Regulated HsSAS-6 levels ensure formation of a single procentriole per centriole during the centrosome duplication cycle - Wikidata - wikimedia - TriplyDB

Regulated HsSAS-6 levels ensure formation of a single procentriole per centriole during the centrosome duplication cycle

Regulated HsSAS-6 levels ensure formation of a single procentriole per centriole during the centrosome duplication cycle

http://www.wikidata.org/entity/Q24647101

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Centrosome dysfunction contributes to chromosome instability, chromoanagenesis, and genome reprograming in cancer Centriole assembly and the role of Mps1: defensible or dispensable?Origin of the cell nucleus, mitosis and sex: roles of intracellular coevolution Basal body stability and ciliogenesis requires the conserved component Poc1 The human microcephaly protein STIL interacts with CPAP and is required for procentriole formation The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation.Stabilization of cartwheel-less centrioles for duplication requires CEP295-mediated centriole-to-centrosome conversion Ofd1, a human disease gene, regulates the length and distal structure of centrioles Centrobin-tubulin interaction is required for centriole elongation and stability RBM14 prevents assembly of centriolar protein complexes and maintains mitotic spindle integrity The SCF-FBXW5 E3-ubiquitin ligase is regulated by PLK4 and targets HsSAS-6 to control centrosome duplication Cep76, a centrosomal protein that specifically restrains centriole reduplication Ab ovo or de novo? Mechanisms of centriole duplication When 2+2=5: the origins and fates of aneuploid and tetraploid cells Production of Basal Bodies in bulk for dense multicilia formation p53 protects against genome instability following centriole duplication failure SAS-1 is a C2 domain protein critical for centriole integrity in C. elegans Structures of SAS-6 suggest its organization in centrioles Structural Basis of the 9-Fold Symmetry of Centrioles Structure of the SAS-6 cartwheel hub from Leishmania major SAS-6 engineering reveals interdependence between cartwheel and microtubules in determining centriole architecture The PLK4-STIL-SAS-6 module at the core of centriole duplication Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication Nek2 activation of Kif24 ensures cilium disassembly during the cell cycle The Cep63 paralogue Deup1 enables massive de novo centriole biogenesis for vertebrate multiciliogenesis Zika virus causes supernumerary foci with centriolar proteins and impaired spindle positioning Defective nucleotide excision repair with normal centrosome structures and functions in the absence of all vertebrate centrins SAS-4 is recruited to a dynamic structure in newly forming centrioles that is stabilized by the gamma-tubulin-mediated addition of centriolar microtubules.A multicomponent assembly pathway contributes to the formation of acentrosomal microtubule arrays in interphase Drosophila cells.Polo kinase and separase regulate the mitotic licensing of centriole duplication in human cells.Control of mitotic and meiotic centriole duplication by the Plk4-related kinase ZYG-1 Self-assembling SAS-6 multimer is a core centriole building block Procentriole assembly revealed by cryo-electron tomography Overly long centrioles and defective cell division upon excess of the SAS-4-related protein CPAP.Site-specific basal body duplication in Chlamydomonas.Centriole maturation requires regulated Plk1 activity during two consecutive cell cycles.Centriolar satellite- and hMsd1/SSX2IP-dependent microtubule anchoring is critical for centriole assembly DNA replication licensing factor Cdc6 and Plk4 kinase antagonistically regulate centrosome duplication via Sas-6.Control of daughter centriole formation by the pericentriolar material.The Centrioles, Centrosomes, Basal Bodies, and Cilia of Drosophila melanogaster.

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Regulated HsSAS-6 levels ensure formation of a single procentriole per centriole during the centrosome duplication cycle

http://www.wikidata.org/entity/Q24647101

description

2007 nî lūn-bûn

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2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի օգոստոսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

@ast

Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

@en

Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

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type

label

Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

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Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

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Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

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prefLabel

Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

@ast

Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

@en

Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

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J.DEVCEL.2007.07.004

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Developmental Cell

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Regulated HsSAS-6 levels ensur ...... e centrosome duplication cycle

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Alexey Khodjakov

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Tatiana Vinogradova

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Ursula Euteneuer

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P2860

The Polo kinase Plk4 functions in centriole duplication

Centrin-2 is required for centriole duplication in mammalian cells

C-Nap1, a novel centrosomal coiled-coil protein and candidate substrate of the cell cycle-regulated protein kinase Nek2

SAS-6 defines a protein family required for centrosome duplication in C. elegans and in human cells

Nonperiodic activity of the human anaphase-promoting complex-Cdh1 ubiquitin ligase results in continuous DNA synthesis uncoupled from mitosis

The KEN box: an APC recognition signal distinct from the D box targeted by Cdh1

The de novo centriole assembly pathway in HeLa cells: cell cycle progression and centriole assembly/maturation

Centriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis

Centriole cycle in Chinese hamster ovary cells as determined by whole-mount electron microscopy

Centrioles in the cell cycle. I. Epithelial cells

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203-213

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10.1016/J.DEVCEL.2007.07.004

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Sebastian A. Leidel

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6158618

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2628752

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