Evidence map›Paper›PMID 36912526›Full record

ArticleJournal of visualized experiments : JoVE2023

Cell-Specific Paired Interrogation of the Mouse Ovarian Epigenome and Transcriptome.

Sarah R Ocañas, José V V Isola, Tatiana D Saccon, Kevin D Pham, Ana J Chucair-Elliott, Augusto Schneider, Willard M Freeman, Michael B Stout

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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.

Sarah R Ocañas *Aging and Metabolism Research Program, Oklahoma Medical Research Foundation; Genes & Human Disease Research Program, Oklahoma Medical Research Foundation; Oklahoma City Veterans Affairs Medical Center.
José V V Isola *Aging and Metabolism Research Program, Oklahoma Medical Research Foundation; Oklahoma City Veterans Affairs Medical Center.
Tatiana D SacconAging and Metabolism Research Program, Oklahoma Medical Research Foundation.
Kevin D PhamGenes & Human Disease Research Program, Oklahoma Medical Research Foundation.
Ana J Chucair-ElliottGenes & Human Disease Research Program, Oklahoma Medical Research Foundation.
Augusto SchneiderNutrition College, Federal University of Pelotas.
Willard M FreemanGenes & Human Disease Research Program, Oklahoma Medical Research Foundation; Oklahoma City Veterans Affairs Medical Center.
Michael B StoutAging and Metabolism Research Program, Oklahoma Medical Research Foundation; Oklahoma City Veterans Affairs Medical Center; michael-stout@omrf.org.
Oklahoma Medical Research Foundation · USUniversidade Federal de Pelotas · BRVeterans Health Administration · US

Funding

GEROSCIENCE TRAINING PROGRAM IN OKLAHOMAT32AG052363 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Benjamin Francis Miller, William Edmund Sonntag · 2017 to 2026
$3.6M
Role of estrogen receptor-a in aging and sex-specific responses to 17a-estradiolR01AG070035 · NIA · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI STOUT, MICHAEL B · 2021 to 2025
$2.6M
Cellular senescence and epigenomic remodeling in ovarian agingR01AG069742 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI STOUT, MICHAEL B · 2020 to 2024
$2.0M
Dynamics of the brain epigenome with agingI01BX003906 · VA · OKLAHOMA CITY VA MEDICAL CENTER · PI FREEMAN, WILLARD M · 2018 to 2021
–
BLRD VA I01 BX003906BLRD VA IK6 BX006033NIA NIH HHS R01 AG069742NIA NIH HHS R01 AG070035NIA NIH HHS T32 AG052363
6 · The paper itself

Abstract

Assessing cell-type-specific epigenomic and transcriptomic changes are key to understanding ovarian aging. To this end, the optimization of the translating ribosome affinity purification (TRAP) method and the isolation of nuclei tagged in specific cell types (INTACT) method was performed for the subsequent paired interrogation of the cell-specific ovarian transcriptome and epigenome using a novel transgenic NuTRAP mouse model. The expression of the NuTRAP allele is under the control of a floxed STOP cassette and can be targeted to specific ovarian cell types using promoter-specific Cre lines. Since recent studies have implicated ovarian stromal cells in driving premature aging phenotypes, the NuTRAP expression system was targeted to stromal cells using a Cyp17a1-Cre driver. The induction of the NuTRAP construct was specific to ovarian stromal fibroblasts, and sufficient DNA and RNA for sequencing studies were obtained from a single ovary. The NuTRAP model and methods presented here can be used to study any ovarian cell type with an available Cre line.

Indexed as

EpigenomeTranscriptomeAnimalsFemaleGene Expression ProfilingMiceMice, TransgenicOvary

Identifiers

PMID36912526
PMCPMC10165884
OpenAlexW4321763664

What OpenQuestion holds

Textmetadata
LicenceTDM
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.