Evidence map›Paper›PMID 41023308›Full record

ArticleThe EMBO journal2025

PIWI proteins tether the piRNA biogenesis machinery to mitochondria during mammalian spermatogenesis.

Jie Gao, Canmei Chen, Guanyi Shang, Wenyang Yu, Ting Zhao, Yunfang Zhang, Chen Chen, Deqiang Ding

Abstract read
In one paragraph

Article in The EMBO journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Spatiotemporal control of PIWI compartmentalization by mitochondrial scaffolds defines pachytene piRNA pathway organization.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Review
  6. Review
  7. 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

8 authors.

Jie Gao *Shanghai Key Laboratory of Maternal Fetal Medicine, Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, 200092, China.
Canmei Chen *Shanghai Key Laboratory of Maternal Fetal Medicine, Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, 200092, China.
Guanyi ShangShanghai Key Laboratory of Maternal Fetal Medicine, Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, 200092, China.
Wenyang YuShanghai Key Laboratory of Maternal Fetal Medicine, Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, 200092, China.
Ting ZhaoShanghai Key Laboratory of Maternal Fetal Medicine, Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, 200092, China.
Yunfang ZhangShanghai Key Laboratory of Maternal Fetal Medicine, Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, 200092, China.ORCID http://orcid.org/0000-0001-9529-0431
Chen ChenDepartment of Animal Science, Michigan State University, East Lansing, MI, 48824, USA.
Deqiang DingShanghai Key Laboratory of Maternal Fetal Medicine, Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, 200092, China. dingdeqiang@tongji.edu.cn.ORCID http://orcid.org/0000-0002-7959-5654

Funding

Tudor Domain Proteins in Germline Genome DefenseR01HD084494 · NICHD · MICHIGAN STATE UNIVERSITY · PI CHEN, CHEN · 2015 to 2023
$3.0M
Genetic and biochemical dissection of mammalian pachytene piRNA biogenesis.R35GM156209 · NIGMS · MICHIGAN STATE UNIVERSITY · PI Chen Chen · 2025 to 2026
$846k
HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) R01HD084494HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM156209MOST | National Key Research and Development Program of China (NKPs) 2022YFA1305300MOST | National Natural Science Foundation of China (NSFC) 32470901NICHD NIH HHS R01 HD084494NIGMS NIH HHS R35 GM156209
6 · The paper itself

Abstract

piRNA biogenesis occurs in the intermitochondrial cement (IMC) in mammalian germ cells. The mechanisms by which IMC components engage mitochondria to form an efficient piRNA biogenesis machinery remain elusive. Here, we demonstrate that PIWI proteins orchestrate the assembly and disassembly of the piRNA biogenesis machinery in mice. The mitochondrial-anchored protein ASZ1 specifically interacts with PIWIL2 and recruits PIWIL2 to IMC granules. Sequentially, piRNAs competitively bind PIWIL2, leading to ASZ1-PIWIL2 dissociation. In fetal male germ cells, ASZ1-PIWIL2-TDRD1 forms a seed complex to initiate the assembly of the piRNA biogenesis machinery. During postnatal meiosis, the TDRKH-PIWIL1-TDRD1 complex synergizes with the ASZ1-PIWIL2-TDRD1 complex to induce substantial IMC assembly and pachytene piRNA biogenesis through TDRD1-mediated phase separation. PIWI proteins act as bridges, tethering non-mitochondrial proteins to mitochondrial-anchored proteins in IMC granules with the assistance of TDRD1. Together, our findings establish the pivotal role of PIWI proteins in governing the spatiotemporal dynamics of piRNA biogenesis machinery during mammalian spermatogenesis.

Indexed as

Argonaute ProteinsMitochondriaRNA, Small InterferingSpermatogenesisAnimalsCell Cycle ProteinsMaleMiceMitochondrial ProteinsPiwi-Interacting RNAProteinsRNA-Binding ProteinsArgonaute ProteinsCell Cycle ProteinsMitochondrial ProteinsPiwi-Interacting RNAPiwil1 protein, mousePiwil2 protein, mouseProteinsRNA-Binding ProteinsRNA, Small InterferingTdrd1 protein, mouseTdrkh protein, mouseGerm GranuleMitochondrionPIWI-Interacting RNAPIWI ProteinSpermatogenesis

Identifiers

PMID41023308
PMCPMC12624062

What Socratic 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 Socratic graph.