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The Cardamine enshiensis genome reveals whole genome duplication and insight into selenium hyperaccumulation and tolerance

Authors :
Chuying Huang
Hongqin Ying
Xibiao Yang
Yuan Gao
Tuo Li
Bo Wu
Meng Ren
Zixiong Zhang
Jun Ding
Jianhua Gao
Dan Wen
Xingzhi Ye
Ling Liu
Huan Wang
Guogen Sun
Yi Zou
Nansheng Chen
Li Wang
Source :
Cell Discovery, Vol 7, Iss 1, Pp 1-14 (2021)
Publication Year :
2021
Publisher :
Nature Publishing Group, 2021.

Abstract

Abstract Cardamine enshiensis is a well-known selenium (Se)-hyperaccumulating plant. Se is an essential trace element associated with many health benefits. Despite its critical importance, genomic information of this species is limited. Here, we report a chromosome-level genome assembly of C. enshiensis, which consists of 443.4 Mb in 16 chromosomes with a scaffold N50 of 24 Mb. To elucidate the mechanism of Se tolerance and hyperaccumulation in C. enshiensis, we generated and analyzed a dataset encompassing genomes, transcriptomes, and metabolomes. The results reveal that flavonoid, glutathione, and lignin biosynthetic pathways may play important roles in protecting C. enshiensis from stress induced by Se. Hi-C analysis of chromatin interaction patterns showed that the chromatin of C. enshiensis is partitioned into A and B compartments, and strong interactions between the two telomeres of each chromosome were correlated with histone modifications, epigenetic markers, DNA methylation, and RNA abundance. Se supplementation could affect the 3D chromatin architecture of C. enshiensis at the compartment level. Genes with compartment changes after Se treatment were involved in selenocompound metabolism, and genes in regions with topologically associated domain insulation participated in cellular responses to Se, Se binding, and flavonoid biosynthesis. This multiomics research provides molecular insight into the mechanism underlying Se tolerance and hyperaccumulation in C. enshiensis.

Subjects

Subjects :
Cytology
QH573-671

Details

Language :
English
ISSN :
20565968
Volume :
7
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Cell Discovery
Publication Type :
Academic Journal
Accession number :
edsdoj.0c143aa9dc424db38b9e87d65d2008d1
Document Type :
article
Full Text :
https://doi.org/10.1038/s41421-021-00286-x