The Evolution of Centriole Degradation in Mouse Sperm
Authors:
- Sushil KhanalSKSushil Khanal
- Ankit JaiswalAJAnkit Jaiswal
- Rajanikanth ChowdanayakaRCRajanikanth Chowdanayaka
- Nahshon PuenteNPNahshon Puente
- Katerina TurnerKTKaterina Turner
- Kebron Yeshitela AssefaKAKebron Yeshitela Assefa
- Mohamad NawrasMNMohamad Nawras
- Ezekiel David BackEBEzekiel David Back
- Abigail RoyfmanARAbigail Royfman
- James P. BurkettJBJames P. Burkett
- Soon Hon CheongSCSoon Hon Cheong
- Heidi S. FisherHeidi S. Fisher
Preprint
Abstract
Centrioles are subcellular organelles found at the cilia base with an evolutionarily conserved structure and a shock absorber-like function. In sperm, centrioles are found at the flagellum base and are essential for embryo development in basal animals. Yet, sperm centrioles have evolved diverse forms, sometimes acting like a transmission system, as in cattle, and sometimes becoming dispensable, as in house mice. How the essential sperm centriole evolved to become dispensable in some organisms is unclear. Here, we test the hypothesis that this transition occurred through a cascade of evolutionary changes to the proteins, structure, and function of sperm centrioles and was possibly driven by sperm competition. We found that the final steps in this cascade are associated with a change in the primary structure of the centriolar luminal protein FAM161A in rodents. This information provides the first insight into the molecular mechanisms and adaptive evolution underlying a major evolutionary transition within the internal structure of the mammalian sperm neck. Graphical Highlights: – Barrel-shaped centrioles are present in all rodents except members of the Muridae taxonomical family. – The FAM161A sequence evolved selectively in rodents and specifically in a murid subgroup. – The evolution of centriole degradation is correlated with the expression of a novel FAM161A isoform. – The ancestral centriole remodeling program involves elongation followed by redistribution. – The mouse centriole degradation program involves elongation followed by elimination.Keywords
All Related Versions
- Published version: Nature Communications, 15 (1), 1.
This publication has 148 references indexed in Scilit:
- The transition from meiotic to mitotic spindle assembly is gradual during early mammalian developmentJournal of Cell Biology, 2012
- MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model SpaceSystematic Biology, 2012
- Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis PigmentosaThe American Journal of Human Genetics, 2010
- Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis PigmentosaThe American Journal of Human Genetics, 2010
- hPOC5 is a centrin-binding protein required for assembly of full-length centriolesJournal of Cell Biology, 2009
- TSKS concentrates in spermatid centrioles during flagellogenesisDevelopmental Biology, 2008
- The zebrafish maternal-effect gene cellular atoll encodes the centriolar component sas-6 and defects in its paternal function promote whole genome duplicationDevelopmental Biology, 2007
- PAML 4: Phylogenetic Analysis by Maximum LikelihoodMolecular Biology and Evolution, 2007
- MUSCLE: multiple sequence alignment with high accuracy and high throughputNucleic Acids Research, 2004
- The rapid evolution of reproductive proteinsNature Reviews Genetics, 2002