Literature DB >> 35800466

Quantitative Analysis of Actin Cable Length in Yeast.

Shane G McInally1,2, Jane Kondev2, Bruce L Goode1.   

Abstract

Polarized actin cables in S. cerevisiae are linear bundles of crosslinked actin filaments that are assembled by two formins, Bnr1 (localized to the bud neck), and Bni1 (localized to the bud tip). Actin is polymerized at these two sites, which results in cables extending along the cell cortex toward the back of the mother cell. These cables serve as polarized tracks for myosin-based transport of secretory vesicles and other cargo, from the mother cell to the growing daughter cell. Until recently, descriptions of actin cable morphology and architecture have largely been qualitative or descriptive in nature. Here, we introduce a new quantitative method that enables more precise characterization of actin cable length. This technological advance generates quantitative datasets that can be used to determine the contributions of different actin regulatory proteins to the maintenance of cable architecture, and to assess how different pharmacological agents affect cable arrays. Additionally, these datasets can be used to test theoretical models, and be compared to results from computational simulations of actin assembly. Graphical abstract: Illustration of actin cable length and morphology analysis. (A) Representative maximum intensity projection image of S. cerevisiae fixed and stained with fluorescently-conjugated phalloidin to label F-actin (displayed in color), and fluorescently-conjugated Concanavalin A to label the cell wall (displayed in grey scale). Lengths of actin cables traced from the bud neck to their ends are indicated (dashed lines). (B) Inverted grey scale image of F-actin labelled with fluorescently-conjugated phalloidin and the cell wall traced in black. The length (purple) and end-to-end distance (green) of a single actin cable is indicated. Scale bar, 2 µm. (C-E) Actin cable length (C), end-to-end distance (D), and tortuosity (E) from hypothetical datasets, where each data point represents an individual cable and larger symbols represent the mean from each hypothetical experiment. Error bars, 95% confidence intervals.
Copyright © The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Actin cable; Budding yeast; Cytoskeleton; Formin; Microscopy; S. cerevisiae

Year:  2022        PMID: 35800466      PMCID: PMC9090523          DOI: 10.21769/BioProtoc.4402

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  7 in total

1.  Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast.

Authors:  David Pruyne; Lina Gao; Erfei Bi; Anthony Bretscher
Journal:  Mol Biol Cell       Date:  2004-09-15       Impact factor: 4.138

2.  Fluorescent Labeling of Yeast Cell Wall Components.

Authors:  Hiroki Okada; Yoshikazu Ohya
Journal:  Cold Spring Harb Protoc       Date:  2016-08-01

Review 3.  The yeast actin cytoskeleton: from cellular function to biochemical mechanism.

Authors:  James B Moseley; Bruce L Goode
Journal:  Microbiol Mol Biol Rev       Date:  2006-09       Impact factor: 11.056

Review 4.  Design Principles of Length Control of Cytoskeletal Structures.

Authors:  Lishibanya Mohapatra; Bruce L Goode; Predrag Jelenkovic; Rob Phillips; Jane Kondev
Journal:  Annu Rev Biophys       Date:  2016-04-29       Impact factor: 12.981

5.  SuperPlots: Communicating reproducibility and variability in cell biology.

Authors:  Samuel J Lord; Katrina B Velle; R Dyche Mullins; Lillian K Fritz-Laylin
Journal:  J Cell Biol       Date:  2020-06-01       Impact factor: 10.539

6.  Common formin-regulating sequences in Smy1 and Bud14 are required for the control of actin cable assembly in vivo.

Authors:  Julian A Eskin; Aneliya Rankova; Adam B Johnston; Salvatore L Alioto; Bruce L Goode
Journal:  Mol Biol Cell       Date:  2016-01-13       Impact factor: 4.138

7.  Scaling of subcellular actin structures with cell length through decelerated growth.

Authors:  Shane G McInally; Jane Kondev; Bruce L Goode
Journal:  Elife       Date:  2021-06-11       Impact factor: 8.140

  7 in total

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