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

X Xiaoyuan Yan (State Key Laboratory of Soil and Sustainable Agriculture, Changshu National Agro-Ecosystem Observation and Research Station, Institute of Soil Science, Chinese Academy of Sciences) C Chao Wei (Department of Animal Science, Michigan State University) J Jeffrey M. Mann (Department of Animal Science, Michigan State University) G Guanyi Shang (Shanghai 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) Q Qianyi Wang (Department of Chemistry, Michigan State University) H Huirong Xie (Transgenic and Genome Editing Facility, Michigan State University) E Elena Y. Demireva (Transgenic and Genome Editing Facility, Michigan State University) L Liangliang Sun (Department of Chemistry, Michigan State University) D Deqiang Ding (Shanghai 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) C Chen Chen

Abstract

Pachytene piRNAs are the least understood class of piRNAs in the mammalian male germ line. During meiosis, their biogenesis occurs near the 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, resulting in misregulation of MILI, MIWI, and MOV10L1, failure of IMC formation, and an almost 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.

Article Details

Volume / Issue Vol. 123, Issue 20
Published May 19, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (10)

X

Xiaoyuan Yan

State Key Laboratory of Soil and Sustainable Agriculture, Changshu National Agro-Ecosystem Observation and Research Station, Institute of Soil Science, Chinese Academy of Sciences

C

Chao Wei

Department of Animal Science, Michigan State University

J

Jeffrey M. Mann

Department of Animal Science, Michigan State University

G

Guanyi Shang

Shanghai 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

Q

Qianyi Wang

Department of Chemistry, Michigan State University

H

Huirong Xie

Transgenic and Genome Editing Facility, Michigan State University

E

Elena Y. Demireva

Transgenic and Genome Editing Facility, Michigan State University

L

Liangliang Sun

Department of Chemistry, Michigan State University

D

Deqiang Ding

Shanghai 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

C

Chen Chen