Abstract
Kinesin is a molecular motor that moves along microtubules. Kinesin family member 9 (KIF9) is evolutionarily conserved and expressed strongly in mouse testis. In the unicellular flagellate Chlamydomonas, KLP1 (ortholog of KIF9) is localized to the central pair microtubules of the axoneme and regulates flagellar motility. In contrast, the function of KIF9 remains unclear in mammals. Here, we mutated KIF9 in mice using the CRISPR/Cas9 system. Kif9 mutated mice exhibit impaired sperm motility and subfertility. Further analysis reveals that the flagella lacking KIF9 showed an asymmetric waveform pattern, which leads to a circular motion of spermatozoa. In spermatozoa that lack the central pair protein HYDIN, KIF9 was not detected by immunofluorescence and immunoblot analysis. These results suggest that KIF9 is associated with the central pair microtubules and regulates flagellar motility in mice.
Highlights
Spermatozoa are highly specialized cells that are composed of two parts, head, and flagellum
We revealed that Kinesin family member 9 (KIF9) is localized to the mouse flagellum
KIF9 was detected in the SDS soluble fraction, suggesting that KIF9 is associated with the axoneme
Summary
MEXT | Japan Society for the Promotion of Science (JSPS), Grant/Award Number: JP17H04987, JP17K17852, JP19J12450, JP19J21619 and JP17H01394; Ministry of Education, Culture, Sports, Science and Technology (MEXT), Grant/Award Number: JP25112007 and JP19H05750; Takeda Science Foundation; Japan Agency for Medical Research and Development (AMED), Grant/Award Number: JP19gm5010001; HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Grant/Award Number: P01HD087157 and R01HD088412; Bill and Melinda Gates Foundation (Bill & Melinda Gates Foundation), Grant/Award Number: OPP1160866
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