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Updated: Aug 29, 2026

Mouse Round Spermatid Injection
Published on: January 26, 2024
Mili, a mammalian member of piwi family gene, is essential for spermatogenesis
Satomi Kuramochi-Miyagawa1, Tohru Kimura, Takashi W Ijiri
1Department of Molecular Cell Biology, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamada-oka, Suita-shi, Osaka 565-0871, Japan.
Abstract:
The piwi family genes, which are defined by conserved PAZ and Piwi domains, play important roles in stem cell self-renewal, RNA silencing, and translational regulation in various organisms. To reveal the function of the mammalian homolog of piwi, we produced and analyzed mice with targeted mutations in the Mili gene, which is one of three mouse homologs of piwi. Spermatogenesis in the MILI-null mice was blocked completely at the early prophase of the first meiosis, from the zygotene to early pachytene, and the mice were sterile. However, primordial germ cell development and female germ cell production were not disturbed. Furthermore, MILI bound to MVH, which is an essential factor during the early spermatocyte stage. The similarities in the phenotypes of the MILI- and MVH-deficient mice and in the physical binding properties of MILI and MVH indicate a functional association of these proteins in post-transcriptional regulation. These data indicate that MILI is essential for the differentiation of spermatocytes.
Insights
Mouse Piwi-like 1 (MILI) is crucial for male fertility. MILI-deficient mice exhibit blocked spermatogenesis and sterility, highlighting its essential role in spermatocyte differentiation.
Area of Science:
- Molecular Biology
- Genetics
- Reproductive Biology
Background:
- Piwi family genes are vital for stem cell self-renewal and gene silencing.
- Understanding mammalian Piwi homologs is key to deciphering their roles in development.
Purpose of the Study:
- To investigate the function of the mouse Piwi homolog, Mili.
- To determine the role of MILI in mammalian germ cell development and fertility.
Main Methods:
- Generation and analysis of mice with targeted mutations in the Mili gene (MILI-null mice).
- Phenotypic analysis of germ cell development and spermatogenesis in mutant mice.
- Co-immunoprecipitation assays to assess protein interactions between MILI and MVH.
Main Results:
- MILI-null mice were sterile due to complete blockage of spermatogenesis at the early meiotic prophase (zygotene to early pachytene).
- Primordial germ cell development and female germ cell production were unaffected.
- MILI physically bound to MVH, a known factor in early spermatocyte development.
Conclusions:
- MILI is essential for spermatocyte differentiation and male fertility in mice.
- The physical interaction between MILI and MVH suggests a functional association in post-transcriptional regulation during spermatogenesis.
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