Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes

长读长测序揭示了新的异构体,并深入了解了细胞状态变化过程中剪接调控的机制

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作者:David J Wright ,Nicola A L Hall ,Naomi Irish ,Angela L Man ,Will Glynn ,Arne Mould ,Alejandro De Los Angeles ,Emily Angiolini ,David Swarbreck ,Karim Gharbi ,Elizabeth M Tunbridge ,Wilfried Haerty

Abstract

Background: Alternative splicing is a key mechanism underlying cellular differentiation and a driver of complexity in mammalian neuronal tissues. However, understanding of which isoforms are differentially used or expressed and how this affects cellular differentiation remains unclear. Long read sequencing allows full-length transcript recovery and quantification, enabling transcript-level analysis of alternative splicing processes and how these change with cell state. Here, we utilise Oxford Nanopore Technologies sequencing to produce a custom annotation of a well-studied human neuroblastoma cell line SH-SY5Y, and to characterise isoform expression and usage across differentiation. Results: We identify many previously unannotated features, including a novel transcript of the voltage-gated calcium channel subunit gene, CACNA2D2. We show differential expression and usage of transcripts during differentiation identifying candidates for future research into state change regulation. Conclusions: Our work highlights the potential of long read sequencing to uncover previously unknown transcript diversity and mechanisms influencing alternative splicing.

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