Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast
about
The yeast actin cytoskeleton: from cellular function to biochemical mechanismMultifunctional Microtubule-Associated Proteins in PlantsThe final cut: cell polarity meets cytokinesis at the bud neck in S. cerevisiaeActomyosin ring driven cytokinesis in budding yeastAnd the dead shall rise: actin and myosin return to the spindleCommon formin-regulating sequences in Smy1 and Bud14 are required for the control of actin cable assembly in vivo.The Stationary-Phase Cells of Saccharomyces cerevisiae Display Dynamic Actin Filaments Required for Processes Extending Chronological Life Span.Actin-mediated delivery of astral microtubules instructs Kar9p asymmetric loading to the bud-ward spindle pole.Requirement for the polarisome and formin function in Ssk2p-mediated actin recovery from osmotic stress in Saccharomyces cerevisiae.Cdc42p regulation of the yeast formin Bni1p mediated by the effector Gic2p.Fertility and polarized cell growth depends on eIF5A for translation of polyproline-rich formins in Saccharomyces cerevisiae.Displacement of formins from growing barbed ends by bud14 is critical for actin cable architecture and function.Plasma membrane aminoglycerolipid flippase function is required for signaling competence in the yeast mating pheromone response pathwayRegulation of cell polarity by interactions of Msb3 and Msb4 with Cdc42 and polarisome components.Requirements of Slm proteins for proper eisosome organization, endocytic trafficking and recycling in the yeast Saccharomyces cerevisiae.Saccharomyces cerevisiae Kelch proteins and Bud14 protein form a stable 520-kDa formin regulatory complex that controls actin cable assembly and cell morphogenesisAssembly of the PtdIns 4-kinase Stt4 complex at the plasma membrane requires Ypp1 and Efr3.Role of a Cdc42p effector pathway in recruitment of the yeast septins to the presumptive bud site.Differential activities and regulation of Saccharomyces cerevisiae formin proteins Bni1 and Bnr1 by Bud6.The septins function in G1 pathways that influence the pattern of cell growth in budding yeast.Homologues of oxysterol-binding proteins affect Cdc42p- and Rho1p-mediated cell polarization in Saccharomyces cerevisiae.Ligand-induced activation of a formin-NPF pair leads to collaborative actin nucleationThe pleckstrin homology domain proteins Slm1 and Slm2 are required for actin cytoskeleton organization in yeast and bind phosphatidylinositol-4,5-bisphosphate and TORC2.Control of Formin Distribution and Actin Cable Assembly by the E3 Ubiquitin Ligases Dma1 and Dma2.Existence of a novel clathrin-independent endocytic pathway in yeast that depends on Rho1 and formin.Initial polarized bud growth by endocytic recycling in the absence of actin cable-dependent vesicle transport in yeast.From function to shape: a novel role of a formin in morphogenesis of the fungus Ashbya gossypii.Yeast formins Bni1 and Bnr1 utilize different modes of cortical interaction during the assembly of actin cables.mRNAs encoding polarity and exocytosis factors are cotransported with the cortical endoplasmic reticulum to the incipient bud in Saccharomyces cerevisiae.Endocytosis optimizes the dynamic localization of membrane proteins that regulate cortical polarity.Polarized growth in budding yeast in the absence of a localized formin.The myosin passenger protein Smy1 controls actin cable structure and dynamics by acting as a formin damperImmobile myosin-II plays a scaffolding role during cytokinesis in budding yeast.The formins Cdc12 and For3 cooperate during contractile ring assembly in cytokinesis.Myosin‑II heavy chain and formin mediate the targeting of myosin essential light chain to the division site before and during cytokinesis.Analysis of unregulated formin activity reveals how yeast can balance F-actin assembly between different microfilament-based organizations.Intrinsic capability of budding yeast cofilin to promote turnover of tropomyosin-bound actin filaments.A septin from the filamentous fungus A. nidulans induces atypical pseudohyphae in the budding yeast S. cerevisiaeFormins in development: orchestrating body plan origami.Changes in Bni4 localization induced by cell stress in Saccharomyces cerevisiae.
P2860
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P2860
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast
description
2004 nî lūn-bûn
@nan
2004 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast
@ast
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast
@en
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast.
@nl
type
label
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast
@ast
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast
@en
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast.
@nl
prefLabel
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast
@ast
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast
@en
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast.
@nl
P2093
P2860
P3181
P356
P1476
Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast
@en
P2093
Anthony Bretscher
David Pruyne
P2860
P304
P3181
P356
10.1091/MBC.E04-04-0296
P407
P577
2004-09-15T00:00:00Z