Centre for Infectious Diseases, Parasitology, Heidelberg University Hospital, Heidelberg, Germany.
Graduate Program in Areas of Basic and Applied Biology, Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Porto, Portugal.
Front Cell Infect Microbiol. 2021 Apr 9;11:660679. doi: 10.3389/fcimb.2021.660679. eCollection 2021.
, the unicellular parasite that causes malaria, evolved a highly unusual mode of reproduction. During its complex life cycle, invasive or transmissive stages alternate with proliferating stages, where a single parasite can produce tens of thousands of progeny. In the clinically relevant blood stage of infection, the parasite replicates its genome up to thirty times and forms a multinucleated cell before daughter cells are assembled. Thus, within a single cell cycle, develops from a haploid to a polypoid cell, harboring multiple copies of its genome. Polyploidy creates several biological challenges, such as imbalances in genome output, and cells can respond to this by changing their size and/or alter the production of RNA species and protein to achieve expression homeostasis. However, the effects and possible adaptations of to the massively increasing DNA content are unknown. Here, we revisit and embed current literature in the context of polyploidy and propose potential mechanisms of the parasite to cope with the increasing gene dosage.
疟原虫是一种单细胞寄生虫,它进化出了一种非常特殊的繁殖方式。在其复杂的生命周期中,侵袭性或传染性阶段与增殖阶段交替出现,在增殖阶段,一个寄生虫可以产生成千上万的后代。在临床上相关的感染血阶段,寄生虫的基因组可以复制多达三十次,并在形成多核细胞后再组装成子细胞。因此,在一个细胞周期内,疟原虫从单倍体发育成多倍体细胞,携带其基因组的多个拷贝。多倍体化会带来一些生物学挑战,例如基因组输出的失衡,细胞可以通过改变其大小和/或改变 RNA 种类和蛋白质的产生来应对这种情况,以实现表达平衡。然而,疟原虫对大量增加的 DNA 含量的影响和可能的适应机制尚不清楚。在这里,我们重新审视并将当前的疟原虫文献置于多倍体的背景下,并提出寄生虫可能应对基因剂量不断增加的潜在机制。