Delattre, M. | Search bioRxiv

bioRxiv2018

Why would parthenogenetic females systematically produce males who never transmit their genes to females?

SummaryIn pseudogamous species, females use the sperm of males from another species to activate their oocytes and produce females, without using the sperm DNA. Here we report a novel reproductive strategy found in the pseudogamous nematode Mesorhabditis belari, which produces its own males at low frequency. We find that the 8% of M. belari males are necessary to fertilize all oocytes but pass on their genes only to males, and never to females. Thus, the production of males has no impact on the genetic diversity of females. Using game theory, we show that the production of males at low frequency constitutes an efficient strategy only if sons are more likely to mate with their sisters. We validate this prediction experimentally by revealing a mating preference between siblings. We uncover the remarkable reproductive strategy of parthenogenetic females that pay the cost of producing males while males do not spread their genes.

evolutionary biology↗

bioRxiv2017

Astral microtubule dynamics regulate anaphase * oscillation onset and set a robust final position * of the C. elegans zygote spindle.

During the asymmetric division of the Caenorhabditis elegans nematode zygote, the polarity cues distribution and daughter cell fates depend on the correct positioning of the mitotic spindle, which results from both centering and cortical pulling forces. Revealed by anaphase spindle rocking, these pulling forces are regulated by the force generator dynamics, which are in turn consequent of mitotic progression. We found a novel, additional, regulation of these forces by the spindle position. It controls astral microtubule availability at the cortex, on which the active force generators can pull. Importantly, this positional control relies on the polarity dependent LET-99 cortical band, which restricts or concentrates generators to a posterior crescent. After delaying anaphase onset, we detected this positional pulling force regulation in C. elegans as a precocious spindle rocking with respect to anaphase onset. We ascribed this control to the microtubule dynamics at the cortex. Indeed, in mapping the cortical contacts, we found a correlation between the centrosome-cortex distance and the microtubule contact density. In turn, it modulates pulling force generator activity. We modelled this control, predicting and experimentally validating that the posterior crescent extent controlled where the anaphase oscillations started, in addition to mitotic progression. We found in particular that the oscillation onset position resists changes in cellular geometry and moderate variations of active force generator count. Finally, we propose that spatially restricting force generator to a posterior crescent sets the spindles final position, reflecting polarity through the LET-99 dependent restriction of force generators to a posterior crescent. This regulation superimposes that of force generator processivity. This novel control confers a low dependence on microtubule and active force generator exact numbers or dynamics, provided that they exceed the threshold needed for posterior displacement. Interestingly, this robustness originates in cell mechanics rather than biochemical networks.

biophysics↗