Abstract
The joining of DNA ends during Ig class-switch recombination (CSR) is thought to involve the same nonhomologous end-joining pathway as used in V(D)J recombination. However, we reported earlier that CSR can readily occur in Ig transgenic SCID mice lacking DNA-dependent protein kinase (DNA-PK) activity, a critical enzymatic activity for V(D)J recombination. We were thus led to question whether the catalytic subunit of DNA-PK (DNA-PKcs) is essential for CSR. To address this issue, we asked whether class switching to different Ig isotypes could occur in a line of Ig transgenic mice lacking detectable DNA-PKcs protein. The answer was affirmative. We conclude that joining of DNA ends during CSR does not require DNA-PKcs and can occur by an alternative repair pathway to that used for V(D)J recombination.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Adoptive Transfer
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Animals
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B-Lymphocytes / cytology
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Bone Marrow Cells / cytology
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Breeding
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Catalytic Domain*
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Cell Count
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DNA-Activated Protein Kinase / deficiency
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DNA-Activated Protein Kinase / metabolism*
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DNA-Binding Proteins / deficiency
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DNA-Binding Proteins / metabolism*
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Flow Cytometry
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Genotype
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Immunoglobulin Class Switching / genetics*
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Immunoglobulin Class Switching / immunology*
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Immunoglobulins / blood
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Mice
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Mice, SCID
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Mice, Transgenic
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Nuclear Proteins / deficiency
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Nuclear Proteins / metabolism*
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Recombination, Genetic*
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Spleen / cytology
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T-Lymphocytes / cytology
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Thymus Gland / cytology
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Transgenes
Substances
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DNA-Binding Proteins
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Immunoglobulins
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Nuclear Proteins
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DNA-Activated Protein Kinase
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Prkdc protein, mouse