominent defect in HR-mediated DNA repair, as indicated by no increase in sensitivity to camptothecin. Polη has also been previously implicated in Ig gene conversion. We show that a POLH−/−/POLN−/−/POLQ−/− triple mutant displays no Ig gene conversion and reduced Ig hypermutation. Together, these data define a role for Polν and Polθ in recombination and suggest that the DNA synthesis associated with Ig gene conversion is accounted for by three specialized DNA polymerases.

Publisher

Rockefeller University Press

Subject

Cell Biology

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