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Shimeld, S.

Publications and source records attributed to Shimeld, S..

2 recordsLinked to original sources

Long-Read Sequencing Reveals Increased Isoform Diversity in Key Transcription Factor Effectors of Intercellular Signalling at the Invertebrate-Vertebrate Transition

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 {beta}-catenin-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.

evolutionary biology↗

A microfluidic device for controlled exposure of transgenic Ciona intestinalis larvae to chemical stimuli demonstrates they can respond to carbon dioxide.

The larva of the ascidian Ciona intestinalis controls a small repertoire of behaviours with a simple nervous system in which each cell is identifiable. As such it offers the prospect of building a cohesive cell-level picture of how a nervous system integrates sensory inputs to produce specific behavioural outcomes. Here, we report the development of a microfluidic chip in which larvae can be immobilised and exposed to chemical stimuli. We generate transgenic larvae in which the calcium ion reporter GCaMP6m is expressed in a defined population of cells, allowing us to record real-time neural activity following stimulation. We then use this to establish that some cell populations can sense dissolved carbon dioxide. We also leverage genome and transcriptome data coupled with molecular evolutionary analysis to identify putative chemoreceptors of the MS4A family in Ciona. Our study demonstrates that Ciona larvae can respond to dissolved carbon dioxide, identifies the cells that are likely responsible for chemosensation, and establishes a chip based imaging platform coupled with transgenic technology that could be adapted to establish where other stimuli are sensed and how such incoming signals are processed in the brain to yield behavioural output.

evolutionary biology↗