State Key Laboratory of Genetic Engineering and Collaborative Innovation Center of Genetics and Development, Ministry of Education Key Laboratory of Biodiversity and Ecological Engineering, Institute of Plant Biology, Center of Evolutionary Biology, School of Life Sciences, Fudan University, 2005 Songhu Road, Shanghai 200433, China; Department of Biology, The Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA 16802, USA.
Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Lanhei Road, Kunming 650201, China.
Mol Plant. 2021 May 3;14(5):748-773. doi: 10.1016/j.molp.2021.02.006. Epub 2021 Feb 22.
Fabaceae are the third largest angiosperm family, with 765 genera and ∼19 500 species. They are important both economically and ecologically, and global Fabaceae crops are intensively studied in part for their nitrogen-fixing ability. However, resolution of the intrasubfamilial Fabaceae phylogeny and divergence times has remained elusive, precluding a reconstruction of the evolutionary history of symbiotic nitrogen fixation in Fabaceae. Here, we report a highly resolved phylogeny using >1500 nuclear genes from newly sequenced transcriptomes and genomes of 391 species, along with other datasets, for a total of 463 legumes spanning all 6 subfamilies and 333 of 765 genera. The subfamilies are maximally supported as monophyletic. The clade comprising subfamilies Cercidoideae and Detarioideae is sister to the remaining legumes, and Duparquetioideae and Dialioideae are successive sisters to the clade of Papilionoideae and Caesalpinioideae. Molecular clock estimation revealed an early radiation of subfamilies near the K/Pg boundary, marked by mass extinction, and subsequent divergence of most tribe-level clades within ∼15 million years. Phylogenomic analyses of thousands of gene families support 28 proposed putative whole-genome duplication/whole-genome triplication events across Fabaceae, including those at the ancestors of Fabaceae and five of the subfamilies, and further analyses supported the Fabaceae ancestral polyploidy. The evolution of rhizobial nitrogen-fixing nodulation in Fabaceae was probed by ancestral character reconstruction and phylogenetic analyses of related gene families and the results support the hypotheses of one or two switch(es) to rhizobial nodulation followed by multiple losses. Collectively, these results provide a foundation for further morphological and functional evolutionary analyses across Fabaceae.
豆科是被子植物的第三大科,包含 765 属和约 19,500 个物种。它们在经济和生态上都很重要,全球的豆科作物因其固氮能力而受到广泛研究。然而,豆科亚科内的系统发育关系和分歧时间仍然难以解决,这使得豆科共生固氮的进化历史无法重建。在这里,我们利用来自 391 种新测序转录组和基因组的>1500 个核基因以及其他数据集报告了一个高度解析的系统发育关系,总共涵盖了 6 个亚科的 463 种豆科植物和 765 属中的 333 属。亚科被最大程度地支持为单系。包含 Cercidoideae 和 Detarioideae 亚科的分支与其余豆科植物为姐妹关系,而 Duparquetioideae 和 Dialioideae 是 Papilionoideae 和 Caesalpinioideae 分支的连续姐妹关系。分子钟估计表明,在 K/Pg 边界附近,亚科发生了早期辐射,标志着大规模灭绝,随后在大约 1500 万年的时间里,大多数部落级分支发生了分歧。对数千个基因家族的系统基因组分析支持了豆科植物中 28 个推测的全基因组加倍/全基因组三倍事件,包括豆科植物和 5 个亚科的祖先,进一步的分析支持了豆科植物的祖先多倍体。通过对相关基因家族的祖先特征重建和系统发育分析,探讨了豆科植物根瘤菌固氮结瘤的进化,结果支持了一个或两个向根瘤菌结瘤的转变,然后是多次丢失的假说。总的来说,这些结果为豆科植物的进一步形态和功能进化分析提供了基础。