Evidence map›Paper›PMID 30003673›Full record

ArticleAging cell2018

Proper splicing contributes to visual function in the aging Drosophila eye.

Rachel Stegeman, Hana Hall, Spencer E Escobedo, Henry C Chang, Vikki M Weake

Abstract read
In one paragraph

Article in Aging cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

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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.

Rachel StegemanDepartment of Biochemistry, Purdue University, West Lafayette, Indiana.ORCID 0000-0002-7563-8506
Hana HallDepartment of Biochemistry, Purdue University, West Lafayette, Indiana.ORCID 0000-0002-7544-4437
Spencer E EscobedoDepartment of Biochemistry, Purdue University, West Lafayette, Indiana.ORCID 0000-0002-9026-9104
Henry C ChangDepartment of Biological Sciences, Purdue University, West Lafayette, Indiana.
Vikki M WeakeDepartment of Biochemistry, Purdue University, West Lafayette, Indiana.ORCID 0000-0002-5933-9952

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI Andrea L Kasinski · 1985 to 2026
$43.4M
Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Epigenetic Regulation of Gene Expression in the Aging EyeR01EY024905 · NEI · PURDUE UNIVERSITY · PI WEAKE, VIKKI MARIE · 2015 to 2020
$2.3M
NCATS NIH HHS UL1 TR001108NCI NIH HHS P30 CA023168NEI NIH HHS R01 EY024905NIH HHS P30 CA023168NIH HHS P40 OD018537
6 · The paper itself

Abstract

Changes in splicing patterns are a characteristic of the aging transcriptome; however, it is unclear whether these age-related changes in splicing facilitate the progressive functional decline that defines aging. In Drosophila, visual behavior declines with age and correlates with altered gene expression in photoreceptors, including downregulation of genes encoding splicing factors. Here, we characterized the significance of these age-regulated splicing-associated genes in both splicing and visual function. To do this, we identified differential splicing events in either the entire eye or photoreceptors of young and old flies. Intriguingly, aging photoreceptors show differential splicing of a large number of visual function genes. In addition, as shown previously for aging photoreceptors, aging eyes showed increased accumulation of circular RNAs, which result from noncanonical splicing events. To test whether proper splicing was necessary for visual behavior, we knocked down age-regulated splicing factors in photoreceptors in young flies and examined phototaxis. Notably, many of the age-regulated splicing factors tested were necessary for proper visual behavior. In addition, knockdown of individual splicing factors resulted in changes in both alternative splicing at age-spliced genes and increased accumulation of circular RNAs. Together, these data suggest that cumulative decreases in splicing factor expression could contribute to the differential splicing, circular RNA accumulation, and defective visual behavior observed in aging photoreceptors.

Indexed as

AgingAnimalsBehavior, AnimalDown-RegulationDrosophila melanogasterDrosophila ProteinsEyeGenes, InsectPhotoreceptor Cells, InvertebrateRNARNA, CircularRNA SplicingVision, OcularDrosophila ProteinsRNARNA, CircularagingDrosophilaeyephotoreceptorsplicingvision

Identifiers

PMID30003673
PMCPMC6156539

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.