Evidence map›Paper›PMID 29883421›Full record

ReviewGenes2018

Influence of Maternal Aging on Mitochondrial Heterogeneity, Inheritance, and Function in Oocytes and Preimplantation Embryos.

Dori C Woods, Konstantin Khrapko, Jonathan L Tilly

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 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
2.6field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. The impact of mitochondrial dysfunction on ovarian aging.Journal of translational medicine · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. The role of mtDNA in oocyte quality and embryo development.Molecular reproduction and development · 2023
    Review
  9. Review
  10. Article
  11. Quercetin protects porcine oocytes fromFrontiers in cell and developmental biology · 2022
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Combining Bioinformatics and Experiments to IdentifyDiagnostics (Basel, Switzerland) · 2020
    Article
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Dori C WoodsLaboratory for Aging and Infertility Research, Department of Biology, Northeastern University, Boston, MA 02115, USA. d.woods@northeastern.edu.
Konstantin KhrapkoLaboratory for Aging and Infertility Research, Department of Biology, Northeastern University, Boston, MA 02115, USA. k.khrapko@northeastern.edu.
Jonathan L TillyLaboratory for Aging and Infertility Research, Department of Biology, Northeastern University, Boston, MA 02115, USA. j.tilly@northeastern.edu.
Northeastern University · US

Funding

Origins/Functions of Mammalian Female Germline Stem CellR37AG012279 · NIA · NORTHEASTERN UNIVERSITY · PI TILLY, JONATHAN LEE · 2006 to 2015
$3.3M
Origins and Functions of Mammalian Female Germline Stem CellsR01AG012279 · NIA · NORTHEASTERN UNIVERSITY · PI TILLY, JONATHAN LEE · 1995 to 2021
$2.7M
NIA NIH HHS R01 AG012279NIA NIH HHS R37 AG012279
6 · The paper itself

Abstract

Contrasting the equal contribution of nuclear genetic material from maternal and paternal sources to offspring, passage of mitochondria, and thus mitochondrial DNA (mtDNA), is uniparental through the egg. Since mitochondria in eggs are ancestral to all somatic mitochondria of the next generation and to all cells of future generations, oocytes must prepare for the high energetic demands of maturation, fertilization and embryogenesis while simultaneously ensuring that their mitochondrial genomes are inherited in an undamaged state. Although significant effort has been made to understand how the mtDNA bottleneck and purifying selection act coordinately to prevent silent and unchecked spreading of invisible mtDNA mutations through the female germ line across successive generations, it is unknown if and how somatic cells of the immediate next generation are spared from inheritance of detrimental mtDNA molecules. Here, we review unique aspects of mitochondrial activity and segregation in eggs and early embryos, and how these events play into embryonic developmental competency in the face of advancing maternal age.

Indexed as

agingembryosinner cell massmitochondriamitochondrial DNAoocytestrophectoderm

Identifiers

PMID29883421
PMCPMC5977205
OpenAlexW2803306064

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.