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      Selection of Ig mu heavy chains by complementarity-determining region 3 length and amino acid composition.

      The Journal of Immunology Author Choice
      Amino Acids, analysis, genetics, Animals, B-Lymphocyte Subsets, cytology, immunology, metabolism, Bone Marrow Cells, Cell Differentiation, Cell Membrane, Complementarity Determining Regions, biosynthesis, physiology, Gene Rearrangement, B-Lymphocyte, Heavy Chain, Histidine, Immunoglobulin Heavy Chains, Immunoglobulin Light Chains, Immunoglobulin Light Chains, Surrogate, Immunoglobulin mu-Chains, Membrane Glycoproteins, deficiency, Mice, Mice, Inbred C57BL, Mice, Knockout, Models, Immunological, Models, Molecular, Peptide Fragments, Protein Processing, Post-Translational, Protein Structure, Tertiary, Spleen

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          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.

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