Evidence map›Paper›PMID 24244856›Full record

ArticleBiology open2013

Marshalin, a microtubule minus-end binding protein, regulates cytoskeletal structure in the organ of Corti.

Jing Zheng, David Furness, Chongwen Duan, Katharine K Miller, Roxanne M Edge, Jessie Chen, Kazuaki Homma, Carole M Hackney, Peter Dallos, Mary Ann Cheatham

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  4. CAMSAP3 facilitates basal body polarity and the formation of the central pair of microtubules in motile cilia.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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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

10 authors at 4 institutions in 3 countries.

Jing ZhengDepartment of Otolaryngology - Head and Neck Surgery, Feinberg School of Medicine, Northwestern University , Chicago, IL 60611 , USA ; Hugh Knowles Center for Clinical and Basic Science in Hearing and Its Disorders, Northwestern University , Evanston, IL 60208 , USA.
David Furness
Chongwen Duan
Katharine K Miller
Roxanne M Edge
Jessie Chen
Kazuaki Homma
Carole M Hackney
Peter Dallos
Mary Ann Cheatham
Northwestern University · USKeele University · GBUniversität Hamburg · DEUniversity of Sheffield · GB

Funding

STUDIES IN COCHLEAR HAIR CELL TRANSDUCTIONR01DC000089 · NIDCD · NORTHWESTERN UNIVERSITY · PI CHEATHAM, MARY ANN · 1989 to 2015
$10.1M
DYNAMIC INTERATION AMONG PROTEINS IN HAIR CELLSR01DC011813 · NIDCD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZHENG, JING · 2012 to 2016
$1.6M
NIDCD NIH HHS R01 DC000089NIDCD NIH HHS R01 DC011813
6 · The paper itself

Abstract

Dramatic structural changes in microtubules (MT) and the assembly of complicated intercellular connections are seen during the development of the cellular matrix of the sense organ for hearing, the organ of Corti. This report examines the expression of marshalin, a minus-end binding protein, during this process of cochlear development. We discovered that marshalin is abundantly expressed in both sensory hair cells and supporting cells. In the adult, prominent marshalin expression is observed in the cuticular plates of hair cells and in the noncentrosomal MT organization centers (MTOC) of Deiters' and pillar cells. Based upon differences in marshalin expression patterns seen in the organ of Corti, we identified eight isoforms ranging from 863 to 1280 amino acids. mRNAs/proteins associated with marshalin's isoforms are detected at different times during development. These isoforms carry various protein-protein interacting domains, including coiled-coil (CC), calponin homology (CH), proline-rich (PR), and MT-binding domains, referred to as CKK. We, therefore, examined membranous organelles and structural changes in the cytoskeleton induced by expressing two of these marshalin isoforms in vitro. Long forms containing CC and PR domains induce thick, spindle-shaped bundles, whereas short isoforms lacking CC and PR induce more slender variants that develop into densely woven networks. Together, these data suggest that marshalin is closely associated with noncentrosomal MTOCs, and may be involved in MT bundle formation in supporting cells. As a scaffolding protein with multiple isoforms, marshalin is capable of modifying cytoskeletal networks, and consequently organelle positioning, through interactions with various protein partners present in different cells.

Indexed as

CAMSAP3CochleaMicrotubule minus-end binding proteinNezhaNoncentrosomal MTOCPatronin

Identifiers

PMID24244856
PMCPMC3828766
OpenAlexW2170853403

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.