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Updated: Sep 20, 2026

Cytological Analysis of Spermatogenesis: Live and Fixed Preparations of Drosophila Testes
Published on: January 20, 2014
The Drosophila misfire gene has an essential role in sperm activation during fertilization
Takashi Ohsako1, Kazuyuki Hirai, Masa-Toshi Yamamoto
1Drosophila Genetic Resource Center, Kyoto Institute of Technology, Saga Ippongi-cho, Ukyo-ku, Kyoto 816-8354, Japan.
Abstract:
The male sterile mutation, misfire (mfr), of Drosophila melanogaster is a novel paternal effect, fertilization defective mutant that effects sperm head decondensation. mfr sperm were motile, appeared normal morphologically and were transferred to the female during copulation. However, less than 0.1% of eggs laid by females mated to mfr males hatched. Although mfr sperm entered eggs at a high frequency (93%), 99% of the inseminated eggs did not initiate the first nuclear division. Unlike wild type fertilizing sperm, the position and shape of mfr sperm tails within the egg were not constant, but varied in a seemingly random manner. The heads of inseminating mutant sperm were always located near the surface of eggs just underlying the egg plasma membrane, and maintained their needle-like shape indicating the failure of nuclear decondensation. Further observations revealed that plasma membrane of inseminating sperm appeared intact, including the head region. These phenotypes were equivalent to those of sneaky (snky), another fertilization defective male sterile mutation. Our observations strongly suggest that mfr mutant males are sterile because their inseminating sperm fail to form a male pronucleus due to the inability of the sperm to properly respond to egg factors responsible for the breakdown of the plasma membrane. Although mfr and snky mutations were phenotypically identical, they mapped to cytologically distinct genetic loci and no genetic interactions were observed, suggesting that at least two distinct paternal gene products are involved in the early stages of pronuclear formation.
Insights
The male sterile mutation misfire (mfr) in Drosophila prevents sperm head decondensation, causing fertilization failure. This study reveals mfr sperm cannot form a male pronucleus, leading to male sterility.
Area of Science:
- Developmental Biology
- Genetics
- Reproductive Biology
Background:
- Fertilization requires proper sperm function after insemination.
- Paternal effect mutations can disrupt early embryonic development.
- Sperm decondensation is a critical step for male pronucleus formation.
Purpose of the Study:
- To characterize the male sterile mutation misfire (mfr) in Drosophila melanogaster.
- To investigate the role of mfr in sperm function and fertilization.
- To understand the genetic basis of paternal effect sterility.
Main Methods:
- Genetic analysis of the mfr mutation in Drosophila.
- Microscopic observation of sperm behavior within fertilized eggs.
- Phenotypic comparison with other fertilization defective mutants.
Main Results:
- mfr mutant sperm are motile and morphologically normal but fail to decondense their heads after egg entry.
- Inseminated eggs show high sperm penetration but fail to initiate nuclear division (99%).
- mfr sperm heads remain needle-like near the egg surface, indicating failed pronuclear formation.
Conclusions:
- The mfr mutation causes male sterility due to defective sperm head decondensation and failure to form a male pronucleus.
- mfr sperm cannot respond to egg factors necessary for plasma membrane breakdown and pronuclear development.
- Despite identical phenotypes to snky, mfr and snky map to different loci, suggesting distinct genes involved in early pronuclear formation.
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