4.6 Article

Nanopore Sequencing Unveils Diverse Transcript Variants of the Epithelial Cell-Specific Transcription Factor Elf-3 in Human Malignancies

Journal

GENES
Volume 12, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/genes12060839

Keywords

alternative splicing; nanopore sequencing; transcription factor; long-read sequencing; transcriptome; ETS transcription factor 3 (Elf-3)

Funding

  1. Bodossaki Foundation (Athens, Greece)

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Elf-3, a member of the ETS family, is crucial in epithelial cell differentiation, development, and cancer. This study identified 25 new ELF3 mRNA transcript variants and two novel exons, laying the foundation for further research on the biological function of these variants and protein isoforms.
The human E74-like ETS transcription factor 3 (Elf-3) is an epithelium-specific member of the ETS family, all members of which are characterized by a highly conserved DNA-binding domain. Elf-3 plays a crucial role in epithelial cell differentiation by participating in morphogenesis and terminal differentiation of the murine small intestinal epithelium, and also acts as an indispensable regulator of mesenchymal to epithelial transition, underlying its significant involvement in development and in pathological states, such as cancer. Although previous research works have deciphered the functional role of Elf-3 in normal physiology as well as in tumorigenesis, the present study highlights for the first time the wide spectrum of ELF3 mRNAs that are transcribed, providing an in-depth analysis of splicing events and exon/intron boundaries in a broad panel of human cell lines. The implementation of a versatile targeted nanopore sequencing approach led to the identification of 25 novel ELF3 mRNA transcript variants (ELF3 v.3-v.27) with new alternative splicing events, as well as two novel exons. Although the current study provides a qualitative transcriptional profile regarding ELF3, further studies must be conducted, so the biological function of all novel alternative transcript variants as well as the putative protein isoforms are elucidated.

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