Evidence map›Paper›PMID 16600193›Full record

ReviewBrain research2006

Inner ear proteomics of mouse models for deafness, a discovery strategy.

Qing Yin Zheng, Christine R Rozanas, Isolde Thalmann, Mark R Chance, Kumar N Alagramam

Open access · greenAbstract readReview
In one paragraph

Review in Brain research, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
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  4. Identification of target proteins involved in cochlear otosclerosis.Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology · 2015
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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

5 authors at 2 institutions in 1 country.

Qing Yin ZhengThe Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609-1500, USA. qyz@case.edu
Christine R Rozanas
Isolde Thalmann
Mark R Chance
Kumar N Alagramam
Case Western Reserve University · USWashington University in St. Louis · US

Funding

Transcriptome and Proteome Analysis of Mouse Inner EarsR01DC007392 · NIDCD · JACKSON LABORATORY · PI ZHENG, QING Y · 2005 to 2007
$1.0M
Identify and Develop Mouse Models for Otitis MediaR21DC005846 · NIDCD · JACKSON LABORATORY · PI ZHENG, QING Y · 2003 to 2005
$562k
GENETICS OF A NEW MOUSE MODEL FOR DEAFNESSR03DC004376 · NIDCD · JACKSON LABORATORY · PI ZHENG, QING Y · 2000 to 2002
$248k
NIDCD NIH HHS R01 DC007392NIDCD NIH HHS R01DC007392NIDCD NIH HHS R03 DC004376NIDCD NIH HHS R21 DC005846NIDCD NIH HHS R21DC005846
6 · The paper itself

Abstract

Inner ear dysfunction is often associated with defective hair cells. Therefore, hair cells are the focus of study in many of the mouse mutants showing auditory and vestibular deficits. However, harvesting sufficient numbers of hair cells from the tiny bony mouse inner ear for proteomic analysis is challenging. New approaches that would take advantage of mouse mutants and avoid processing steps, such as decalcification or microdissetion, would be more suitable for proteomic analysis. Here, we propose a novel approach called SSUMM-Subtractive Strategy Using Mouse Mutants. SSUMM takes advantage of the differences between control and affected or mutant samples. We predict that SSUMM would be a useful method in proteomics, especially in those cases in which the investigator must work with small numbers of diverse cell types from a tiny organ. Here, we discuss the potential utility of SSUMM to unravel the protein expression profiles of hair cells using the Pou4f3 mouse mutant as an example. Pou4f3 mutant mice exhibit a total loss of inner and outer hair cells, but supporting cells remain relatively intact in the cochlea, thus providing an excellent model for identifying proteins and transcripts that are specific to the hair cell at all life stages. SSUMM would maximize the sensitivity of the analyses while obviating the need for tedious sessions of microdissection and collection of hair cells. By comparing the mutant to control ears at specific time points, it is possible to identify direct targets of a gene product of interest. Further, SSUMM could be used to identify and analyze inner ear development markers and other known genes/proteins that are coexpressed in the ear. In this short technical report, we also discuss protein-profiling approaches suitable for SSUMM and briefly discuss other approaches used in the field of proteomics.

Indexed as

Disease Models, AnimalProteomicsAnimalsDeafnessEar, InnerHumansMiceMice, Mutant Strains

Identifiers

PMID16600193
PMCPMC2853763
OpenAlexW2024944854

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.