Evidence map›Paper›PMID 24403603›Full record

ArticleMolecular biology of the cell2014

A microscopy-based screen employing multiplex genome sequencing identifies cargo-specific requirements for dynein velocity.

Kaeling Tan, Anthony J Roberts, Mark Chonofsky, Martin J Egan, Samara L Reck-Peterson

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Nuclear movement in fungi.Seminars in cell & developmental biology · 2018
    Review
  10. Article
  11. Article
  12. Article
  13. Cytoplasmic dynein and early endosome transport.Cellular and molecular life sciences : CMLS · 2015
    Review
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Kaeling TanDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115 Astbury Centre for Structural Molecular Biology, Faculty of Biological Sciences, School of Molecular and Cellular Biology, University of Leeds, Leeds LS2 9JT, United Kingdom.
Anthony J Roberts
Mark Chonofsky
Martin J Egan
Samara L Reck-Peterson
Harvard University · USUniversity of Leeds · GB

Funding

Cellular Control of Microtubule-Based Transport: Unraveling its Molecular MechanDP2OD004268 · OD · HARVARD MEDICAL SCHOOL · PI RECK-PETERSON, SAMARA L · 2008 to 2008
$2.5M
Dissecting dynein motor function using DNA nanotechnologyR01GM100947 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RECK-PETERSON, SAMARA L · 2013 to 2016
$1.2M
NIGMS NIH HHS R01 GM100947NIH HHS DP2 OD004268NIH HHS OD004268Wellcome Trust 092436/Z/10/Z
6 · The paper itself

Abstract

The timely delivery of membranous organelles and macromolecules to specific locations within the majority of eukaryotic cells depends on microtubule-based transport. Here we describe a screening method to identify mutations that have a critical effect on intracellular transport and its regulation using mutagenesis, multicolor-fluorescence microscopy, and multiplex genome sequencing. This screen exploits the filamentous fungus Aspergillus nidulans, which has many of the advantages of yeast molecular genetics but uses long-range microtubule-based transport in a manner more similar to metazoan cells. Using this method, we identified seven mutants that represent novel alleles of components of the intracellular transport machinery: specifically, kinesin-1, cytoplasmic dynein, and the dynein regulators Lis1 and dynactin. The two dynein mutations identified in our screen map to dynein's AAA+ catalytic core. Single-molecule studies reveal that both mutations reduce dynein's velocity in vitro. In vivo these mutants severely impair the distribution and velocity of endosomes, a known dynein cargo. In contrast, another dynein cargo, the nucleus, is positioned normally in these mutants. These results reveal that different dynein functions have distinct stringencies for motor performance.

Indexed as

Biological TransportAspergillus nidulansCytoplasmic DyneinsDynactin ComplexDyneinsFungal ProteinsHydro-LyasesKinesinsMicrotubule-Associated ProteinsMicrotubulesOrganellesPeroxisomesTemperatureArp1 protein, Aspergillus fumagatusCytoplasmic DyneinsDynactin ComplexDyneinsFungal ProteinsHydro-LyasesKinesinsMicrotubule-Associated Proteins

Identifiers

PMID24403603
PMCPMC3937092
OpenAlexW2098127198

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.