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Ridges, J. T.

Publications and source records attributed to Ridges, J. T..

2 recordsLinked to original sources

Drive, suppression, and escape from suppression of a selfish chromosome

Meiotic drivers are selfish chromosomes that are predicted to spark a rapid intragenomic arms-race with their suppressors. However, the long-term persistence of unsuppressed selfish chromosomes in natural populations violates these theoretical expectations. The Drosophila pseudoobscura Sex-Ratio (SR) chromosome exemplifies this problem, sometimes referred to as the "ancient gene drive paradox". Here, we reconstruct the evolutionary history of this SR chromosome and show that its genetic architecture and complexity has been shaped by a history of drive, suppression, and escape from suppression. Our results indicate that the current lack of resistance to the SR chromosome represents a transient condition awaiting the emergence of new suppressors. SIGNIFICANCEIntragenomic arms races triggered by selfish chromosomes are expected to drive rapid evolution through cycles of drive, suppression, and escape from suppression. Despite these expectations, some selfish chromosomes such as the D. pseudoobscura Sex-Ratio (SR) chromosome exist unsuppressed for extended periods of time. Despite the absence of suppression, we uncover currently segregating suppressors against the ancestral version and evidence of recent dynamic evolution on the SR chromosome. Todays SR chromosome thus represents a transient state in a surprisingly slow arms race. Taken together, the lack of suppressors against this selfish chromosome can be explained by mutational limits for the emergence of suppressors.

evolutionary biology↗

Overdrive is essential for targeted sperm elimination by Segregation Distorter

Intra-genomic conflict driven by selfish chromosomes is a powerful force that shapes the evolution of genomes and species. In the male germline, many selfish chromosomes bias transmission in their own favor by eliminating spermatids bearing the competing homologous chromosomes. However, the mechanisms of targeted gamete elimination remain mysterious. Here, we show that Overdrive (Ovd), a gene required for both segregation distortion and male sterility in Drosophila pseudoobscura hybrids, is broadly conserved in Dipteran insects but dispensable for viability and fertility. In D. melanogaster, Ovd is required for targeted Responder spermatid elimination after the histone-to-protamine transition in the classical Segregation Distorter system. We propose that Ovd functions as a general spermatid quality checkpoint that is hijacked by independent selfish chromosomes to eliminate competing gametes.

genetics↗