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Long-read sequencing reveals increased isoform diversity in key transcription factor effectors of intercellular signalling at the invertebrate-vertebrate transition

Abstract:

Several intercellular signalling pathways (namely wingless - Wnt, Hedgehog - Hh, and Bone Morphogenetic Protein - BMP) are used repeatedly in animals throughout development and evolution, and are also frequent targets for disease-associated disruptions. We have previously shown that the major transcriptional effectors of βcatenin-dependent Wnt signalling, the TCF/LEF proteins, in contrast to other pathway components, have a higher gene number and isoform diversity in vertebrates versus invertebrates, but this increased diversity has only been poorly quantified. Considering that isoform diversity correlates with organism complexity, any increase in major signalling effectors is likely to have made a significant contribution to vertebrate evolution. Using de novo long-read transcriptomes, we compared isoform number per gene for the chordates Ciona intestinalis, Lampetra planeri and Xenopus tropicalis, thus encompassing the invertebrate sister group to vertebrates, as well as a cyclostome and a gnathostome vertebrate. Our results implicate an increase in isoform diversity of the transcription factors of major intercellular signalling pathways as having a disproportionate role in the evolutionary origin and diversification of vertebrates.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1186/s12915-026-02522-w

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Biology
Oxford college:
Balliol College
Role:
Author
ORCID:
0000-0003-0195-7536


More from this funder
Funder identifier:
https://ror.org/00cwqg982
Grant:
BB/X015203/1


Publisher:
Springer
Journal:
BMC Biology More from this journal
Volume:
24
Issue:
1
Article number:
28
Publication date:
2026-01-24
Acceptance date:
2026-01-16
DOI:
EISSN:
1741-7007


Language:
English
Keywords:
Pubs id:
2357275
Local pid:
pubs:2357275
Deposit date:
2026-01-09
ARK identifier:

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