Acroframosome-dependent KIFC1 facilitates acrosome formation during spermatogenesis in the caridean shrimp Exopalaemon modestus

PLoS One. 2013 Sep 30;8(9):e76065. doi: 10.1371/journal.pone.0076065. eCollection 2013.

Abstract

Background: Acrosome formation and nuclear shaping are the main events in spermatogenesis. During spermiogenesis in Exopalaemon modestus, a unique microtubular structure called the acroframosome (AFS) forms in spermatids. The AFS links to a temporary organelle called the lamellar complex (LCx) leading to the formation of an everted umbrella-shaped acrosome and a dish-shaped nucleus in the mature sperm. These morphological changes require complex cell motility in which the C-terminal kinesin motor protein called KIFC1 is involved. In this study, we demonstrate that KIFC1 moves along the AFS and plays an important role in acrosome formation and nuclear shaping during spermatogenesis in E. modestus.

Methodology/principal findings: We cloned a 3125 bp complete cDNA of kifc1 from the testis of E. modestus by PCR. The predicted secondary and tertiary structures of E. modestus KIFC1 contain three domains: a) the C-terminus, b) the stalk region, and the c) N-terminusl. Semi-quantitative RT-PCR detected the expression of kifc1 mRNA in different tissues of E. modestus. In situ hybridization demonstrated the temporal and spatial expression profile of kifc1 during spermiogenesis. Western blot identified the expression of KIFC1 in different tissues of E. modestus, including the testis. Immunofluorescence localized KIFC1, tubulin, GM130, and mitochondria in order to elucidate their role during spermiogenesis in E. modestus.

Conclusion/significance: Our results indicate that KIFC1 transports the Golgi complex, mitochondria, and other cellular components that results in acrosome formation and nuclear shaping in E. modestus. The KIFC1 transport function depends upon the microtubular structure called the acroframosome (AFS). This study describes some of the molecular mechanisms involved in the acrosome formation and nuclear shaping in E. modestus. In addition, this study may provide a model for studying the molecular mechanisms involved in spermatogenesis in other crustacean species and lead to a better understanding of the fertilization process in crustaceans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrosome / physiology*
  • Animals
  • Base Sequence
  • Blotting, Western
  • Cell Movement / physiology
  • China
  • Cloning, Molecular
  • Cluster Analysis
  • Computational Biology
  • DNA Primers / genetics
  • DNA, Complementary / genetics
  • Fluorescent Antibody Technique
  • In Situ Hybridization
  • Kinesins / genetics
  • Kinesins / metabolism*
  • Male
  • Microscopy, Electron, Transmission
  • Microtubules / metabolism
  • Microtubules / physiology*
  • Molecular Sequence Data
  • Palaemonidae / genetics
  • Palaemonidae / physiology*
  • Phylogeny
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • Spermatogenesis / physiology*

Substances

  • DNA Primers
  • DNA, Complementary
  • Kinesins

Grants and funding

This work was supported by National Natural Science Foundation of China (No. 41276151 and 31072198). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.