共 75 条
How to make ends meet in V(D)J recombination
被引:45
作者:

Grawunder, U
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机构:
Univ Ulm Klinikum, Dept Immunol, D-89081 Ulm, Germany Univ Ulm Klinikum, Dept Immunol, D-89081 Ulm, Germany

Harfst, E
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Univ Ulm Klinikum, Dept Immunol, D-89081 Ulm, Germany Univ Ulm Klinikum, Dept Immunol, D-89081 Ulm, Germany
机构:
[1] Univ Ulm Klinikum, Dept Immunol, D-89081 Ulm, Germany
关键词:
D O I:
10.1016/S0952-7915(00)00203-X
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
In most vertebrate species analyzed so far, the diversity of soluble or membrane-bound antigen-receptors expressed by B and T lymphocytes is generated by V(D)J recombination. During this process, the coding regions for the variable domains of antigen-receptors are created by the joining of subexons that are randomly selected from arrays of tandemly repeated V, D (sometimes) and J gene segments. This involves the site-specific cleavage of chromosomal DNA by the lymphocyte-specific recombination-activating gene (RAG)-1/2 proteins, which appear to have originated from an ancient transposable element. The DNA double-strand breaks created by RAG proteins are subsequently processed and rejoined by components of the nonhomologous DNA end-joining pathway, which is conserved in all eukaryotic organisms - from unicellular yeast up to highly complex mammalian species.
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页码:186 / 194
页数:9
相关论文
共 75 条
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