A Highly Conserved Poc1 Protein Characterized in Embryos of the Hydrozoan Clytia hemisphaerica: Localization and Functional Studies

Poc1 (Protein of Centriole 1) proteins are highly conserved WD40 domain-containing centriole components, well characterized in the alga Chlamydomonas, the ciliated protazoan Tetrahymena, the insect Drosophila and in vertebrate cells including Xenopus and zebrafish embryos. Functions and localizations related to the centriole and ciliary axoneme have been demonstrated for Poc1 in a range of species. The vertebrate Poc1 protein has also been reported to show an additional association with mitochondria, including enrichment in the specialized “germ plasm” region of Xenopus oocytes. We have identified and characterized a highly conserved Poc1 protein in the cnidarian Clytia hemisphaerica. Clytia Poc1 mRNA was found to be strongly expressed in eggs and early embryos, showing a punctate perinuclear localization in young oocytes. Fluorescence-tagged Poc1 proteins expressed in developing embryos showed strong localization to centrioles, including basal bodies. Anti-human Poc1 antibodies decorated mitochondria in Clytia, as reported in human cells, but failed to recognise endogenous or fluorescent-tagged Clytia Poc1. Injection of specific morpholino oligonucleotides into Clytia eggs prior to fertilization to repress Poc1 mRNA translation interfered with cell division from the blastula stage, likely corresponding to when neosynthesis normally takes over from maternally supplied protein. Cell cycle lengthening and arrest were observed, phenotypes consistent with an impaired centriolar biogenesis or function. The specificity of the defects could be demonstrated by injection of synthetic Poc1 mRNA, which restored normal development. We conclude that in Clytia embryos, Poc1 has an essentially centriolar localization and function

Sperm competition and sperm length influence the rate of mammalian spermatogenesis

Sperm competition typically favours an increased investment in testes, because larger testes can produce more sperm to provide a numerical advantage in competition with rival ejaculates. However, interspecific variation in testis size cannot be equated directly with variation in sperm production rate—which is the trait ultimately selected under sperm competition—because there are also differences between species in the proportion of spermatogenic tissue contained within the testis and in the time it takes to produce each sperm. Focusing on the latter source of variation, we provide phylogenetically controlled evidence for mammals that species with relatively large testes (and hence a high level of sperm competition) have a shorter duration of the cycle of the seminiferous epithelium and consequently a faster rate of spermatogenesis, enabling males to produce more sperm per unit testis per unit time. Moreover, we identify an independent negative relationship between sperm length and the rate of spermatogenesis, such that spermatogenesis takes longer in species with longer sperm. We conclude that sperm competition selects for both larger testes and a faster rate of spermatogenesis to increase overall sperm production, and that an evolutionary trade-off between sperm size and numbers may be mediated via constraints on the rate of spermatogenesis imposed by selection for longer sperm