With Age Comes Maturity: Biochemical and Structural Transformation of a Human Centriole in the Making.

centriole duplication centriole elongation centriole maturation centrosome

Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
09 06 2020
Historique:
received: 12 05 2020
revised: 29 05 2020
accepted: 04 06 2020
entrez: 13 6 2020
pubmed: 13 6 2020
medline: 19 3 2021
Statut: epublish

Résumé

Centrioles are microtubule-based cellular structures present in most human cells that build centrosomes and cilia. Proliferating cells have only two centrosomes and this number is stringently maintained through the temporally and spatially controlled processes of centriole assembly and segregation. The assembly of new centrioles begins in early S phase and ends in the third G1 phase from their initiation. This lengthy process of centriole assembly from their initiation to their maturation is characterized by numerous structural and still poorly understood biochemical changes, which occur in synchrony with the progression of cells through three consecutive cell cycles. As a result, proliferating cells contain three structurally, biochemically, and functionally distinct types of centrioles: procentrioles, daughter centrioles, and mother centrioles. This age difference is critical for proper centrosome and cilia function. Here we discuss the centriole assembly process as it occurs in somatic cycling human cells with a focus on the structural, biochemical, and functional characteristics of centrioles of different ages.

Identifiants

pubmed: 32526902
pii: cells9061429
doi: 10.3390/cells9061429
pmc: PMC7349492
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Intramural Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Catherine Sullenberger (C)

Laboratory of Protein Dynamics and Signaling, NIH/NCI/CCR, Frederick, MD 21702, USA.

Alejandra Vasquez-Limeta (A)

Laboratory of Protein Dynamics and Signaling, NIH/NCI/CCR, Frederick, MD 21702, USA.

Dong Kong (D)

Laboratory of Protein Dynamics and Signaling, NIH/NCI/CCR, Frederick, MD 21702, USA.

Jadranka Loncarek (J)

Laboratory of Protein Dynamics and Signaling, NIH/NCI/CCR, Frederick, MD 21702, USA.

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Classifications MeSH