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

BMC Genomics. 2022 Jan 10;23(1):42. doi: 10.1186/s12864-021-08261-2.

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.

MeSH terms

  • Alternative Splicing
  • Animals
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Nanopores*
  • Protein Isoforms / genetics
  • RNA Splicing*

Substances

  • Protein Isoforms