Lu Zhigang, Spänig Sebastian, Weth Oliver, Grevelding Christoph G
Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Insitute for Parasitology, BFS, Justus Liebig University Giessen, Giessen, Germany.
Front Genet. 2019 Sep 6;10:796. doi: 10.3389/fgene.2019.00796. eCollection 2019.
Schistosomes are the only platyhelminths that have evolved separate sexes, and they exhibit a unique reproductive biology because the female's sexual maturation depends on a constant pairing contact with the male. In the female, pairing leads to gonad differentiation, which is associated with substantial morphological changes, and controls among others the expression of gonad-associated genes. In the male, no morphological changes have been observed after pairing, although first data indicated an effect of pairing on gene transcription. Comprehensive transcriptomic approaches have revealed an unexpected high number of genes that are differentially transcribed in the male after pairing. Their identities suggest roles for the male that are not restricted to feeding and enhanced muscular power to transport paired female and, as assumed before, to induce its sexual maturation by one "magic" factor. Instead, a more complex picture emerges in which both partners live in a reciprocal sender-recipient relationship that not only affects the gonads of both genders but may also involve tactile stimuli, transforming growth factor β signaling, nutritional parts, and neuronal processes, including neuropeptides and G protein-coupled receptor signaling. This review provides a summary of transcriptomics including an overview of genes expressed in a pairing-dependent manner in schistosome males. This may stimulate further research in understanding the role of the male as the recipient of the female's signals upon pairing, the male's "capacitation," and its subsequent competence as a sender of information. The latter process finally transforms a sexually immature, autonomous female without completely developed gonads into a sexually mature, partially non-autonomous female with fully differentiated gonads and enormous egg production capacity.
血吸虫是唯一进化出雌雄异体的扁形虫,它们表现出独特的生殖生物学特性,因为雌性的性成熟依赖于与雄性持续的配对接触。在雌性中,配对会导致性腺分化,这与显著的形态变化相关,并且在其他方面控制着性腺相关基因的表达。在雄性中,配对后未观察到形态变化,尽管初步数据表明配对对基因转录有影响。综合转录组学方法揭示了配对后雄性中差异转录的基因数量出乎意料地多。它们的特性表明雄性的作用不仅限于进食和增强运送配对雌性的肌肉力量,以及如之前所假设的通过一个“神奇”因子诱导其性成熟。相反,出现了一幅更复杂的图景,即双方处于相互的信号发送者 - 接收者关系中,这不仅影响两性的性腺,还可能涉及触觉刺激、转化生长因子β信号传导、营养成分以及神经过程,包括神经肽和G蛋白偶联受体信号传导。本综述总结了转录组学,包括血吸虫雄性中以配对依赖方式表达的基因概述。这可能会刺激进一步的研究,以了解雄性在配对时作为雌性信号接收者的作用、雄性的“获能”以及其随后作为信息发送者的能力。后一过程最终将一个性未成熟、自主的雌性,其性腺未完全发育,转变为一个性成熟、部分非自主的雌性,其性腺完全分化且具有巨大的产卵能力。