Wallen R M, Perlin Michael H
Department of Biology, University of Louisville, Louisville, KY, United States.
Front Microbiol. 2018 Mar 21;9:503. doi: 10.3389/fmicb.2018.00503. eCollection 2018.
Sexual reproduction likely evolved as protection from environmental stresses, specifically, to repair DNA damage, often via homologous recombination. In higher eukaryotes, meiosis and the production of gametes with allelic combinations different from parental type provides the side effect of increased genetic variation. In fungi it appears that while the maintenance of meiosis is paramount for success, outcrossing is not a driving force. In the subkingdom , fungal members are characterized by existence of a dikaryon for extended stages within the life cycle. Such fungi possess functional or, in some cases, relictual, loci that govern sexual reproduction between members of their own species. All mating systems identified so far in the employ a pheromone/receptor system for haploid organisms to recognize a compatible mating partner, although the paradigm in the Ascomycota, e.g., , is that genes for the pheromone precursor and receptor are not found in the mating-type locus but rather are regulated by its products. Similarly, the mating systems in the Ascomycota are bipolar, with two non-allelic idiomorphs expressed in cells of opposite mating type. In contrast, for the Basidiomycota, both bipolar and tetrapolar mating systems have been well characterized; further, at least one locus directly encodes the pheromone precursor and the receptor for the pheromone of a different mating type, while a separate locus encodes proteins that may regulate the first locus and/or additional genes required for downstream events. Heterozygosity at both of two unlinked loci is required for cells to productively mate in tetrapolar systems, whereas in bipolar systems the two loci are tightly linked. Finally, a trade-off exists in wild fungal populations between sexual reproduction and the associated costs, with adverse conditions leading to mating. For fungal mammal pathogens, the products of sexual reproduction can be targets for the host immune system. The opposite appears true for phytopathogenic fungi, where mating and pathogenicity are inextricably linked. Here, we explore, compare, and contrast different strategies used among the , both saprophytic and pathogenic fungi, and highlight differences between pathogens of mammals and pathogens of plants, providing context for selective pressures acting on this interesting group of fungi.
有性生殖可能是作为对环境压力的一种保护机制而进化的,具体而言,是为了修复DNA损伤,通常是通过同源重组来实现。在高等真核生物中,减数分裂以及产生具有与亲本类型不同的等位基因组合的配子会带来遗传变异增加的副作用。在真菌中,虽然减数分裂的维持对于成功至关重要,但异交并不是驱动力。在真菌亚界中,真菌成员的特征是在生命周期的延长阶段存在双核体。这类真菌拥有控制其自身物种成员之间有性生殖的功能性位点,在某些情况下是残余位点。到目前为止,在真菌中鉴定出的所有交配系统都采用信息素/受体系统,使单倍体生物体能够识别兼容的交配伙伴,尽管子囊菌门(例如酿酒酵母)的模式是,信息素前体和受体的基因不在交配型位点中,而是由其产物调控。同样,子囊菌门中的交配系统是两极的,在相反交配型的细胞中表达两种非等位的特异形式。相比之下,对于担子菌门,两极和四极交配系统都已得到很好的表征;此外,至少一个位点直接编码不同交配型信息素的前体和受体,而另一个单独的位点编码可能调控第一个位点和/或下游事件所需的其他基因的蛋白质。在四极系统中,细胞进行有效交配需要两个不连锁位点的杂合性,而在两极系统中,这两个位点紧密连锁。最后,在野生真菌种群中,有性生殖与其相关成本之间存在权衡,不利条件会导致交配。对于真菌性哺乳动物病原体,有性生殖的产物可能成为宿主免疫系统的靶标。对于植物病原真菌,情况似乎相反,交配和致病性紧密相连。在这里,我们探索、比较和对比了真菌(包括腐生真菌和病原真菌)中使用的不同策略,并突出了哺乳动物病原体和植物病原体之间的差异,为作用于这一有趣真菌群体的选择压力提供背景。