Taylor F. Dawson
Gene Splicing of an Invertebrate Beta Subunit (LCavβ) in the N-Terminal and HOOK Domains and Its Regulation of LCav1 and LCav2 Calcium Channels
Dawson, Taylor F.; Boone, Adrienne N.; Senatore, Adriano; Piticaru, Joshua; Thiyagalingam, Shano; Jackson, Daniel; Davidson, Angus; Spafford, J. David
Authors
Adrienne N. Boone
Adriano Senatore
Joshua Piticaru
Shano Thiyagalingam
Daniel Jackson
ANGUS DAVISON angus.davison@nottingham.ac.uk
Professor of Evolutionary Genetics
J. David Spafford
Contributors
Alexander G. Obukhov
Editor
Abstract
The accessory beta subunit (Cavβ) of calcium channels first appear in the same genome as Cav1 L-type calcium channels in single-celled coanoflagellates. The complexity of this relationship expanded in vertebrates to include four different possible Cavβ subunits (β1, β2, β3, β4) which associate with four Cav1 channel isoforms (Cav1.1 to Cav1.4) and three Cav2 channel isoforms (Cav2.1 to Cav2.3). Here we assess the fundamentally-shared features of the Cavβ subunit in an invertebrate model (pond snail Lymnaea stagnalis) that bears only three homologous genes: (LCav1, LCav2, and LCavβ). Invertebrate Cavβ subunits (in flatworms, snails, squid and honeybees) slow the inactivation kinetics of Cav2 channels, and they do so with variable N-termini and lacking the canonical palmitoylation residues of the vertebrate β2a subunit. Alternative splicing of exon 7 of the HOOK domain is a primary determinant of a slow inactivation kinetics imparted by the invertebrate LCavβ subunit. LCavβ will also slow the inactivation kinetics of LCav3 T-type channels, but this is likely not physiologically relevant in vivo. Variable N-termini have little influence on the voltage-dependent inactivation kinetics of differing invertebrate Cavβ subunits, but the expression pattern of N-terminal splice isoforms appears to be highly tissue specific. Molluscan LCavβ subunits have an N-terminal “A” isoform (coded by exons: 1a and 1b) that structurally resembles the muscle specific variant of vertebrate β1a subunit, and has a broad mRNA expression profile in brain, heart, muscle and glands. A more variable “B” N-terminus (exon 2) in the exon position of mammalian β3 and has a more brain-centric mRNA expression pattern. Lastly, we suggest that the facilitation of closed-state inactivation (e.g. observed in Cav2.2 and Cavβ3 subunit combinations) is a specialization in vertebrates, because neither snail subunit (LCav2 nor LCavβ) appears to be compatible with this observed property.
Citation
Dawson, T. F., Boone, A. N., Senatore, A., Piticaru, J., Thiyagalingam, S., Jackson, D., …Spafford, J. D. (2014). Gene Splicing of an Invertebrate Beta Subunit (LCavβ) in the N-Terminal and HOOK Domains and Its Regulation of LCav1 and LCav2 Calcium Channels. PLoS ONE, 9(4), 1-17. https://doi.org/10.1371/journal.pone.0092941
Journal Article Type | Article |
---|---|
Acceptance Date | Feb 27, 2014 |
Online Publication Date | Apr 1, 2014 |
Publication Date | Apr 1, 2014 |
Deposit Date | Dec 22, 2017 |
Publicly Available Date | Jul 31, 2019 |
Journal | PLoS ONE |
Electronic ISSN | 1932-6203 |
Publisher | Public Library of Science |
Peer Reviewed | Peer Reviewed |
Volume | 9 |
Issue | 4 |
Article Number | e92941 |
Pages | 1-17 |
DOI | https://doi.org/10.1371/journal.pone.0092941 |
Public URL | ://WOS:000334101100036 |
Publisher URL | https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0092941 |
Contract Date | Jul 31, 2019 |
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Gene Splicing of an Invertebrate Beta Subunit (LCavβ) in the N-Terminal and HOOK Domains and Its Regulation of LCav1 and LCav2 Calcium Channels
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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