Evidence map›Paper›PMID 25031318›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2015

Adenine nucleotide translocase 4 is expressed within embryonic ovaries and dispensable during oogenesis.

Chae Ho Lim, Jeffrey V Brower, James L Resnick, S Paul Oh, Naohiro Terada

Open access · bronzeAbstract read
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Interconnected roles of mitochondrial carrier proteins ANT, PFrontiers in molecular biosciences · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. A 20/20 view of ANT function in mitochondrial biology and necrotic cell death.Journal of molecular and cellular cardiology · 2020
    Review
  8. Article
  9. 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

5 authors at 2 institutions in 1 country.

Chae Ho LimDepartment of Pathology, University of Florida College of Medicine, Gainesville, FL, USA.
Jeffrey V BrowerDepartment of Pathology, University of Florida College of Medicine, Gainesville, FL, USA Department of Human Oncology, University of Wisconsin, Madison, WI, USA.
James L ResnickDepartment of Molecular Genetics and Microbiology, University of Florida College of Medicine, Gainesville, FL, USA.
S Paul OhDepartment of Physiology, University of Florida College of Medicine, Gainesville, FL, USA.
Naohiro TeradaDepartment of Pathology, University of Florida College of Medicine, Gainesville, FL, USA terada@pathology.ufl.edu.
Florida College · USUniversity of Florida · US

Funding

Developing Male Contraceptives by Targeting ANT4U01HD060474 · NICHD · UNIVERSITY OF FLORIDA · PI TERADA, NAOHIRO · 2009 to 2013
$1.2M
NICHD NIH HHS U01 HD060474
6 · The paper itself

Abstract

Adenine nucleotide translocase (Ant) facilitates the exchange of adenosine triphosphate across the mitochondrial inner membrane and plays a critical role for bioenergetics in eukaryotes. Mice have 3 Ant paralogs, Ant1 (Slc25a4), Ant2 (Slc25a5), and Ant4 (Slc25a31), which are expressed in a tissue-dependent manner. We previously identified that Ant4 was expressed exclusively in testicular germ cells in adult mice and essential for spermatogenesis and subsequently male fertility. Further investigation into the process of spermatogenesis revealed that Ant4 was particularly highly expressed during meiotic prophase I and indispensable for normal progression of leptotene spermatocytes to the stages thereafter. In contrast, the expression and roles of Ant4 in female germ cells have not previously been elucidated. Here, we demonstrate that the Ant4 gene is expressed during embryonic ovarian development during which meiotic prophase I occurs. We confirmed embryonic ovary-specific Ant4 expression using a bacterial artificial chromosome transgene. In contrast to male, however, Ant4 null female mice were fertile although the litter size was slightly decreased. They showed apparently normal ovarian development which was morphologically indistinguishable from the control animals. These data indicate that Ant4 is a meiosis-specific gene expressed during both male and female gametogenesis however indispensable only during spermatogenesis and not oogenesis. The differential effects of Ant4 depletion within the processes of male and female gametogenesis may be explained by meiosis-specific inactivation of the X-linked Ant2 gene in male, a somatic paralog of the Ant4 gene.

Indexed as

OogenesisAnimalsFemaleFertilityGene Expression Regulation, DevelopmentalGenotypeLitter SizeMaleMeiotic Prophase IMembrane Transport ProteinsMice, Inbred C57BLMice, Inbred DBAMice, KnockoutOvaryPhenotypePromoter Regions, Geneticadenine nucleotide translocase 4, mouseMembrane Transport Proteinsadenine nucleotide translocasemeiosismitochondriaoogenesis

Identifiers

PMID25031318
PMCPMC4287603
OpenAlexW1982577751

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.