RRC ID 59375
Author Liu X, Guo X, Niu L, Li X, Sun F, Hu J, Wang X, Shen K.
Title Atlastin-1 regulates morphology and function of endoplasmic reticulum in dendrites.
Journal Nat Commun
Abstract Endoplasmic reticulum (ER) is characterized by interconnected tubules and sheets. Neuronal ER adopts specific morphology in axons, dendrites and soma. Here we study mechanisms underlying ER morphogenesis in a C. elegans sensory neuron PVD. In PVD soma and dendrite branch points, ER tubules connect to form networks. ER tubules fill primary dendrites but only extend to some but not all dendritic branches. We find that the Atlastin-1 ortholog, atln-1 is required for neuronal ER morphology. In atln-1 mutants with impaired GTPase activity, ER networks in soma and dendrite branch points are reduced and replaced by tubules, and ER tubules retracted from high-order dendritic branches, causing destabilized microtubule in these branches. The abnormal ER morphology likely causes defects in mitochondria fission at dendritic branch points. Mutant alleles of Atlastin-1 found in Hereditary Spastic Paraplegia (HSP) patients show similar ER phenotypes, suggesting that neuronal ER impairment contributes to HSP disease pathogenesis.
Volume 10(1)
Pages 568
Published 2019-2-4
DOI 10.1038/s41467-019-08478-6
PII 10.1038/s41467-019-08478-6
PMID 30718476
PMC PMC6362286
MeSH Animals Caenorhabditis elegans / genetics Caenorhabditis elegans / metabolism* Caenorhabditis elegans Proteins / genetics Caenorhabditis elegans Proteins / metabolism* Dendrites / genetics Dendrites / metabolism* Endoplasmic Reticulum / genetics Endoplasmic Reticulum / metabolism* GTP-Binding Proteins / genetics GTP-Binding Proteins / metabolism Membrane Proteins / genetics Membrane Proteins / metabolism Microtubules / metabolism Spastic Paraplegia, Hereditary / genetics Spastic Paraplegia, Hereditary / metabolism
IF 11.878
Times Cited 5
Resource
C.elegans tm3667 tm683 tm390