The genome of a wild Medicago species provides insights into the tolerant mechanisms of legume forage to environmental stress

Tianzuo Wang(Chinese Academy of Sciences), Lifei Ren(Chinese Academy of Sciences), Caihong Li(Chinese Academy of Sciences), Di Zhang(Chinese Academy of Sciences), Xiuxiu Zhang(Chinese Academy of Sciences), Gang Zhou(Novogene Bioinformatics Institute), Dan Gao(Novogene Bioinformatics Institute), Rujin Chen(Lanzhou University), Yuhui Chen(Lanzhou University), Zhaolan Wang(Chinese Academy of Agricultural Sciences), Fengling Shi(Inner Mongolia Agricultural University), Andrew Farmer(National Center for Genome Resources), Yansu Li(Institute of Vegetables and Flowers), Mengyan Zhou(Novogene Bioinformatics Institute), Nevin D. Young(University of Minnesota), Wenhao Zhang(Chinese Academy of Sciences)
BMC Biology
May 6, 2021
Cited by 89Open Access
Full Text

Abstract

BACKGROUND: Medicago ruthenica, a wild and perennial legume forage widely distributed in semi-arid grasslands, is distinguished by its outstanding tolerance to environmental stress. It is a close relative of commonly cultivated forage of alfalfa (Medicago sativa). The high tolerance of M. ruthenica to environmental stress makes this species a valuable genetic resource for understanding and improving traits associated with tolerance to harsh environments. RESULTS: We sequenced and assembled genome of M. ruthenica using an integrated approach, including PacBio, Illumina, 10×Genomics, and Hi-C. The assembled genome was 904.13 Mb with scaffold N50 of 99.39 Mb, and 50,162 protein-coding genes were annotated. Comparative genomics and transcriptomic analyses were used to elucidate mechanisms underlying its tolerance to environmental stress. The expanded FHY3/FAR1 family was identified to be involved in tolerance of M. ruthenica to drought stress. Many genes involved in tolerance to abiotic stress were retained in M. ruthenica compared to other cultivated Medicago species. Hundreds of candidate genes associated with drought tolerance were identified by analyzing variations in single nucleotide polymorphism using accessions of M. ruthenica with varying tolerance to drought. Transcriptomic data demonstrated the involvements of genes related to transcriptional regulation, stress response, and metabolic regulation in tolerance of M. ruthenica. CONCLUSIONS: We present a high-quality genome assembly and identification of drought-related genes in the wild species of M. ruthenica, providing a valuable resource for genomic studies on perennial legume forages.


Related Papers

No related papers found

Powered by citation graph analysis