Evidence map›Paper›PMID 35048512›Full record

ArticleAging cell2022

Proper control of R-loop homeostasis is required for maintenance of gene expression and neuronal function during aging.

Juan Jauregui-Lozano, Spencer Escobedo, Alyssa Easton, Nadia A Lanman, Vikki M Weake, Hana Hall

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 40 citations in OpenAlex.

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  9. Lamin A/C loss promotes R-loop-mediated genomic instability and poor survival in small-cell lung cancer.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Review
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  12. Topoisomerase IIIβ protects from tumorigenesis and immune dysregulation.bioRxiv : the preprint server for biology · 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

6 authors at 1 institution in 1 country.

Juan Jauregui-LozanoDepartment of Biochemistry, Purdue University, West Lafayette, Indiana, USA.ORCID 0000-0001-6633-9152
Spencer EscobedoDepartment of Biochemistry, Purdue University, West Lafayette, Indiana, USA.ORCID 0000-0002-9026-9104
Alyssa EastonDepartment of Agricultural and Biological Engineering, Purdue University, West Lafayette, Indiana, USA.ORCID 0000-0002-0972-3630
Nadia A LanmanDepartment of Comparative Pathobiology, College of Veterinary Medicine, Purdue University, West Lafayette, Indiana, USA.ORCID 0000-0002-1819-7070
Vikki M WeakeDepartment of Biochemistry, Purdue University, West Lafayette, Indiana, USA.ORCID 0000-0002-5933-9952
Hana HallDepartment of Biochemistry, Purdue University, West Lafayette, Indiana, USA.ORCID 0000-0002-7544-4437
Purdue University West Lafayette · US

Funding

Epigenetic Regulation of Gene Expression in the Aging EyeR01EY024905 · NEI · PURDUE UNIVERSITY · PI WEAKE, VIKKI MARIE · 2015 to 2020
$2.3M
R-LOOPS AS A NOVEL DRIVER OF PHOTORECEPTOR AGINGR21EY031024 · NEI · PURDUE UNIVERSITY · PI WEAKE, VIKKI MARIE · 2020 to 2021
$371k
NEI NIH HHS R01 EY024905NEI NIH HHS R21 EY031024
6 · The paper itself

Abstract

Age-related loss of cellular function and increased cell death are characteristic hallmarks of aging. While defects in gene expression and RNA metabolism have been linked with age-associated human neuropathies, it is not clear how the changes that occur in aging neurons contribute to loss of gene expression homeostasis. R-loops are RNA-DNA hybrids that typically form co-transcriptionally via annealing of the nascent RNA to the template DNA strand, displacing the non-template DNA strand. Dysregulation of R-loop homeostasis has been associated with both transcriptional impairment and genome instability. Importantly, a growing body of evidence links R-loop accumulation with cellular dysfunction, increased cell death, and chronic disease onset. Here, we characterized the R-loop landscape in aging Drosophila melanogaster photoreceptor neurons and showed that bulk R-loop levels increased with age. Further, genome-wide mapping of R-loops revealed that transcribed genes accumulated R-loops over gene bodies during aging, which correlated with decreased expression of long and highly expressed genes. Importantly, while photoreceptor-specific down-regulation of Top3β, a DNA/RNA topoisomerase associated with R-loop resolution, lead to decreased visual function, over-expression of Top3β or nuclear-localized RNase H1, which resolves R-loops, enhanced positive light response during aging. Together, our studies highlight the functional link between dysregulation of R-loop homeostasis, gene expression, and visual function during aging.

Indexed as

Drosophila melanogasterR-Loop StructuresAgingAnimalsGene ExpressionGenomic InstabilityHomeostasisNeuronsRNATranscription, GeneticRNAagingDrosophilaeyeneuronsphotoreceptorsR-looptranscriptionvisual

Identifiers

PMID35048512
PMCPMC8844117
OpenAlexW4205219648

What OpenQuestion holds

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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.