Luis Guerra

@luisguerra.bsky.social

Lecturer/Assistant Professor in Pharmacology. Interest: Neurobiology, the evolution of the nervous system, GPCR deorphanisation, non-bilaterians.

Prebilaterian Origin of Monoaminergic Signalling is out! This paper represents four years of work, not only mine, but friends and colleagues. I am particularly grateful to Tatiana Mayorova; without her help, this paper would not have been nearly as complete. www.sciencedirect.com/science/arti...

Prebilaterian origin of monoaminergic signaling

Monoamines such as serotonin, dopamine, and tyramine regulate physiological and behavioral processes in bilaterian animals, but the evolutionary origi…

sciencedirect.com

My collaborator in France, Luis Bezares, is recruiting for our HFSP project on the evolutionary origins of TRP channel-mediated sensation. Interested in sensory biology, behaviour, microscopy, live imaging and early animal evolution? Join the Plankton Senses team in Villefranche-sur-Mer.

Luis Alberto Bezares Calderón@lbezarescalderon.bsky.social · 2mo ago

I'm recruiting a postdoc and a research assistant in my lab in the south of France for an HFSP-funded project involving choanos. More info: Postdoc: bit.ly/4xxlJTX Research assistant: (EN) bit.ly/4aOwUha (FR) bit.ly/4vcy3av Please share with any potential applicant. Thx!

Genuinely fascinating topic. But all I could see was plankton from SpongeBob. 😂

Plankton from Spongebob Sitting

ALT: Plankton from Spongebob Sitting

static.klipy.com

PLOS Biology@plosbiology.org · 2mo ago

What are the mechanisms allowing #zebrafish to #regenerate their neurons after spinal cord injury? This study by @albertodseara.bsky.social , Catherine Becker, Thomas Becker &co shows that a protein in #microglia regulates regenerative #neurogenesis in multiple ways 🧪#AcademicSky plos.io/4xy2CcB

A graphical summary of proposed interactions of sema4ab during spinal cord regeneration. After spinal injury, microglia likely control neurogenesis directly by signaling through Sema4ab and Plxnb1a/b on ependymo-radial glial cells (ERGs), and indirectly by changing the injury site environment, which leads to lower expression of tgfb3, a positive regulator of regenerative neurogenesis, in fibroblasts. Additionally, Sema4ab controls microglia number by promoting cell proliferation.

This paper is the result of funding from the BBSRC that I received in 2022 for my independent research. Then, since 2023, I’ve led my own lab focused on receptor deorphanisation and evolution of the nervous system, If you're interested in large-scale GPCR testing or collaborations, get in touch!

Gaspar Jekely@jekely.biologists.social.ap.brid.gy · last yr.

New insights into neurotransmitter evolution from a GPCR screen in Trichoplax, a neuron-less animal. with Yanez-Guerra et al. https://www.biorxiv.org/content/10.1101/2025.04.18.649542v1 Trichoplax has tryptamine, tyramine, and phenethylamine receptors […] [Original post on biologists.social]

Synthesis pathway of
placozoan monoamine receptor agonists compared to the acetylated versions
of the compounds that activate human melatonin receptors

Preprint alert!. In the most recent work of my laboratory, we demonstrate that placozoans are able to respond to monoamines, furthermore, we experimentally characterise the receptors responsible for these effects. #Science #Placozoans #Neurotransmitters #Monoamines www.biorxiv.org/content/10.1...

Functional and phylogenetic analysis of placozoan GPCRs reveal the prebilaterian origin of monoaminergic signalling.

Monoamines are biologically active compounds crucial for neurotransmission and various physiological processes. They include neurotransmitters like serotonin, dopamine, and melatonin, which regulate mood, movement, and sleep in humans. In ecdysozoans, monoamines such as tyramine are important for modulating locomotion, learning, and feeding. The monoaminergic signalling system has been considered a bilaterian innovation, with conflicting evidence supporting its existence in earlier branching, non-bilaterian animals. Here, we challenge the bilaterian origin hypothesis by combining large-scale receptor deorphanisation with phylogenetic analyses to identify monoamine receptors from the placozoan Trichoplax adhaerens. We demonstrate that these receptors are homologous to known bilaterian GPCRs, and behavioural assays demonstrate that monoamines like tyramine and tryptamine affect the speed of locomotion and body shape of this animal, respectively. These responses, together with the presence of biosynthetic enzymes for these molecules, reveal that monoaminergic signalling is both active and endogenous in placozoans. Our findings provide compelling evidence for a prebilaterian origin of monoaminergic systems, reshaping our understanding of early nervous system evolution. ### Competing Interest Statement The authors have declared no competing interest.

biorxiv.org

New preprint from the Senatore lab! Ancestral origin of the NALCN/Cch1 channelosome! Happy to have contributed! www.biorxiv.org/content/10.1...

NALCN/Cch1 channelosome subunits originated in early eukaryotes and are fully conserved in animals, fungi, and apusomonads

The sodium leak channel NALCN, a key regulator of neuronal excitability, associates with three ancillary subunits that are critical for its function: an extracellular subunit called FAM155, and two cytoplasmic subunits called UNC79 and UNC80. Interestingly, NALCN and FAM155 have orthologous phylogenetic relationships with the fungal calcium channel Cch1 and its extracellular subunit Mid1, however, UNC79 and UNC80 have not been reported outside of animals. In this study, we leveraged expanded gene sequence data available for eukaryotes to re-examine the evolutionary origins of NALCN and Cch1 channel subunits. Our analysis corroborates the direct phylogenetic relationship between NALCN and Cch1 and identifies a larger clade of related channels in additional eukaryotic taxa. We also identify homologues of FAM155/Mid1 in Cryptista algae, and UNC79 and UNC80 homologues in numerous non-metazoan eukaryotes including basidiomycete and mucoromycete fungi, and the microbial eukaryotic taxa Apusomonadida, Malawimonadida, and Discoba. Furthermore, we find that most major animal lineages, except ctenophores, possess a full complement of NALCN subunits. Comparing structural predictions with the solved structure of the human NALCN complex supports orthologous relationships between metazoan and non-metazoan FAM155/Mid1, UNC79, and UNC80 homologues. Together, our analyses reveal unexpected diversity and ancient eukaryotic origins of NALCN/Cch1 channelosome subunits and raise interesting questions about the functional nature of this conserved channel complex within a broad, eukaryotic context. ### Competing Interest Statement The authors have declared no competing interest.

biorxiv.org