Abstract
Although it is generally accepted that Ig heavy chains (HC) are selected at the pre-B cell receptor (pre-BCR) checkpoint, the characteristics of a functional HC and the role of pre-BCR assembly in their selection have remained elusive. We determined the characteristics of HCs that successfully passed the pre-BCR checkpoint by examining transcripts harboring V(H)81X and J(H)4 gene segments from J(H)(+/-) and lambda5(-/-)mice. V(H)81X-J(H)4-HC transcripts isolated from cells before or in the absence of pre-BCR assembly had no distinguishing complementarity-determining region 3 traits. In contrast, transcripts isolated subsequent to passage through the pre-BCR checkpoint had distinctive complementarity-determining regions 3 of nine amino acids in length (49%) and a histidine at position 1 (73%). Hence, our data define specific structural requirements for a functional HC, which is instrumental in shaping the diverse B cell repertoire.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acids / analysis*
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Amino Acids / genetics
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Animals
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B-Lymphocyte Subsets / cytology
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B-Lymphocyte Subsets / immunology
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B-Lymphocyte Subsets / metabolism
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Bone Marrow Cells / cytology
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Bone Marrow Cells / immunology
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Bone Marrow Cells / metabolism
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Cell Differentiation / genetics
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Cell Differentiation / immunology
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Cell Membrane / genetics
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Cell Membrane / immunology
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Cell Membrane / metabolism
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Complementarity Determining Regions / biosynthesis*
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Complementarity Determining Regions / genetics
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Complementarity Determining Regions / physiology
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Gene Rearrangement, B-Lymphocyte, Heavy Chain
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Histidine / analysis
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Histidine / genetics
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Immunoglobulin Heavy Chains / biosynthesis*
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Immunoglobulin Heavy Chains / genetics
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Immunoglobulin Heavy Chains / physiology
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Immunoglobulin Light Chains
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Immunoglobulin Light Chains, Surrogate
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Immunoglobulin mu-Chains / biosynthesis*
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Immunoglobulin mu-Chains / genetics
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Immunoglobulin mu-Chains / physiology
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Membrane Glycoproteins / deficiency
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Membrane Glycoproteins / genetics
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Membrane Glycoproteins / physiology
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Mice
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Mice, Inbred C57BL
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Mice, Knockout
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Models, Immunological
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Models, Molecular
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Peptide Fragments / biosynthesis*
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Peptide Fragments / genetics
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Peptide Fragments / physiology
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Protein Processing, Post-Translational / genetics
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Protein Processing, Post-Translational / immunology*
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Protein Structure, Tertiary
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Spleen / cytology
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Spleen / immunology
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Spleen / metabolism
Substances
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Amino Acids
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Complementarity Determining Regions
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Immunoglobulin Heavy Chains
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Immunoglobulin Light Chains
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Immunoglobulin Light Chains, Surrogate
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Immunoglobulin mu-Chains
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Membrane Glycoproteins
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Peptide Fragments
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Histidine