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      Identification and comparative analysis of Pax5 C-terminal isoforms expressed in human cord blood-derived B cell progenitors.

      Immunology Letters

      Antigens, CD34, metabolism, B-Cell-Specific Activator Protein, genetics, B-Lymphocytes, cytology, immunology, Base Sequence, Cell Differentiation, Cell Line, Cells, Cultured, Reverse Transcriptase Polymerase Chain Reaction, Cloning, Molecular, Female, Fetal Blood, Humans, Molecular Sequence Data, Pregnancy, Protein Isoforms, Alternative Splicing

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          We identified three Pax5 isoforms due to alternative splicing of the C-terminal exons of its gene in cord blood (CB)-derived B cell progenitors cultivated on the murine bone marrow stromal (HESS-5) cells. Apart from wild type (wt), one isoform skips exon 9 without subsequent frameshift (del9), while the other has a frameshift insert between exons 8 and 9, resulting in novel C-terminal sequences (ins8'). Quantitative reverse transcription-polymerase chain reaction analysis revealed that wt mRNA could be detected in CB CD34(+) cells, but that del9 and ins8' isoforms only appeared after 1 or 3 weeks of co-culture, respectively. Expression of each isoform mRNA was markedly upregulated during B cell differentiation in vitro, and wild type continued to be the most abundant isoform. In a luciferase reporter assay using a synthetic CD19 enhancer, del9 isoform revealed slightly lower activity and ins8' isoform showed much lower activity, compared with Pax5-wt. Furthermore, retroviral expression of each Pax5 isoform in CB CD34(+) cells induced aberrant CD19 expression in a fraction of immature myeloid cells after 1 week of culture, although del9 and ins8' isoforms showed much less potent activity than Pax5-wt. These results suggest that Pax5-wt is quantitatively and qualitatively dominant over other C-terminal isoforms during human B cell differentiation.

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