Department of Biology, University of Texas at Arlington, Arlington, TX, 76019, USA.
Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 75235, USA.
Heredity (Edinb). 2023 Aug;131(2):119-129. doi: 10.1038/s41437-023-00628-3. Epub 2023 Jun 6.
Despite the presence of obligately parthenogenetic (OP) lineages derived from sexual ancestors in diverse phylogenetic groups, the genetic mechanisms giving rise to the OP lineages remain poorly understood. The freshwater microcrustacean Daphnia pulex typically reproduces via cyclical parthenogenesis. However, some populations of OP D. pulex have emerged due to ancestral hybridization and introgression events between two cyclically parthenogenetic (CP) species D. pulex and D. pulicaria. These OP hybrids produce both subitaneous and resting eggs parthenogenetically, deviating from CP isolates where resting eggs are produced via conventional meiosis and mating. This study examines the genome-wide expression and alternative splicing patterns of early subitaneous versus early resting egg production in OP D. pulex isolates to gain insight into the genes and mechanisms underlying this transition to obligate parthenogenesis. Our differential expression and functional enrichment analyses revealed a downregulation of meiosis and cell cycle genes during early resting egg production, as well as divergent expression patterns of metabolism, biosynthesis, and signaling pathways between the two reproductive modes. These results provide important gene candidates for future experimental verification, including the CDC20 gene that activates the anaphase-promoting complex in meiosis.
尽管在不同的进化群中存在源自有性祖先的专性孤雌生殖(OP)谱系,但导致 OP 谱系产生的遗传机制仍知之甚少。淡水小型甲壳动物 Daphnia pulex 通常通过周期性孤雌生殖进行繁殖。然而,由于两个周期性孤雌生殖(CP)物种 D. pulex 和 D. pulicaria 之间的祖先杂交和基因渗入事件,一些 OP D. pulex 种群已经出现。这些 OP 杂种既能孤雌生殖产生突发卵,也能孤雌生殖产生休眠卵,与通过传统减数分裂和交配产生休眠卵的 CP 分离株不同。本研究通过比较 OP D. pulex 分离株早期突发卵和早期休眠卵的全基因组表达和可变剪接模式,深入了解这种向专性孤雌生殖的转变的基因和机制。我们的差异表达和功能富集分析表明,在早期休眠卵产生过程中,减数分裂和细胞周期基因下调,两种生殖方式之间的代谢、生物合成和信号通路的表达模式也存在差异。这些结果为未来的实验验证提供了重要的候选基因,包括在减数分裂中激活后期促进复合物的 CDC20 基因。