Evidence map›Paper›PMID 7622564›Full record

ArticleThe Journal of cell biology1995

Analysis of MAP 4 function in living cells using green fluorescent protein (GFP) chimeras.

K R Olson, J R McIntosh, J B Olmsted

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
8.1field-weighted citation impact, top 2% 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

61 citing papers in PubMed, 194 citations in OpenAlex.

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  6. Measuring microtubule dynamics.Essays in biochemistry · 2018
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  17. The role of microtubules and their dynamics in cell migration.The Journal of biological chemistry · 2012
    Article
  18. Article
  19. Article
  20. Article

1 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

K R OlsonDepartment of Biology, University of Rochester, New York 14627, USA.
J R McIntosh
J B Olmsted
University of Rochester · US

Funding

CELLULAR CONTROL OF NEURONAL CYTOSKELETON ASSEMBLYR01GM022214 · NIGMS · UNIVERSITY OF ROCHESTER · PI OLMSTED, JOANNA B · 1985 to 1995
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MITOTIC MOTORSR01GM036663 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI MCINTOSH, J RICHARD · 1986 to 1999
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NIGMS NIH HHS GM22214NIGMS NIH HHS GM36663
6 · The paper itself

Abstract

MAP 4 is a ubiquitous microtubule-associated protein thought to play a role in the polymerization and stability of microtubules in interphase and mitotic cells. We have analyzed the behavior of protein domains of MAP 4 in vivo using chimeras constructed from these polypeptides and the green fluorescent protein (GFP). GFP-MAP 4 localizes to microtubules; this is confirmed by colocalization of GFP-MAP 4 with microtubules that have incorporated microinjected rhodamine-tubulin, and by loss of localized fluorescence after treatment of cells with anti-microtubule agents. Different subdomains of MAP 4 have distinct effects on microtubule organization and dynamics. The entire basic domain of MAP 4 reorganizes microtubules into bundles and stabilizes these arrays against depolymerization with nocodazole. Within the basic domain, the PGGG repeats, which are conserved with MAP 2 and tau, have a weak affinity for microtubules and are dispensable for microtubule binding, whereas the MAP 4-unique PSP region can function independently in binding. The projection domain shows no microtubule localization, but does modulate the association of various binding subdomains with microtubules. The acidic carboxy terminus of MAP 4 strongly affects the microtubule binding characteristics of the other domains, despite constituting less than 6% of the protein. These data show that MAP 4 association with microtubules is modulated by sequences both within and outside the basic domain. Further, our work demonstrates that GFP chimeras will allow an in vivo analysis of the effects of MAPs and their variants on microtubule dynamics in real time.

Indexed as

Luminescent ProteinsAnimalsBiomarkersCell CompartmentationCells, CulturedCricetinaeDNA Mutational AnalysisGenes, ReporterGreen Fluorescent ProteinsMicroscopy, FluorescenceMicrotubule-Associated ProteinsMicrotubulesPeptide FragmentsProtein BindingRecombinant Fusion ProteinsStructure-Activity RelationshipBiomarkersGreen Fluorescent ProteinsLuminescent ProteinsMicrotubule-Associated ProteinsPeptide FragmentsRecombinant Fusion Proteins

Identifiers

PMID7622564
PMCPMC2120526
OpenAlexW2082490153

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.