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The Chrysosplenium sinicum genome provides insights into adaptive evolution of shade plants.

Authors :
Liu, Shuo
Wu, Zhihua
Yang, Tiange
Xu, Jindong
Aishan, Saimire
Qin, Erdai
Ma, Kang
Liu, Jiao
Qin, Rui
Wang, Jiangqing
Tie, Jun
Liu, Hong
Source :
Communications Biology. 8/16/2024, Vol. 7 Issue 1, p1-17. 17p.
Publication Year :
2024

Abstract

Chrysosplenium sinicum, a traditional Tibetan medicinal plant, can successfully thrive in low-light environments for long periods of time. To investigate the adaptive evolution of shade plants in low-light environments, we generated a chromosome-scale genome assembly (~320 Mb) for C. sinicum by combining PacBio sequencing and Hi-C technologies. Based on our results, gene families related to photosynthesis and cell respiration greatly expanded and evolved in C. sinicum genome due to intracellular DNA transfer from organelle genome to nuclear genome. Under positive selective pressure, adaptive evolution of light-harvesting complex II (LHCII) component protein CsLhcb1s resulted in the expansion of threonine residues at the phosphorylation site of STN7 kinase, potentially establishing a crucial genomic foundation for enhancing C. sinicum's adaptability in low-light environments. Through transcriptome and metabolome analysis, we identified chrysosplenol and chrysosplenoside as predominant flavonoid metabolites of C. sinicum and predicted their synthesis pathways. In addition, analysis of alternative splicing (AS) revealed that AS events help regulate state transition and flavonoid biosynthesis. The present study provides new insights into the genomes of shade plants exposed to low-light conditions and adaptive evolution of these genomes; in addition, the results improve our current knowledge on the biosynthetic and regulatory processes of chrysosplenol and chrysosplenoside. A chromosome-level genome assembly for Chrysosplenium sinicum combined with transcriptomic and metabolomic data provides insights into the adaptive evolution of shade plants as well as the pathways responsible for biosynthesis of chrysosplenol and chrysosplenoside. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23993642
Volume :
7
Issue :
1
Database :
Academic Search Index
Journal :
Communications Biology
Publication Type :
Academic Journal
Accession number :
179067737
Full Text :
https://doi.org/10.1038/s42003-024-06701-9