The Apostasia Genome and the Evolution of Orchids
There are amendments to this paper OPEN LETTER doi:10.1038/nature23897 The Apostasia genome and the evolution of orchids Guo-Qiang Zhang1*, Ke-Wei Liu1*, Zhen Li2,3*, Rolf Lohaus2,3*, Yu-Yun Hsiao4,5*, Shan-Ce Niu1,6, Jie-Yu Wang1,7, Yao-Cheng Lin2,3†, Qing Xu1, Li-Jun Chen1, Kouki Yoshida8, Sumire Fujiwara9, Zhi-Wen Wang10, Yong-Qiang Zhang1, Nobutaka Mitsuda9, Meina Wang1, Guo-Hui Liu1, Lorenzo Pecoraro1, Hui-Xia Huang1, Xin-Ju Xiao1, Min Lin1, Xin-Yi Wu1, Wan-Lin Wu1,4, You-Yi Chen4,5, Song-Bin Chang4,5, Shingo Sakamoto9, Masaru Ohme-Takagi9,11, Masafumi Yagi12, Si-Jin Zeng1,7, Ching-Yu Shen13, Chuan-Ming Yeh11, Yi-Bo Luo6, Wen-Chieh Tsai4,5,13, Yves Van de Peer2,3,14 & Zhong-Jian Liu1,7,15,16 Constituting approximately 10% of flowering plant species, orchids those of other Orchidaceae subfamilies, which have three sepals, three (Orchidaceae) display unique flower morphologies, possess an petals (of which one has specialized to form the labellum), and stamens extraordinary diversity in lifestyle, and have successfully colonized and pistil fused into a more complex gynostemium (Extended Data almost every habitat on Earth1–3. Here we report the draft genome Fig. 1b), but are similar to those of some species of Hypoxidaceae sequence of Apostasia shenzhenica4, a representative of one of two (a sister family to Orchidaceae, in the order Asparagales). genera that form a sister lineage to the rest of the Orchidaceae, We sequenced the A. shenzhenica genome using a combination providing a reference for inferring the genome content and of different approaches; the total length of the final assembly was structure of the most recent common ancestor of all extant orchids 349 Mb (see Methods and Supplementary Tables 1–4).
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