Evidence map›Paper›PMID 24449892›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

TAp73 is required for spermatogenesis and the maintenance of male fertility.

Satoshi Inoue, Richard Tomasini, Alessandro Rufini, Andrew J Elia, Massimiliano Agostini, Ivano Amelio, Dave Cescon, David Dinsdale, Lily Zhou, Isaac S Harris and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
10.6field-weighted citation impact, top 1% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. p53 Controls Meiotic Prophase Progression and Crossover Formation.International journal of molecular sciences · 2022
    Article
  13. Structural diversity of p63 and p73 isoforms.Cell death and differentiation · 2022
    Review
  14. Article
  15. Review
  16. Prevalence of Certain Urogenital BacterialThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2022
    Article
  17. Establishment of an oligoasthenospermia mouse model based onAnimal models and experimental medicine · 2021
    Article
  18. Article
  19. Article
  20. Review

4 more citing papers are in PubMed but not listed here.

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

21 authors at 9 institutions in 4 countries.

Satoshi InoueThe Campbell Family Institute for Breast Cancer Research, Ontario Cancer Institute, University Health Network, Toronto, ON, Canada M5G 2C1.
Richard Tomasini
Alessandro Rufini
Andrew J Elia
Massimiliano Agostini
Ivano Amelio
Dave Cescon
David Dinsdale
Lily Zhou
Isaac S Harris
Sophie Lac
Jennifer Silvester
Wanda Y Li
Masato Sasaki
Jillian Haight
Anne Brüstle
Andrew Wakeham
Colin McKerlie
Andrea Jurisicova
Gerry Melino
Tak W Mak
Ontario Institute for Cancer Research · CAUniversity Health Network · CAMedical Research Council · GBAix-Marseille Université · FRHospital for Sick Children · CAInserm · FRIstituto Dermopatico dell'Immacolata · ITMount Sinai Hospital · CAUniversity of Leicester · GB

Funding

CIHR RN 0000078522Medical Research Council MC_U132670600
6 · The paper itself

Abstract

The generation of viable sperm proceeds through a series of coordinated steps, including germ cell self-renewal, meiotic recombination, and terminal differentiation into functional spermatozoa. The p53 family of transcription factors, including p53, p63, and p73, are critical for many physiological processes, including female fertility, but little is known about their functions in spermatogenesis. Here, we report that deficiency of the TAp73 isoform, but not p53 or ΔNp73, results in male infertility because of severe impairment of spermatogenesis. Mice lacking TAp73 exhibited increased DNA damage and cell death in spermatogonia, disorganized apical ectoplasmic specialization, malformed spermatids, and marked hyperspermia. We demonstrated that TAp73 regulates the mRNA levels of crucial genes involved in germ stem/progenitor cells (CDKN2B), spermatid maturation/spermiogenesis (metalloproteinase and serine proteinase inhibitors), and steroidogenesis (CYP21A2 and progesterone receptor). These alterations of testicular histology and gene expression patterns were specific to TAp73 null mice and not features of mice lacking p53. Our work provides previously unidentified in vivo evidence that TAp73 has a unique role in spermatogenesis that ensures the maintenance of mitotic cells and normal spermiogenesis. These results may have implications for the diagnosis and management of human male infertility.

Indexed as

FertilitySpermatogenesisADAM17 ProteinADAM ProteinsAgingAnimalsApoptosisCell CountCell ProliferationDNA-Binding ProteinsDNA DamageFemaleGene Expression RegulationHumansInfertility, MaleMaleADAM17 ProteinADAM17 protein, humanAdam17 protein, mouseADAM Proteinsdelta Np73 protein, humanDNA-Binding ProteinsMatrix Metalloproteinase 13Mmp13 protein, mouseNuclear ProteinsProgesteroneRNA, MessengerTP73 protein, humanTrp73 protein, mouseTumor Protein p73Tumor Suppressor ProteinsADAM17MMP13SerpinTimp

Identifiers

PMID24449892
PMCPMC3918781
OpenAlexW2074820551

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.