Aug 2026· PLoS Genetics· Vol 22, pp. e1012235 - e1012235· 0 citations· 86 references
Medicine
TL;DR
It is found that Rsp-derived small RNAs are underrepresented in driving testes of only one of the SD haplotypes, and this data imply that different haplotypes of complex drivers, like SD, can vary in their mechanism.
Abstract
Meiotic drivers achieve biased transmission to the next generation, often at the expense of their host. Drive is widespread and can shape the evolution of proteins, chromosome structure, and karyotypes. The sperm killer Segregation Distorter (SD) in Drosophila melanogaster is a well-studied driver but like most complex drivers, its mechanism remains elusive. SD is a multigene complex frequently associated with chromosomal inversions where the main driver locus, a truncated duplication of the gene RanGAP, kills wild-type sperm containing a satellite DNA called Responder (Rsp). Small RNAs are frequently implicated in the mechanisms of sperm killers, and we recently showed that Rsp is a source of small RNAs. Here we study the transcriptomes of two SD haplotypes and our results link Rsp expression and/or RNAs to drive. We found that Rsp-derived small RNAs are underrepresented in driving testes of only one of the SD haplotypes. We show that over-expressing Rsp is sufficient to reduce drive strength in the haplotype with downregulated Rsp but not the other. We therefore shed light on the mechanism of SD by making a connection between the target and the drive phenotype. Additionally, our data imply that different haplotypes of complex drivers, like SD, can vary in their mechanism.
The t-haplotype is a selfish variant of the mouse chromosome 17. It reaches 90-100% transmission rates in heterozygous (+/t) males through a poison-antidote system that disables sperm carrying the homologous (+) haplotype. While several poisons and one antidote have been identified, how these mediate drive, and what ad...
Reka K. Kelemen, A. Lindholm, Beatriz Viçoso· bioRxiv· 0 citations
ABSTRACT Transposable elements (TEs) are widespread genomic parasites, whose activity is largely restrained by RNA interference pathways. Some of these pathways also contribute to antiviral immunity, allowing a mechanistic overlap that could generate interactions—or even trade-offs—between TE repression and viral defen...
Camille Mayeux, Chloé Garambois, A. Larue et al.· Journal of Virology· 0 citations
DNA double-strand breaks (DSBs) are toxic lesions that must be repaired to avoid genetic loss and genome rearrangements. Various conserved pathways are involved in DSB repair, producing different outcomes. Accumulating evidence has identified RNA, particularly small RNAs as a new player in DSB repair. DSB-induced small...
Etienne Mochet, C. White, Jérémy Verbeke et al.· bioRxiv· 0 citations
Many animal species replace histones with protamines during spermatogenesis. Although essential for sperm function, protamines evolve rapidly for reasons that remain unknown. Using in vivo gene replacement, we examined the causes and consequences of the rapid evolution of Mst77F, a protamine essential for male fertilit...
Ching-Ho Chang, A. de la Cruz, Hung-Yu Lai et al.· Science Advances· 0 citations
Meiotic drivers are selfish elements that co-opt gametogenesis to increase their own transmission. Driving alleles may spread in a population even if harmful to overall fitness, requiring the emergence of host suppressors to ameliorate these costs. In some cases, intense coevolutionary arms races between drivers and th...
In many organisms, meiotic crossover recombination is suppressed near the extreme ends of chromosomes. Here, we show that multiple, often chromosome-specific, suppressive mechanisms with differing ranges contribute to the consistently low enrichment of recombination-promoting axis proteins and the downregulation of DNA...
A. Raghavan, K. May, Vijayalakshmi V. Subramanian et al.· eLife· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.