Detail of Worm_lethargus

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Project
Title
Time-lapse images of C. elegans lethargus dynamics of four different genotypes by rapid C. elegans motion imaging (Remi) system
Description
To observe the duration of lethargus of C. elegans, each mutant was simultaneously imaged every 2 sec for 14 hours by rapid C. elegans motion imaging (Remi) system;the wild type (1st and 2nd rows from the left), pek-1 mutant (3rd and 4th rows), sel-11 mutant (5th and 6th rows), and double mutants of pek-1 and sel-11 (7th and 8th rows).
Release, Updated
2024-11-25
License
CC-BY
Kind
Image data
File Formats
.jpg
Data size
3.6 GB

Organism
Caenorhabditis elegans  ( NCBITaxon:6239 )
Strain(s)
N2, SLP544, SLP266, SLP808
Cell Line
-

Datatype
-
Molecular Function (MF)
Biological Process (BP)
sleep ( GO:0030431 )
Cellular Component (CC)
Biological Imaging Method
time lapse microscopy ( Fbbi:00000249 )
rapid C. elegans motion imaging (Remi) system
X scale
15 micrometer/pixel
Y scale
15 micrometer/pixel
Z scale
-
T scale
2 seconds per time interval

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
See details in Kawano T, et. al. Cell Rep. 2023 Mar 28;42(3):112267
Related paper(s)

Taizo Kawano, Mitsuaki Kashiwagi, Mika Kanuka, Chung-Kuan Chen, Shinnosuke Yasugaki, Sena Hatori, Shinichi Miyazaki, Kaeko Tanaka, Hidetoshi Fujita, Toshiro Nakajima, Masashi Yanagisawa, Yoshimi Nakagawa, Yu Hayashi (2023) ER proteostasis regulators cell-non-autonomously control sleep., Cell reports, Volume 42, Number 3, pp. 112267

Published in 2023 Mar 15 (Electronic publication in March 15, 2023, midnight )

(Abstract) Sleep is regulated by peripheral tissues under fatigue. The molecular pathways in peripheral cells that trigger systemic sleep-related signals, however, are unclear. Here, a forward genetic screen in C. elegans identifies 3 genes that strongly affect sleep amount: sel-1, sel-11, and mars-1. sel-1 and sel-11 encode endoplasmic reticulum (ER)-associated degradation components, whereas mars-1 encodes methionyl-tRNA synthetase. We find that these machineries function in non-neuronal tissues and that the ER unfolded protein response components inositol-requiring enzyme 1 (IRE1)/XBP1 and protein kinase R-like ER kinase (PERK)/eukaryotic initiation factor-2alpha (eIF2alpha)/activating transcription factor-4 (ATF4) participate in non-neuronal sleep regulation, partly by reducing global translation. Neuronal epidermal growth factor receptor (EGFR) signaling is also required. Mouse studies suggest that this mechanism is conserved in mammals. Considering that prolonged wakefulness increases ER proteostasis stress in peripheral tissues, our results suggest that peripheral ER proteostasis factors control sleep homeostasis. Moreover, based on our results, peripheral tissues likely cope with ER stress not only by the well-established cell-autonomous mechanisms but also by promoting the individual's sleep.

Contact
Yu Hayashi , University of Tsukuba , International Institute for Integrative Sleep Medicine (WPI-IIIS)
Contributors
Taizo Kawano

OMERO Dataset
OMERO Project
Source