Evidence map›Paper›PMID 18522719›Full record

ArticleBMC biology2008

Effects of aging and calorie restriction on the global gene expression profiles of mouse testis and ovary.

Alexei A Sharov, Geppino Falco, Yulan Piao, Suresh Poosala, Kevin G Becker, Alan B Zonderman, Dan L Longo, David Schlessinger, Minoru Sh Ko

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

44 citing papers in PubMed, 67 citations in OpenAlex.

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  14. Prediction of ovarian aging using ovarian expression of BMP15, GDF9, and C-KIT.Experimental biology and medicine (Maywood, N.J.) · 2020
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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

9 authors at 3 institutions in 1 country.

Alexei A SharovLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA. SharovAl@grc.nia.nih.gov
Geppino Falco
Yulan Piao
Suresh Poosala
Kevin G Becker
Alan B Zonderman
Dan L Longo
David Schlessinger
Minoru Sh Ko
National Institutes of Health · USInstitute on Aging · USNational Institute on Aging · US

Funding

Analysis of complex biological systems by microarray based gene expressionZICAG000616 · NIA · NATIONAL INSTITUTE ON AGING · PI DE, SUPRIYO · 2009 to 2025
$15.5M
Genes Associated With Ovarian Development and Premature Ovarian Failure - testZIAAG000647 · NIA · NATIONAL INSTITUTE ON AGING · PI SCHLESSINGER, DAVID · 2009 to 2017
$6.2M
Translocations/genes in Premature Ovarian FailureZ01AG000647 · NIA · NATIONAL INSTITUTE ON AGING · PI SCHLESSINGER, DAVID · 1998 to 2008
$1.2M
Analysis of complex biological systems by microarray based gene expressionZ01AG000616 · NIA · NATIONAL INSTITUTE ON AGING · PI BECKER, KEVIN · 2008 to 2008
$886k
CLONING OF A GENE INVOLVED IN SHUTTING OFF CELL GROWTHZ01AG000705 · NIA · NATIONAL INSTITUTE ON AGING · PI KO, MINORU · 1986 to 2008
$303k
Aging of gonads, germ cells, and stem cellsZIAAG000705 · NIA · NATIONAL INSTITUTE ON AGING · PI KO, MINORU · 2009 to 2009
$203k
Intramural NIH HHS
6 · The paper itself

Abstract

backgroundThe aging of reproductive organs is not only a major social issue, but of special interest in aging research. A long-standing view of 'immortal germ line versus mortal soma' poses an important question of whether the reproductive tissues age in similar ways to the somatic tissues. As a first step to understand this phenomenon, we examine global changes in gene expression patterns by DNA microarrays in ovaries and testes of C57BL/6 mice at 1, 6, 16, and 24 months of age. In addition, we compared a group of mice on ad libitum (AL) feeding with a group on lifespan-extending 40% calorie restriction (CR).

resultsWe found that gene expression changes occurred in aging gonads, but were generally different from those in somatic organs during aging. For example, only two functional categories of genes previously associated with aging in muscle, kidney, and brain were confirmed in ovary: genes associated with complement activation were upregulated, and genes associated with mitochondrial electron transport were downregulated. The bulk of the changes in gonads were mostly related to gonad-specific functions. Ovaries showed extensive gene expression changes with age, especially in the period when ovulation ceases (from 6 to 16 months), whereas testes showed only limited age-related changes. The same trend was seen for the effects of CR: CR-mediated reversal of age-associated gene expression changes, reported in somatic organs previously, was limited to a small number of genes in gonads. Instead, in both ovary and testis, CR caused small and mostly gonad-specific effects: suppression of ovulation in ovary and activation of testis-specific genes in testis.

conclusionOverall, the results are consistent with unique modes of aging and its modification by CR in testis and ovary.

Indexed as

Caloric RestrictionGene ExpressionAgingAnimalsFemaleGene Expression ProfilingMaleMiceMice, Inbred C57BLOligonucleotide Array Sequence AnalysisOvaryReverse Transcriptase Polymerase Chain ReactionTestis

Identifiers

PMID18522719
PMCPMC2426674
OpenAlexW2074854140

What OpenQuestion holds

Textmetadata
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.