Department of Plant Sciences, Laboratory of Genetics, Wageningen University, Wageningen, The Netherlands.
Microbiol Mol Biol Rev. 2023 Sep 26;87(3):e0002221. doi: 10.1128/mmbr.00022-21. Epub 2023 Jul 6.
This paper addresses the stability of mycelial growth in fungi and differences between ascomycetes and basidiomycetes. Starting with general evolutionary theories of multicellularity and the role of sex, we then discuss individuality in fungi. Recent research has demonstrated the deleterious consequences of nucleus-level selection in fungal mycelia, favoring cheaters with a nucleus-level benefit during spore formation but a negative effect on mycelium-level fitness. Cheaters appear to generally be loss-of-fusion (LOF) mutants, with a higher propensity to form aerial hyphae developing into asexual spores. Since LOF mutants rely on heterokaryosis with wild-type nuclei, we argue that regular single-spore bottlenecks can efficiently select against such cheater mutants. We then zoom in on ecological differences between ascomycetes being typically fast-growing but short-lived with frequent asexual-spore bottlenecks and basidiomycetes being generally slow-growing but long-lived and usually without asexual-spore bottlenecks. We argue that these life history differences have coevolved with stricter nuclear quality checks in basidiomycetes. Specifically, we propose a new function for clamp connections, structures formed during the sexual stage in ascomycetes and basidiomycetes but during somatic growth only in basidiomycete dikaryons. During dikaryon cell division, the two haploid nuclei temporarily enter a monokaryotic phase, by alternatingly entering a retrograde-growing clamp cell, which subsequently fuses with the subapical cell to recover the dikaryotic cell. We hypothesize that clamp connections act as screening devices for nuclear quality, with both nuclei continuously testing each other for fusion ability, a test that LOF mutants will fail. By linking differences in longevity of the mycelial phase to ecology and stringency of nuclear quality checks, we propose that mycelia have a constant and low lifetime cheating risk, irrespective of their size and longevity.
本文探讨了真菌菌丝生长的稳定性以及子囊菌和担子菌之间的差异。首先从多细胞生物的一般进化理论和性别的作用出发,然后讨论了真菌的个体性。最近的研究表明,在真菌菌丝中核水平选择具有破坏性后果,有利于在孢子形成过程中具有核水平优势的骗子,但对菌丝水平适应性有负面影响。骗子似乎通常是融合丢失(LOF)突变体,更有可能形成气生菌丝并发育成无性孢子。由于 LOF 突变体依赖于具有野生型核的异核作用,我们认为常规的单孢子瓶颈可以有效地选择对抗这种骗子突变体。然后,我们放大了子囊菌和担子菌之间的生态差异,子囊菌通常生长迅速但寿命短,经常经历无性孢子瓶颈,担子菌通常生长缓慢但寿命长,通常没有无性孢子瓶颈。我们认为这些生活史差异与担子菌中更严格的核质量检查共同进化。具体来说,我们提出了夹点连接的新功能,夹点连接在子囊菌和担子菌的有性阶段形成,但仅在担子菌双核体的体细胞生长中形成。在双核体细胞分裂期间,两个单倍体核暂时进入单核期,通过交替进入逆行生长的夹点细胞,随后与亚顶细胞融合,恢复双核细胞。我们假设夹点连接作为核质量的筛选装置,两个核不断相互测试融合能力,LOF 突变体将无法通过测试。通过将菌丝阶段的寿命差异与生态学和核质量检查的严格性联系起来,我们提出无论菌丝的大小和寿命如何,菌丝都具有恒定且低的终生欺骗风险。