Distinct mechanoreceptor pezo-1 isoforms modulate food intake in the nematode Caenorhabditis elegans

Two PIEZO mechanosensitive cation channels, PIEZO1 and PIEZO2, have been identified in mammals, where they are involved in numerous sensory processes. While structurally similar, PIEZO channels are expressed in distinct tissues and exhibit unique properties. How different PIEZOs transduce force, how their transduction mechanism varies, and how their unique properties match the functional needs of the tissues they are expressed in remain all-important unanswered questions. The nematode Caenorhabditis elegans has a single PIEZO ortholog (pezo-1) predicted to have 12 isoforms. These isoforms share many transmembrane domains but differ in those that distinguish PIEZO1 and PIEZO2 in mammals. We used transcriptional and translational reporters to show that putative promoter sequences immediately upstream of the start codon of long pezo-1 isoforms predominantly drive green fluorescent protein (GFP) expression in mesodermally derived tissues (such as muscle and glands). In contrast, sequences upstream of shorter pezo-1 isoforms resulted in GFP expression primarily in neurons. Putative promoters upstream of different isoforms drove GFP expression in different cells of the same organs of the digestive system. The observed unique pattern of complementary expression suggests that different isoforms could possess distinct functions within these organs. We used mutant analysis to show that pharyngeal muscles and glands require long pezo-1 isoforms to respond appropriately to the presence of food. The number of pezo-1 isoforms in C. elegans, their putative differential pattern of expression, and roles in experimentally tractable processes make this an attractive system to investigate the molecular basis for functional differences between members of the PIEZO family of mechanoreceptors.Fil: Hughes, Kiley. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Shah, Ashka. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Bai, Xiaofei. National Institutes of Health; Estados UnidosFil: Adams, Jessica. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Bauer, Rosemary. University of Chicago; Estados UnidosFil: Jackson, Janelle. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Harris, Emily. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Ficca, Alyson. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Freebairn, Ploy. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Mohammed, Shawn. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Fernandez, Eliana Mailen. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Bainbridge, Chance. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Brocco, Marcela Adriana. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas. - Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Stein, Wolfgang. University Of Illinois. Deparment Of Biological Science; Estados UnidosFil: Vidal Gadea, Andrés G.. University Of Illinois. Deparment Of Biological Science; Estados Unido

Extended Data Video: Sample movie of eight unc-31(e928) mutants swimming in liquid nematode growth media.

Sample movie of eight unc-31(e928) mutants swimming in liquid nematode growth media like the ones used to illustrate the functionality of the tracking system. Movies were saved as avi and later imported and processed in ImageJ. The different steps of pre-processing are illustrated as is the result of the tracking analysis.Related Publication: Affordable Caenorhabditis elegans tracking system for classroom use Nicholas Leonard Normal University High School, Normal, Illinois Andrés G. Vidal-Gadea School of Biological Sciences, Illinois State University, Normal, Illinois microPublication Biology 2021-03-17 https://doi.org/10.17912/micropub.biology.000377 engContact person: Andrés G. Vidal-Gadea [email protected]

Extended Data Figure: Stencil for the construction of the affordable worm tracker.

Stencil for the construction of the affordable worm tracker. The stencil should be printed in an 8x11in standard page and used as a guide in the construction of the tracker. Refer to the text for instructions.Related Publication: Affordable Caenorhabditis elegans tracking system for classroom use Nicholas Leonard Normal University High School, Normal, Illinois Andrés G. Vidal-Gadea School of Biological Sciences, Illinois State University, Normal, Illinois microPublication Biology 2021-03-17 https://doi.org/10.17912/micropub.biology.000377 engContact person: Andrés G. Vidal-Gadea [email protected]

Neuronal membrane glycoprotein (nmgp-1) gene deficiency affects chemosensation-related behaviors, dauer exit and egg-laying in Caenorhabditis elegans

The nervous system monitors the environment to maintain homeostasis, which can be affected by stressful conditions. Using mammalian models of chronic stress, we previously observed altered brain levels of GPM6A, a protein involved in neuronal morphology. However, GPM6A's role in systemic stress responses remains unresolved. The nematode Caenorhabditis elegans expresses a GPM6A ortholog, the neuronal membrane glycoprotein 1 (NMGP-1). Because of the shared features between nematode and mammalian nervous systems and the vast genetic tools available in C. elegans, we used the worm to elucidate the role of GPM6A in the stress response. We first identified nmgp-1 expression in different amphid and phasmid neurons. To understand the nmgp-1 role, we characterized the behavior of nmgp-1(RNAi) animals and two nmgp-1 mutant alleles. Compared to control animals, mutant and RNAi-treated worms exhibited increased recovery time from the stress-resistant dauer stage, altered SDS chemosensation and reduced egg-laying rate resulting in egg retention (bag-of-worms phenotype). Silencing of nmgp-1 expression induced morphological abnormalities in the ASJ sensory neurons, partly responsible for dauer exit. These results indicate that nmgp-1 is required for neuronal morphology and for behaviors associated with chemosensation. Finally, we propose nmgp-1 mutants as a tool to screen drugs for human nervous system pathologies.Fil: Fernandez, Eliana Mailen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Cutraro, Yamila B.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Adams, Jessica. Illinois State University; Estados UnidosFil: Monteleone, Melisa Carolina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Hughes, Kiley J.. Illinois State University; Estados UnidosFil: Frasch, Alberto Carlos C.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; ArgentinaFil: Vidal Gadea, Andrés G.. Illinois State University; Estados UnidosFil: Brocco, Marcela Adriana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; Argentin

Lifetime measurements in Ti 52,54 to study shell evolution toward N=32

AGATA CollaborationLifetimes of the excited states in the neutron-rich Ti52,54 nuclei, produced in a multinucleon-transfer reaction, were measured by employing the Cologne plunger device and the recoil-distance Doppler-shift method. The experiment was performed at the Grand Accélérateur National d'Ions Lourds facility by using the Advanced Gamma Tracking Array for the γ-ray detection, coupled to the large-acceptance variable mode spectrometer for an event-by-event particle identification. A comparison between the transition probabilities obtained from the measured lifetimes of the 21+ to 81+ yrast states in Ti52,54 and that from the shell-model calculations based on the well-established GXPF1A, GXPF1B, and KB3G fp shell interactions support the N=32 subshell closure. The B(E2) values for Ti52 determined in this work are in disagreement with the known data, but are consistent with the predictions of the shell-model calculations and reduce the previously observed pronounced staggering across the even-even titanium isotopes

Development of a citrus genome-wide EST collection and cDNA microarray as resources for genomic studies

A functional genomics project has been initiated to approach the molecular characterization of the main biological and agronomical traits of citrus. As a key part of this project, a citrus EST collection has been generated from 25 cDNA libraries covering different tissues, developmental stages and stress conditions. The collection includes a total of 22,635 high-quality ESTs, grouped in 11,836 putative unigenes, which represent at least one third of the estimated number of genes in the citrus genome. Functional annotation of unigenes which have Arabidopsis orthologues (68% of all unigenes) revealed gene representation in every major functional category, suggesting that a genome-wide EST collection was obtained. A Citrus clementina Hort. ex Tan. cv. Clemenules genomic library, that will contribute to further characterization of relevant genes, has also been constructed. To initiate the analysis of citrus transcriptome, we have developed a cDNA microarray containing 12,672 probes corresponding to 6875 putative unigenes of the collection. Technical characterization of the microarray showed high intra- and inter-array reproducibility, as well as a good range of sensitivity. We have also validated gene expression data achieved with this microarray through an independent technique such as RNA gel blot analysis