Evidence map›Paper›PMID 18625841›Full record

ArticleThe Journal of cell biology2008

Mars promotes dTACC dephosphorylation on mitotic spindles to ensure spindle stability.

Shengjiang Tan, Ekaterina Lyulcheva, Jon Dean, Daimark Bennett

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Shengjiang TanDepartment of Zoology, Oxford University, Oxford OX1 3PS, England, UK.
Ekaterina Lyulcheva
Jon Dean
Daimark Bennett
University of Liverpool · GBUniversity of Oxford · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/B/11869Cancer Research UK
6 · The paper itself

Abstract

Microtubule-associated proteins (MAPs) ensure the fidelity of chromosome segregation by controlling microtubule (MT) dynamics and mitotic spindle stability. However, many aspects of MAP function and regulation are poorly understood in a developmental context. We show that mars, which encodes a Drosophila melanogaster member of the hepatoma up-regulated protein family of MAPs, is essential for MT stabilization during early embryogenesis. As well as associating with spindle MTs in vivo, Mars binds directly to protein phosphatase 1 (PP1) and coimmunoprecipitates from embryo extracts with minispindles and Drosophila transforming acidic coiled-coil (dTACC), two MAPs that function as spindle assembly factors. Disruption of binding to PP1 or loss of mars function results in elevated levels of phosphorylated dTACC on spindles. A nonphosphorylatable form of dTACC is capable of rescuing the lethality of mars mutants. We propose that Mars mediates spatially controlled dephosphorylation of dTACC, which is critical for spindle stabilization.

Indexed as

AnimalsDrosophila melanogasterDrosophila ProteinsMicrotubule-Associated ProteinsMutationNerve Tissue ProteinsPhosphorylationProtein BindingProtein Phosphatase 1Protein TransportSAP90-PSD95 Associated ProteinsSpindle ApparatusDrosophila ProteinsMars protein, DrosophilaMicrotubule-Associated ProteinsNerve Tissue ProteinsProtein Phosphatase 1SAP90-PSD95 Associated ProteinsTACC protein, Drosophila

Identifiers

PMID18625841
PMCPMC2447907
OpenAlexW2046802544

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.