Evidence map›Paper›PMID 17634287›Full record

ArticleMolecular biology of the cell2007

p180 is involved in the interaction between the endoplasmic reticulum and microtubules through a novel microtubule-binding and bundling domain.

Kiyoko Ogawa-Goto, Keiko Tanaka, Tomonori Ueno, Keisuke Tanaka, Takeshi Kurata, Tetsutaro Sata, Shinkichi Irie

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

48 citing papers in PubMed, 83 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

7 authors at 2 institutions in 1 country.

Kiyoko Ogawa-GotoDepartment of Pathology, National Institute of Infectious Diseases, Shinjuku, Tokyo 162-8640, Japan. kgoto@nippi-inc.co.jp
Keiko Tanaka
Tomonori Ueno
Keisuke Tanaka
Takeshi Kurata
Tetsutaro Sata
Shinkichi Irie
National Institute of Infectious Diseases · JPJapan Institute of Leather Research · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

p180 was originally reported as a ribosome-binding protein on the rough endoplasmic reticulum membrane, although its precise role in animal cells has not yet been elucidated. Here, we characterized a new function of human p180 as a microtubule-binding and -modulating protein. Overexpression of p180 in mammalian cells induced an elongated morphology and enhanced acetylated microtubules. Consistently, electron microscopic analysis clearly revealed microtubule bundles in p180-overexpressing cells. Targeted depletion of endogenous p180 by small interfering RNAs led to aberrant patterns of microtubules and endoplasmic reticulum in mammalian cells, suggesting a specific interaction between p180 and microtubules. In vitro sedimentation assays using recombinant polypeptides revealed that p180 bound to microtubules directly and possessed a novel microtubule-binding domain (designated MTB-1). MTB-1 consists of a predicted coiled-coil region and repeat domain, and strongly promoted bundle formation both in vitro and in vivo when expressed alone. Overexpression of p180 induced acetylated microtubules in cultured cells in an MTB-1-dependent manner. Thus, our data suggest that p180 mediates interactions between the endoplasmic reticulum and microtubules mainly through the novel microtubule-binding and -bundling domain MTB-1.

Indexed as

AcetylationAnimalsCells, CulturedChlorocebus aethiopsCHO CellsCOS CellsCricetinaeCricetulusDimerizationEndoplasmic ReticulumGene ExpressionHumansMicrotubulesMutant ProteinsPaclitaxelPeptidesMutant ProteinsPaclitaxelPeptidesReceptors, Cytoplasmic and NuclearRNA, Small Interfering

Identifiers

PMID17634287
PMCPMC1995732
OpenAlexW2107861760

What OpenQuestion holds

Textmetadata
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.