High-resolution characterization of centriole distal appendage morphology and dynamics by correlative STORM and electron microscopy.
Animals
Aurora Kinase A
CRISPR-Cas Systems
Cell Cycle Proteins
/ ultrastructure
Centrioles
/ ultrastructure
Cilia
/ ultrastructure
DNA-Binding Proteins
Electron Microscope Tomography
/ methods
HeLa Cells
Humans
Intercellular Signaling Peptides and Proteins
Mice
Mice, Inbred C57BL
Microscopy, Electron
/ methods
Microtubule Proteins
/ ultrastructure
Microtubules
/ ultrastructure
Mitosis
Protein Serine-Threonine Kinases
Proto-Oncogene Proteins
Species Specificity
Transcription Factors
Polo-Like Kinase 1
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
01 03 2019
01 03 2019
Historique:
received:
16
07
2018
accepted:
10
12
2018
entrez:
3
3
2019
pubmed:
3
3
2019
medline:
5
4
2019
Statut:
epublish
Résumé
Centrioles are vital cellular structures that form centrosomes and cilia. The formation and function of cilia depends on a set of centriole's distal appendages. In this study, we use correlative super resolution and electron microscopy to precisely determine where distal appendage proteins localize in relation to the centriole microtubules and appendage electron densities. Here we characterize a novel distal appendage protein ANKRD26 and detail, in high resolution, the initial steps of distal appendage assembly. We further show that distal appendages undergo a dramatic ultra-structural reorganization before mitosis, during which they temporarily lose outer components, while inner components maintain a nine-fold organization. Finally, using electron tomography we reveal that mammalian distal appendages associate with two centriole microtubule triplets via an elaborate filamentous base and that they appear as almost radial finger-like protrusions. Our findings challenge the traditional portrayal of mammalian distal appendage as a pinwheel-like structure that is maintained throughout mitosis.
Identifiants
pubmed: 30824690
doi: 10.1038/s41467-018-08216-4
pii: 10.1038/s41467-018-08216-4
pmc: PMC6397210
doi:
Substances chimiques
Ankrd26 protein, mouse
0
Cell Cycle Proteins
0
DNA-Binding Proteins
0
Intercellular Signaling Peptides and Proteins
0
Microtubule Proteins
0
Proto-Oncogene Proteins
0
Transcription Factors
0
Aurora Kinase A
EC 2.7.11.1
Protein Serine-Threonine Kinases
EC 2.7.11.1
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, N.I.H., Intramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
993Subventions
Organisme : NIDDK NIH HHS
ID : R01 DK108005
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM101026
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM114119
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL128370
Pays : United States
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