Evidence map›Paper›PMID 29329412›Full record

ArticleBiology of reproduction2018

Lhx8 ablation leads to massive autophagy of mouse oocytes associated with DNA damage.

Laura D'Ignazio, Marc Michel, Melissa Beyer, Kassimier Thompson, Antonino Forabosco, David Schlessinger, Emanuele Pelosi

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-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

15 citing papers in PubMed, 34 citations in OpenAlex.

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  15. Autophagy in hypoxic ovary.Cellular and molecular life sciences : CMLS · 2019
    Review
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

7 authors at 3 institutions in 1 country.

Laura D'IgnazioIntramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Marc MichelIntramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Melissa BeyerIntramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Kassimier ThompsonIntramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Antonino ForaboscoGenomic Research Centre, Cante di Monteveccio Association, Fano, Italy.
David SchlessingerIntramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
Emanuele PelosiIntramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.
National Institutes of Health · USNational Institute on Aging · USInstitute on Aging · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Following proliferation of oogonia in mammals, great numbers of germ cells are discarded, primarily by apoptosis, while the remainder form primordial follicles (the ovarian reserve) that determine fertility and reproductive lifespan. More massive, rapid, and essentially total loss of oocytes, however, occurs when the transcription factor Lhx8 is ablated-though the cause and mechanism of germ cell loss from the Lhx8-/- ovaries has been unknown. We found that Lhx8-/- ovaries maintain the same number of germ cells throughout embryonic development; rapid decrease in the pool of oocytes starts shortly before birth. The loss results from activation of autophagy, which becomes overwhelming within the first postnatal week, with extracellular matrix proteins filling the space previously occupied by follicles to produce a fibrotic ovary. Associated with this process, as early as a few days before birth, Lhx8-/- oocytes failed to repair DNA damage-which normally occurs when meiosis is initiated during embryonic development; and DNA damage repair genes were downregulated throughout the oocyte short lifespan. Based on gene expression analyses and morphological changes, we propose a model in which lineage-restricted failure of DNA repair triggers germ cell autophagy, causing premature depletion of the ovarian reserve in Lhx8-/- mice.

Indexed as

AnimalsApoptosisAutophagyDNA DamageFemaleLIM-Homeodomain ProteinsMeiosisMiceMice, KnockoutOocytesOogenesisOogoniaOvarian ReserveTranscription FactorsLIM homeobox protein 8LIM-Homeodomain ProteinsTranscription Factors

Identifiers

PMID29329412
PMCPMC6279113
OpenAlexW2784328279

What OpenQuestion holds

Textmetadata
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.