Evidence map›Paper›PMID 41280110›Full record

ArticlebioRxiv : the preprint server for biology2025

Spatiotemporal control of PIWI compartmentalization by mitochondrial scaffolds defines pachytene piRNA pathway organization.

Xiaoyuan Yan, Chao Wei, Jeffrey M Mann, Guanyi Shang, Qianyi Wang, Huirong Xie, Elena Y Demireva, Liangliang Sun, Deqiang Ding, Chen Chen

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Xiaoyuan YanDepartment of Animal Science, Michigan State University, East Lansing, MI 48824, USA.
Chao WeiDepartment of Animal Science, Michigan State University, East Lansing, MI 48824, USA.
Jeffrey M MannDepartment of Animal Science, Michigan State University, East Lansing, MI 48824, USA.
Guanyi ShangShanghai Key Laboratory of Maternal and 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, China.
Qianyi WangDepartment of Chemistry, Michigan State University, East Lansing, MI 48824, USA.
Huirong XieTransgenic and Genome Editing Facility, Michigan State University, East Lansing, MI 48824, USA.
Elena Y DemirevaTransgenic and Genome Editing Facility, Michigan State University, East Lansing, MI 48824, USA.
Liangliang SunDepartment of Chemistry, Michigan State University, East Lansing, MI 48824, USA.
Deqiang DingShanghai Key Laboratory of Maternal and 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, China.
Chen ChenDepartment of Animal Science, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0001-9159-4489

Funding

Tudor Domain Proteins in Germline Genome DefenseR01HD084494 · NICHD · MICHIGAN STATE UNIVERSITY · PI CHEN, CHEN · 2015 to 2023
$3.0M
Mitochondria-anchored protein complexes in piRNA biogenesis and functionR01GM132490 · NIGMS · MICHIGAN STATE UNIVERSITY · PI CHEN, CHEN · 2019 to 2022
$1.2M
Genetic and biochemical dissection of mammalian pachytene piRNA biogenesis.R35GM156209 · NIGMS · MICHIGAN STATE UNIVERSITY · PI Chen Chen · 2025 to 2026
$846k
NICHD NIH HHS R01 HD084494NIGMS NIH HHS R01 GM132490NIGMS NIH HHS R35 GM156209
6 · The paper itself

Abstract

Pachytene piRNAs are the least understood class of piRNAs in the mammalian male germ line. During meiosis, their biogenesis occurs near mitochondrial outer membrane in germ granules known as intermitochondrial cement (IMC). However, how mitochondrial factors regulate the trafficking of PIWI proteins into and out of the IMC remain poorly understood. Here we show that the cytoplasmic PIWI proteins MILI and MIWI are recruited for pachytene piRNA biogenesis via distinct mitochondrial membrane proteins. Loss of the mitochondrial scaffold protein ASZ1 during meiosis in mice disrupts multiple downstream biogenesis steps, leading to misregulation of MILI and MIWI, failure of IMC formation, and a near-complete loss of mature pachytene piRNAs. Strikingly, despite the drastic depletion of pachytene piRNAs, LINE1 transposon silencing remains unaffected. We identify three classes of pachytene piRNA pathway components that coordinate piRNA production and compartmentalization. Our findings reveal that chromatoid body precursors serve as a central hub for the accumulation of pachytene PIWI-piRNA complexes, thus establishing a connection between IMC-based biogenesis and downstream piRNA function.

Identifiers

PMID41280110
PMCPMC12637698

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.