Subcellular Localization of ESCRT-II in the Nematode C. elegans by Correlative Light Electron Microscopy

2019 ◽  
pp. 49-61
Author(s):  
Céline Largeau ◽  
Emmanuel Culetto ◽  
Renaud Legouis
Keyword(s):  
Electron Microscopy ◽  
Subcellular Localization ◽  
C Elegans

scholarly journals Centriolar remodeling underlies basal body maturation during ciliogenesis in Caenorhabditis elegans

eLife ◽  
2017 ◽  
Vol 6 ◽  
Author(s):  
Inna V Nechipurenko ◽  
Cristina Berciu ◽  
Piali Sengupta ◽  
Daniela Nicastro
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Sensory Neurons ◽  
Basal Body ◽  
Three Dimensional ◽  
C Elegans ◽  
Mother Centriole ◽  
Section Electron ◽  
Serial Section Electron Microscopy ◽  
Section Electron Microscopy

The primary cilium is nucleated by the mother centriole-derived basal body (BB) via as yet poorly characterized mechanisms. BBs have been reported to degenerate following ciliogenesis in the C. elegans embryo, although neither BB architecture nor early ciliogenesis steps have been described in this organism. In a previous study (Doroquez et al., 2014), we described the three-dimensional morphologies of sensory neuron cilia in adult C. elegans hermaphrodites at high resolution. Here, we use serial section electron microscopy and tomography of staged C. elegans embryos to demonstrate that BBs remodel to support ciliogenesis in a subset of sensory neurons. We show that centriolar singlet microtubules are converted into BB doublets which subsequently grow asynchronously to template the ciliary axoneme, visualize degeneration of the centriole core, and define the developmental stage at which the transition zone is established. Our work provides a framework for future investigations into the mechanisms underlying BB remodeling.

scholarly journals Combinatorial Expression of TRPV Channel Proteins Defines Their Sensory Functions and Subcellular Localization in C. elegans Neurons

Neuron ◽  
2002 ◽  
Vol 35 (2) ◽  
pp. 307-318 ◽  
Author(s):  
David M. Tobin ◽  
David M. Madsen ◽  
Amanda Kahn-Kirby ◽  
Erin L. Peckol ◽  
Gary Moulder ◽  
...  
Keyword(s):  
Subcellular Localization ◽  
C Elegans ◽  
Channel Proteins ◽  
Sensory Functions ◽  
Combinatorial Expression

scholarly journals Neuroendocrine Modulation Sustains the C. elegans Forward Motor State

2016 ◽  
Author(s):  
Maria A. Lim ◽  
Jyothsna Chitturi ◽  
Valeriya Laskova ◽  
Jun Meng ◽  
Daniel Findeis ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Calcium Imaging ◽  
Neural Circuit ◽  
Transcriptome Profiling ◽  
Behavioral State ◽  
Forward Movement ◽  
C Elegans ◽  
Peptidergic Neuron ◽  
Homeobox Transcription Factor

AbstractNeuromodulators shape neural circuit dynamics. Combining electron microscopy, genetics, transcriptome profiling, calcium imaging, and optogenetics, we discovered a peptidergic neuron that modulates C. elegans motor circuit dynamics. The Six/SO-family homeobox transcription factor UNC-39 governs lineage-specific neurogenesis to give rise to a neuron RID. RID bears the anatomic hallmarks of a specialized endocrine neuron: it harbors near-exclusive dense core vesicles that cluster periodically along the axon, and expresses multiple neuropeptides, including the FMRF-amide-related FLP-14. RID activity increases during forward movement. Ablating RID reduces the sustainability of forward movement, a phenotype partially recapitulated by removing FLP-14. Optogenetic depolarization of RID prolongs forward movement, an effect reduced in the absence of FLP-14. Together, these results establish the role of a neuroendocrine cell RID in sustaining a specific behavioral state in C. elegans.

scholarly journals Subcellular localization of the Triple Gene Block movement proteins of Beet necrotic yellow vein virus by electron microscopy

Virology ◽  
2005 ◽  
Vol 340 (1) ◽  
pp. 155-166 ◽  
Author(s):  
M. Erhardt ◽  
G. Vetter ◽  
D. Gilmer ◽  
S. Bouzoubaa ◽  
K. Richards ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Subcellular Localization ◽  
Triple Gene Block ◽  
Yellow Vein ◽  
Movement Proteins ◽  
Gene Block ◽  
Block Movement
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