Instituto Gulbenkian de Ciência, Oeiras, Portugal.
Instituto de Saúde Ambiental, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.
PLoS Biol. 2020 Mar 23;18(3):e3000663. doi: 10.1371/journal.pbio.3000663. eCollection 2020 Mar.
During in vitro fertilisation (IVF), pharmacological activation of the murine X chromosome-encoded receptor proteins Toll-like receptor (TLR) 7 and TLR8 reportedly results in male-biased litters by selectively disrupting the motility of X-bearing sperm cells. Thus-in the context of agonist treatment during IVF-these receptors act as 'suicidal' segregation distorters that impair their own transmission to the next generation. Such behaviour would, from an evolutionary perspective, be strongly selected against if present during natural fertilisation. Consequently, TLR7/8 biology in vivo must differ significantly from this in vitro situation to allow these genes to persist in the genome. Here, we use our current understanding of male germ cell biology and TLR function as a starting point to explore the mechanistic and evolutionary aspects of this apparent paradox.
在体外受精(IVF)过程中,据报道,通过药理学激活鼠 X 染色体编码的受体蛋白 Toll 样受体(TLR)7 和 TLR8,选择性地破坏携带 X 染色体的精子细胞的运动能力,可导致雄性偏向的后代。因此,在 IVF 过程中激动剂治疗的情况下,这些受体充当“自杀”分离干扰因子,损害其自身向后代的传递。如果在自然受精过程中存在这种行为,从进化的角度来看,这种行为将受到强烈的选择。因此,TLR7/8 的体内生物学必须与体外情况明显不同,以允许这些基因在基因组中存在。在这里,我们利用我们目前对雄性生殖细胞生物学和 TLR 功能的理解作为起点,探讨这一明显悖论的机制和进化方面。