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基于三种不同分子钟模型估计的卵菌进化的多位点时标。

A multilocus timescale for oomycete evolution estimated under three distinct molecular clock models.

机构信息

Department of Biology, Franklin & Marshall College, Lancaster, PA, USA.

出版信息

BMC Evol Biol. 2014 May 12;14:101. doi: 10.1186/1471-2148-14-101.

Abstract

BACKGROUND

Molecular clock methodologies allow for the estimation of divergence times across a variety of organisms; this can be particularly useful for groups lacking robust fossil histories, such as microbial eukaryotes with few distinguishing morphological traits. Here we have used a Bayesian molecular clock method under three distinct clock models to estimate divergence times within oomycetes, a group of fungal-like eukaryotes that are ubiquitous in the environment and include a number of devastating pathogenic species. The earliest fossil evidence for oomycetes comes from the Lower Devonian (~400 Ma), however the taxonomic affinities of these fossils are unclear.

RESULTS

Complete genome sequences were used to identify orthologous proteins among oomycetes, diatoms, and a brown alga, with a focus on conserved regulators of gene expression such as DNA and histone modifiers and transcription factors. Our molecular clock estimates place the origin of oomycetes by at least the mid-Paleozoic (430-400 Ma), with the divergence between two major lineages, the peronosporaleans and saprolegnialeans, in the early Mesozoic (225-190 Ma). Divergence times estimated under the three clock models were similar, although only the strict and random local clock models produced reliable estimates for most parameters.

CONCLUSIONS

Our molecular timescale suggests that modern pathogenic oomycetes diverged well after the origin of their respective hosts, indicating that environmental conditions or perhaps horizontal gene transfer events, rather than host availability, may have driven lineage diversification. Our findings also suggest that the last common ancestor of oomycetes possessed a full complement of eukaryotic regulatory proteins, including those involved in histone modification, RNA interference, and tRNA and rRNA methylation; interestingly no match to canonical DNA methyltransferases could be identified in the oomycete genomes studied here.

摘要

背景

分子钟方法允许对各种生物体的分歧时间进行估计;对于缺乏可靠化石历史的群体,例如具有少数形态特征的微生物真核生物,这可能特别有用。在这里,我们使用了三种不同的钟模型下的贝叶斯分子钟方法来估计卵菌的分歧时间,卵菌是一类真菌样真核生物,在环境中无处不在,包括一些具有破坏性的致病物种。卵菌最早的化石证据来自下泥盆纪(约 4 亿年前),然而这些化石的分类学亲缘关系尚不清楚。

结果

使用完整的基因组序列在卵菌、硅藻和一种褐藻中鉴定了同源蛋白,重点是保守的基因表达调控因子,如 DNA 和组蛋白修饰酶以及转录因子。我们的分子钟估计将卵菌的起源至少置于古生代中期(约 4.3 亿至 4 亿年前),两个主要谱系,即卵孢子菌和腐霉菌的分歧发生在中生代早期(约 2.25 亿至 1.9 亿年前)。虽然只有严格和随机局部钟模型为大多数参数产生了可靠的估计,但三种钟模型估计的分歧时间相似。

结论

我们的分子时间尺度表明,现代致病性卵菌在其各自宿主起源后才分化出来,这表明环境条件或可能是水平基因转移事件而不是宿主可用性可能推动了谱系多样化。我们的研究结果还表明,卵菌的最后共同祖先拥有完整的真核生物调控蛋白,包括参与组蛋白修饰、RNA 干扰以及 tRNA 和 rRNA 甲基化的蛋白;有趣的是,在研究的卵菌基因组中未发现典型的 DNA 甲基转移酶的匹配物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5e2/4030286/7c5d4c1dd4f7/1471-2148-14-101-1.jpg

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