Evidence mapPaperPMID 30359574Full record

ArticleExperimental eye research2019

Proteome-transcriptome analysis and proteome remodeling in mouse lens epithelium and fibers.

Yilin Zhao, Phillip A Wilmarth, Catherine Cheng, Saima Limi, Velia M Fowler, Deyou Zheng, Larry L David, Ales Cvekl

Open access · hybridAbstract read
In one paragraph

Article in Experimental eye research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

37 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  5. Article
  6. Human congenital cataract mutation inInternational journal of ophthalmology · 2025
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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

8 authors at 3 institutions in 2 countries.

Yilin ZhaoDepartments Ophthalmology and Visual Sciences, Albert Einstein College of Medicine, Bronx, NY, 10461, USA; Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Phillip A WilmarthDepartment of Biochemistry & Molecular Biology, Oregon Health Sciences University, 3181 Southwest Sam Jackson Park Road, Portland, OR, 97239, USA.
Catherine ChengDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Saima LimiDepartments Ophthalmology and Visual Sciences, Albert Einstein College of Medicine, Bronx, NY, 10461, USA; Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Velia M FowlerDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Deyou ZhengGenetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA; Neurology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA; Neuroscience, Albert Einstein College of Medicine, Bronx, NY, 10461, USA; Department of Neurosurgery, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200120, China.
Larry L DavidDepartment of Biochemistry & Molecular Biology, Oregon Health Sciences University, 3181 Southwest Sam Jackson Park Road, Portland, OR, 97239, USA.
Ales CveklDepartments Ophthalmology and Visual Sciences, Albert Einstein College of Medicine, Bronx, NY, 10461, USA; Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA. Electronic address: ales.cvekl@einstein.yu.edu.
Albert Einstein College of Medicine · USOregon Health & Science University · USScripps Research Institute · US

Funding

WORD PROCESSORP30CA013330 · YESHIVA UNIVERSITY · 1985 to 2025
$27.5M
TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · YESHIVA UNIVERSITY · 1985 to 2005
$4.6M
Proteomics CoreP30EY010572 · OREGON HEALTH & SCIENCE UNIVERSITY · 1995 to 2025
$4.4M
PAX-6 AS A KEY REGULATOR OF LENS DEVELOPMENTR01EY012200 · YESHIVA UNIVERSITY · 2000 to 2025
$3.0M
Transcriptional control of the Alpha A-crystallin locusR01EY014237 · YESHIVA UNIVERSITY · 2003 to 2005
$1.1M
Eph-ephrin signaling in the lensR01EY032056 · TRUSTEES OF INDIANA UNIVERSITY · 2025 to 2025
$483k
NCI NIH HHS P30 CA013330NEI NIH HHS P30 EY010572NEI NIH HHS R01 EY012200NEI NIH HHS R01 EY014237NEI NIH HHS R01 EY017724NEI NIH HHS R01 EY027768NEI NIH HHS R01 EY032056NEI NIH HHS R21 EY027389NIGMS NIH HHS T32 GM007491
6 · The paper itself

Abstract

Epithelial cells and differentiated fiber cells represent distinct compartments in the ocular lens. While previous studies have revealed proteins that are preferentially expressed in epithelial vs. fiber cells, a comprehensive proteomics library comparing the molecular compositions of epithelial vs. fiber cells is essential for understanding lens formation, function, disease and regenerative potential, and for efficient differentiation of pluripotent stem cells for modeling of lens development and pathology in vitro. To compare protein compositions between the lens epithelium and fibers, we employed tandem mass spectrometry (2D-LC/MS) analysis of microdissected mouse P0.5 lenses. Functional classifications of the top 525 identified proteins into gene ontology categories by molecular processes and subcellular localizations, were adapted for the lens. Expression levels of both epithelial and fiber proteomes were compared with whole lens proteome and mRNA levels using E14.5, E16.5, E18.5, and P0.5 RNA-Seq data sets. During this developmental time window, multiple complex biosynthetic and catabolic processes generate the molecular and structural foundation for lens transparency. As expected, crystallins showed a high correlation between their mRNA and protein levels. Comprehensive data analysis confirmed and/or predicted roles for transcription factors (TFs), RNA-binding proteins (e.g. Carhsp1), translational apparatus including ribosomal heterogeneity and initiation factors, microtubules, cytoskeletal [e.g. non-muscle myosin IIA heavy chain (Myh9) and βB2-spectrin (Sptbn2)] and membrane proteins in lens formation and maturation. Our data highlighted many proteins with unknown functions in the lens that were preferentially enriched in epithelium or fibers, setting the stage for future studies to further dissect the roles of these proteins in fiber cell differentiation vs. epithelial cell maintenance. In conclusion, the present proteomic datasets represent the first mouse lens epithelium and fiber cell proteomes, establish comparative analyses of protein and RNA-Seq data, and characterize the major proteome remodeling required to form the mature lens fiber cells.

Indexed as

AnimalsAnimals, NewbornCell DifferentiationChromatography, LiquidCrystallinsEpithelial CellsFluorescent Antibody Technique, IndirectGene ExpressionGene Expression ProfilingLens, CrystallineMiceProteomeProteomicsRNA, MessengerTandem Mass SpectrometryTranscription FactorsCrystallinsProteomeRNA, MessengerTranscription FactorsDifferentiationLensMass spectrometryProteomeRNA-SeqTranscription factorsTranscriptome

Identifiers

PMID30359574
PMCPMC6360118
OpenAlexW2897780694

What Socratic holds

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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 Socratic graph.