Department of Biological Sciences, Vanderbilt University, VU Station B 35-1634, Nashville, Tennessee 37235, USA.
Mycologia. 2010 Mar-Apr;102(2):269-78. doi: 10.3852/09-073.
Circadian rhythms are endogenous cellular patterns that associate multiple physiological and molecular functions with time. The Neurospora circadian system contains at least three oscillators: the FRQ/WC-dependent circadian oscillator (FWO), whose core components are the FRQ, WC-1, WC-2, FRH, and FWD-1 proteins; the WC-dependent circadian oscillator (WC-FLO); and one or more FRQ/ WC-independent oscillators (FLO). Little is known about the distribution of homologs of the Neurospora clock proteins or about the molecular foundations of circadian rhythms across fungi. Here, we examined 64 diverse fungal proteomes for homologs of all five Neurospora clock proteins and retraced their evolutionary history. The FRH and FWD-1 proteins were likely present in the fungal ancestor. WC-1 and WC-2 homologs are absent from the early diverging chytrids and Microsporidia but are present in all other major clades. In contrast to the deep origins of these four clock proteins FRQ homologs are taxonomically restricted within Sordariomycetes, Leotiomycetes and Dothideomycetes. The large number of FRH and FWD-1 homologs identified and their lack of concordance with the fungal species phylogeny indicate that they likely underwent multiple rounds of duplications and losses. In contrast, the FRQ, WC-1 and WC-2 proteins exhibit relatively few duplications and losses. A notable exception is the 10 FRQ-like proteins in Fusarium oxysporum, which resulted from nine duplication events. Our results suggest that the machinery required for FWO oscillator function is taxonomically restricted within Ascomycetes. Although the WC proteins are widely distributed, the functional diversity of the few non-Neurospora circadian oscillators suggests that a WC-FLO oscillator is unlikely to fully explain the observed rhythms. The contrast between the diversity of circadian oscillators and the conservation of most of their machinery is likely best explained by considering the centrality of noncircadian functions in which RNA helicase (FRH), F-box (FWD-1), WC-1 and WC-2 (light-sensing) proteins participate in fungi and eukaryotes.
昼夜节律是细胞内的固有模式,将多种生理和分子功能与时间联系起来。Neurospora 的生物钟系统至少包含三个振荡器:FRQ/WC 依赖性生物钟振荡器(FWO),其核心组件是 FRQ、WC-1、WC-2、FRH 和 FWD-1 蛋白;WC 依赖性生物钟振荡器(WC-FLO);和一个或多个 FRQ/WC 独立振荡器(FLO)。关于 Neurospora 时钟蛋白的同源物的分布或真菌中昼夜节律的分子基础知之甚少。在这里,我们检查了 64 种不同真菌的蛋白质组,寻找所有五个 Neurospora 时钟蛋白的同源物,并追溯了它们的进化历史。FRH 和 FWD-1 蛋白可能存在于真菌的祖先中。WC-1 和 WC-2 同源物不存在于早期分化的壶菌和微孢子虫中,但存在于所有其他主要的真菌分支中。与这四个时钟蛋白的深起源形成对比的是,FRQ 同源物在 Sordariomycetes、Leotiomycetes 和 Dothideomycetes 中是分类学上受限的。鉴定出的大量 FRH 和 FWD-1 同源物及其与真菌物种系统发育的不一致表明,它们可能经历了多次重复和丢失。相比之下,FRQ、WC-1 和 WC-2 蛋白的重复和丢失相对较少。一个值得注意的例外是在 Fusarium oxysporum 中发现的 10 个 FRQ 样蛋白,这是由九个复制事件产生的。我们的结果表明,FWO 振荡器功能所需的机制在子囊菌中是分类学上受限的。尽管 WC 蛋白广泛分布,但少数非 Neurospora 生物钟振荡器的功能多样性表明,WC-FLO 振荡器不太可能完全解释观察到的节律。昼夜节律振荡器的多样性与它们的大部分机制的保守性之间的对比,最好通过考虑 RNA 解旋酶(FRH)、F 框(FWD-1)、WC-1 和 WC-2(光感应)蛋白在真菌和真核生物中参与的非生物钟功能的中心性来解释。