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Maternal inheritance of functional centrioles in two parthenogenetic nematodes.

Authors :
Perrier, Aurélien
Guiglielmoni, Nadège
Naquin, Delphine
Gorrichon, Kevin
Thermes, Claude
Lameiras, Sonia
Dammermann, Alexander
Schiffer, Philipp H.
Brunstein, Maia
Canman, Julie C.
Dumont, Julien
Source :
Nature Communications; 7/18/2024, Vol. 15 Issue 1, p1-18, 18p
Publication Year :
2024

Abstract

Centrioles are the core constituent of centrosomes, microtubule-organizing centers involved in directing mitotic spindle assembly and chromosome segregation in animal cells. In sexually reproducing species, centrioles degenerate during oogenesis and female meiosis is usually acentrosomal. Centrioles are retained during male meiosis and, in most species, are reintroduced with the sperm during fertilization, restoring centriole numbers in embryos. In contrast, the presence, origin, and function of centrioles in parthenogenetic species is unknown. We found that centrioles are maternally inherited in two species of asexual parthenogenetic nematodes and identified two different strategies for maternal inheritance evolved in the two species. In Rhabditophanes diutinus, centrioles organize the poles of the meiotic spindle and are inherited by both the polar body and embryo. In Disploscapter pachys, the two pairs of centrioles remain close together and are inherited by the embryo only. Our results suggest that maternally-inherited centrioles organize the embryonic spindle poles and act as a symmetry-breaking cue to induce embryo polarization. Thus, in these parthenogenetic nematodes, centrioles are maternally-inherited and functionally replace their sperm-inherited counterparts in sexually reproducing species. Centrioles are broken down during oogenesis and are provided by the sperm during sexual reproduction, though how centriole numbers are regulated during asexual reproduction is unclear. Here they study two asexually reproducing nematodes and identify distinct mechanisms for maternal centrosome inheritance. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
15
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
178529731
Full Text :
https://doi.org/10.1038/s41467-024-50427-5