In this work we present the successful generation and application of hiPSC based disease models for isoform studies using the EXSISERS, building the basis of further use of the model for disease related investigation in a human genetic background. We show evidence implicating Class I and IV HDAC involvement in
MAPT alternative splicing under physiological conditions. Furthermore, a novel regulation of
MAPT exon 10 mRNA translation was shown indicating a FABP involvement in translational regulation.
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In this work we present the successful generation and application of hiPSC based disease models for isoform studies using the EXSISERS, building the basis of further use of the model for disease related investigation in a human genetic background. We show evidence implicating Class I and IV HDAC involvement in
MAPT alternative splicing under physiological conditions. Furthermore, a novel regulation of
MAPT exon 10 mRNA translation was shown indicating a FABP involvement in translational regulati...
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