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I am very happy to announce that our lab will soon move to the University of to join the Centre for Organismal Studies (COS)
cos.uni-heidelberg.de/en

1/5

Great paper by Laura Piovani on high-quality cell atlases of oyster and polyclad flatworm larvae. Interesting new insights into cell-type diversity, young and old cell-types and evolution. Shell gland transcriptomes make oyster larvae look young. It was a pleasure to collaborate with Telford Lab et al. on this project. biorxiv.org/content/10.1101/20

In this paper we generated most of the figures entirely in R for open science and reproducibility. All code is shared here:
github.com/JekelyLab/Jasek_et_
The figures and analyses can be regenerated by the code that will query our public database where all EM data, tracings and annotations are shared:
catmaid.jekelylab.ex.ac.uk (project id: 11)

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We also mapped synapses to the desmosomal connectome to infer the extent of tissue influenced by motoneurons. We suggest that such cellular-level maps based on data and the integrative analysis of synaptic and adherent force networks will be important to elucidate body mechanics and the nervous control of movement.

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The formed by the and supported by many muscles is quite unique to polychaete annelids and represents the only example outside the of animals with a trunk appendages rigidified by an endoskeleton. Aciculae evolved in stem errant in the Early indicating the deep ancestry of these structures, predating tetrapod limbs.

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We analysed the network in many different ways and found that its structure is quite different from the synaptic and random networks. One of the interesting findings was that the - chitin rods that form an in the segmental - are highly connected hubs in the and a large number of is involved in moving them.

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Sanja skeletonised all the 853 muscle cells in the larva and annotated their desmosomes and the partner cells and extracellular structures that the desmosomes attach to. This resulted in a single network of over 2,000 cells and extracellular structures (basal lamina, chitin endoskeleton etc) that we call the desmosomal . In synaptic connectomes the links are formed by , in a desmosomal connectome the links are desmosomes.

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New structure from LSI Exeter colleagues Matthew Gaines et al. Bertram Daum lab, this time of the enigmatic filament called 'thread'.

What I find cool about this work is that first they had the structure, then found the sequence based on glycosylation sites and bulky residues.
This was also so ultra-stable, that resisted trypsinisation, so mass spec was not an option to identify it.
ncbi.nlm.nih.gov/pmc/articles/

Our review with Stefan Gründer and Audrey Ortega Ramírez is out:

"Neuropeptides and DEG/ENaC ion channels: a relationship from mammals to cnidarians"

where we conclude based on structural comparisons and the of systems that the interaction of DEG/ENaC channels with neuropeptides has diverse structural bases and many origins.

doi.org/10.1113/JP282309

Finally, here is the Editor's evaluation from @elife

This paper reports on the development of an impressive microfluidic platform for the study of motility, and motility transitions, exhibited by single algal cells in circular confinement. Building on previous work that showed a three-state motility repertoire for certain green algae, the present work uses extremely long time series and a variety of physical perturbations to show how those dynamics can be altered by environmental conditions. The work will be of interest to a wide range of scientists studying motility and non-equilibrium dynamics.
doi.org/10.7554/eLife.76519.sa

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The authors also developed and tested a novel droplet-fusion assay to expose single cells in a controlled manner to chemicals. This could be a very elegant way to e.g., dissect mechanisms in the cells by .

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The motility is light-switchable, which was known, but the long-term imaging of single cells in light and dark revealed a cellular : the light-altered behavioural state persisted after light off.

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The locomotion of single-cells is characterised by a trio of motility macrostates (run, stop, tumble) with distinct transition probabilities that could be quantified by long-term imaging.

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(2 ) and (8 cilia) were encapsulated into droplets by and imaged at high speed to characterise gait switching dynamics and the effect of light.

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Great paper: a droplet assay to encapsulate single micron-sized algae to study long-term .
elifesciences.org/articles/765
by Bentley et al. gielenlab.com and @micromotility
A thread.

..and the , with some holes in it.
Now we would need a choanoflagellate ciliary .

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and the ciliary vane, which is very different from the mastigonemes of e..g.
A cilium with wings.

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here is a picture of the central pair, tomographic slices and averages

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Beautiful paper on choanoflagellate revealing the enigmatic ciliary vane, new components and similarities to animal cilia

elifesciences.org/articles/781

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