Evidence map›Paper›PMID 25775403›Full record

ArticlePloS one2015

SEPT12/SPAG4/LAMINB1 complexes are required for maintaining the integrity of the nuclear envelope in postmeiotic male germ cells.

Chung-Hsin Yeh, Pao-Lin Kuo, Ya-Yun Wang, Ying-Yu Wu, Mei-Feng Chen, Ding-Yen Lin, Tsung-Hsuan Lai, Han-Sun Chiang, Ying-Hung Lin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
1.8field-weighted citation impact, top 15% 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, 53 citations in OpenAlex.

  1. Article
  2. SUN5 forms a regular protein lattice reinforcing the sperm head-tail junction.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Protamine 2 deficiency results in Septin 12 abnormalities.Frontiers in cell and developmental biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. The Role of the LINC Complex in Sperm Development and Function.International journal of molecular sciences · 2020
    Review
  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

9 authors at 3 institutions in 1 country.

Chung-Hsin YehDivision of Urology, Department of Surgery, Shin-Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan; School of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan.
Pao-Lin KuoDepartment of Obstetrics & Gynecology, National Cheng Kung University, College of Medicine, Tainan, Taiwan.
Ya-Yun WangDepartment of Obstetrics & Gynecology, National Cheng Kung University, College of Medicine, Tainan, Taiwan.
Ying-Yu WuGraduate Institute of Basic Medicine, Fu Jen Catholic University, College of Medicine, New Taipei City, Taiwan.
Mei-Feng ChenDepartment of Medical Biotechnology and Laboratory Science, Chang Gung University, Tao-Yuan, Taiwan.
Ding-Yen LinInstitute of Bioinformatics and Biosignal Transduction, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan.
Tsung-Hsuan LaiSchool of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan; Department of Obstetrics and Gynecology, Cathay General Hospital, Taipei City, Taiwan; Institute of Systems Biology and Bioinformatics, National Central University, Zhongli City, Taoyuan County, Taiwan.
Han-Sun ChiangSchool of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan; Graduate Institute of Basic Medicine, Fu Jen Catholic University, College of Medicine, New Taipei City, Taiwan.
Ying-Hung LinGraduate Institute of Basic Medicine, Fu Jen Catholic University, College of Medicine, New Taipei City, Taiwan.
Fu Jen Catholic University · TWNational Cheng Kung University · TWChang Gung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Male infertility affects approximately 50% of all infertile couples. The male-related causes of intracytoplasmic sperm injection failure include the absence of sperm, immotile or immature sperm, and sperm with structural defects such as those caused by premature chromosomal condensation and DNA damage. Our previous studies based on a knockout mice model indicated that SEPT12 proteins are critical for the terminal morphological formation of sperm. SEPT12 mutations in men result in teratozospermia and oligozospermia. In addition, the spermatozoa exhibit morphological defects of the head and tail, premature chromosomal condensation, and nuclear damage. However, the molecular functions of SEPT12 during spermatogenesis remain unclear. To determine the molecular functions of SEPT12, we applied a yeast 2-hybrid system to identify SEPT12 interactors. Seven proteins that interact with SEPT12 were identified: SEPT family proteins (SEPT4 and SEPT6), nuclear or nuclear membrane proteins (protamine 2, sperm-associated antigen 4, and NDC1 transmembrane nucleoproine), and sperm-related structural proteins (pericentriolar material 1 and obscurin-like 1). Sperm-associated antigen 4 (SPAG4; also known as SUN4) belongs to the SUN family of proteins and acts as a linker protein between nucleoskeleton and cytoskeleton proteins and localizes in the nuclear membrane. We determined that SEPT12 interacts with SPAG4 in a male germ cell line through coimmunoprecipitation. During human spermiogenesis, SEPT12 is colocalized with SPAG4 near the nuclear periphery in round spermatids and in the centrosome region in elongating spermatids. Furthermore, we observed that SEPT12/SPAG4/LAMINB1 formed complexes and were coexpressed in the nuclear periphery of round spermatids. In addition, mutated SEPT12, which was screened from an infertile man, affected the integration of these nuclear envelope complexes through coimmunoprecipitation. This was the first study that suggested that SEPT proteins link to the SUN/LAMIN complexes during the formation of nuclear envelopes and are involved in the development of postmeiotic germ cells.

Indexed as

Carrier ProteinsHumansLamin Type BMaleMeiosisNuclear EnvelopeProtein BindingSeptinsSpermatogenesisSpermatozoaCarrier ProteinsLamin Type BSEPTIN12 protein, humanSeptinsSPAG4 protein, human

Identifiers

PMID25775403
PMCPMC4361620
OpenAlexW2322474005

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Registered trials

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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.