Evidence map›Paper›PMID 26589352›Full record

ArticleEMBO reports2016

Dead end1 is an essential partner of NANOS2 for selective binding of target RNAs in male germ cell development.

Atsushi Suzuki, Yuki Niimi, Kaori Shinmyozu, Zhi Zhou, Makoto Kiso, Yumiko Saga

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

62 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Gonocytes in Transition: Establishing the Male Germline Identity.Advances in experimental medicine and biology · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. P-body-like condensates in the germline.Seminars in cell & developmental biology · 2024
    Review
  15. Article
  16. Article
  17. Cell cycle regulation for meiosis in mammalian germ cells.The Journal of reproduction and development · 2023
    Review
  18. Article
  19. Article
  20. Article

2 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

6 authors at 3 institutions in 1 country.

Atsushi SuzukiDivision of Materials Science and Chemical Engineering, Faculty of Engineering, Yokohama National University, Yokohama Kanagawa, Japan atsuzuki@ynu.ac.jp ysaga@lab.nig.ac.jp.
Yuki NiimiDivision of Materials Science and Chemical Engineering, Graduate School of Engineering Yokohama National University, Yokohama Kanagawa, Japan.
Kaori ShinmyozuMass Spectrometric Unit, RIKEN Center for Developmental Biology, Kobe Hyogo, Japan.
Zhi ZhouDivision of Mammalian Development, National Institute of Genetics, Mishima Shizuoka, Japan.
Makoto KisoDivision of Mammalian Development, National Institute of Genetics, Mishima Shizuoka, Japan.
Yumiko SagaDivision of Mammalian Development, National Institute of Genetics, Mishima Shizuoka, Japan atsuzuki@ynu.ac.jp ysaga@lab.nig.ac.jp.
National Institute of Genetics · JPYokohama National University · JPRIKEN Center for Computational Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA-binding proteins (RBPs) play important roles for generating various cell types in many developmental processes, including eggs and sperms. Nanos is widely known as an evolutionarily conserved RNA-binding protein implicated in germ cell development. Mouse NANOS2 interacts directly with the CCR4-NOT (CNOT) deadenylase complex, resulting in the suppression of specific RNAs. However, the mechanisms involved in target specificity remain elusive. We show that another RBP, Dead end1 (DND1), directly interacts with NANOS2 to load unique RNAs into the CNOT complex. This interaction is mediated by the zinc finger domain of NANOS2, which is essential for its association with target RNAs. In addition, the conditional deletion of DND1 causes the disruption of male germ cell differentiation similar to that observed in Nanos2-KO mice. Thus, DND1 is an essential partner for NANOS2 that leads to the degradation of specific RNAs. We also present the first evidence that the zinc finger domain of Nanos acts as a protein-interacting domain for another RBP, providing a novel insight into Nanos-mediated germ cell development.

Indexed as

Cell DifferentiationAnimalsCarrier ProteinsEmbryonic Germ CellsGene Expression Regulation, DevelopmentalMaleMice, KnockoutNeoplasm ProteinsProtein Interaction Domains and MotifsRNARNA-Binding ProteinsSpermatozoaZinc FingersCarrier ProteinsDnd1 protein, mouseNanos2 protein, mouseNeoplasm ProteinsRNARNA-Binding ProteinsDead endgerm cellNanosRNA

Identifiers

PMID26589352
PMCPMC4718414
OpenAlexW2174949379

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.