Evidence map›Paper›PMID 27250771›Full record

ArticleScientific reports2016

Viable offspring obtained from Prm1-deficient sperm in mice.

Naoki Takeda, Kazuya Yoshinaga, Kenryo Furushima, Kazufumi Takamune, Zhenghua Li, Shin-Ichi Abe, Shin-Ichi Aizawa, Ken-Ichi Yamamura

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
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  5. Evaluation ofJournal of the Turkish German Gynecological Association · 2025
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  12. Veterinary sciences · 2022
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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

8 authors at 4 institutions in 2 countries.

Naoki TakedaDivision of Developmental Genetics, Institute of Resource Development and Analysis, Kumamoto University, 2-2-1 Honjo, Kumamoto 860-0811, Japan.
Kazuya YoshinagaDepartment of Anatomy, Graduate School of Health Sciences, Kumamoto University, 4-24-1 Kuhonji, Kumamoto 862-0975, Japan.
Kenryo FurushimaDepartment of Molecular Cell Biology and Molecular Medicine, Institute of Advanced Medicine, Wakayama Medical University, 811-1 Kimiidera, Wakayama 641-8509, Japan.
Kazufumi TakamuneDepartment of Biological Sciences, Graduate School of Science and Technology, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555, Japan.
Zhenghua LiDepartment of Histology and Embryology, Harbin Medical University, Harbin 150081, China.
Shin-Ichi AbeKumamoto Health Science University, 325 Izumi-machi, Kita-ku, Kumamoto 861-5598, Japan.
Shin-Ichi AizawaCenter for Developmental Biology, RIKEN Kobe, 2-2-3 Minatojima Minamimachi, Chuo-ku, Kobe 650-0047, Japan.
Ken-Ichi YamamuraYamamura Project Laboratory, Institute of Resource Development and Analysis, Kumamoto University, Kumamoto 860-0811, Japan.
Kumamoto University · JPHarbin Medical University · CNKumamoto Health Science University · JPWakayama Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protamines are expressed in the spermatid nucleus and allow denser packaging of DNA compared with histones. Disruption of the coding sequence of one allele of either protamine 1 (Prm1) or Prm2 results in failure to produce offspring, although sperm with disrupted Prm1 or Prm2 alleles are produced. Here, we produced Prm1-deficient female chimeric mice carrying Prm1-deficient oocytes. These mice successfully produced Prm1(+/-) male mice. Healthy Prm1(+/-) offspring were then produced by transferring blastocysts obtained via in vitro fertilization using zona-free oocytes and sperm from Prm1(+/-) mice. This result suggests that sperm lacking Prm1 can generate offspring despite being abnormally shaped and having destabilised DNA, decondensed chromatin and a reduction in mitochondrial membrane potential. Nevertheless, these mice showed little derangement of expression profiles.

Indexed as

AnimalsBlastomeresChromatinDNAEmbryo TransferFemaleFertilization in VitroHistonesMaleMembrane Potential, MitochondrialMiceOocytesProtaminesSpermatidsSpermatozoaChromatinDNAHistonesPrm1 protein, mouseProtamines

Identifiers

PMID27250771
PMCPMC4890041
OpenAlexW2419516302

What OpenQuestion holds

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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.