TY - JOUR
T1 - Haplotype-resolved genome of diploid ginger (Zingiber officinale) and its unique gingerol biosynthetic pathway
AU - Li, Hong Lei
AU - Wu, Lin
AU - Dong, Zhaoming
AU - Jiang, Yusong
AU - Jiang, Sanjie
AU - Xing, Haitao
AU - Li, Qiang
AU - Liu, Guocheng
AU - Tian, Shuming
AU - Wu, Zhangyan
AU - Wu, Bin
AU - Li, Zhexin
AU - Zhao, Ping
AU - Zhang, Yan
AU - Tang, Jianmin
AU - Xu, Jiabao
AU - Huang, Ke
AU - Liu, Xia
AU - Zhang, Wenlin
AU - Liao, Qinhong
AU - Ren, Yun
AU - Huang, Xinzheng
AU - Li, Qingzhi
AU - Li, Chengyong
AU - Wang, Yi
AU - Xavier-Ravi, Baskaran
AU - Li, Honghai
AU - Liu, Yang
AU - Wan, Tao
AU - Liu, Qinhu
AU - Zou, Yong
AU - Jian, Jianbo
AU - Xia, Qingyou
AU - Liu, Yiqing
N1 - Publisher Copyright:
© The Author(s) 2021.
Funding Information:
This work was supported by funding from the Ginger Genome Project of Chongqing University of Arts and Sciences (2018), the Natural Science Foundation of Chongqing (cstc2019jcyj-msxmX0300, cstc2019jcyjmsxmX0697, CQYC201903201, cstc2019jscx-dxwtBX0028), the Foundation for High-level Talents of Chongqing University of Arts and Science (2017RTZ21, P2018TZ05), the Scientific and Technological Research Program of Chongqing Municipal Education Commission (KJZD-K202001304, KJQN201801339, KJQN201801330, KJQN201801335), the Foundation of Hubei Rural Science and Technology (2020BBA037), the State Key Research and Development Program of Hubei (2020BBA037) and the Foundation of Laiwu Experimental Station of the National Characteristic Vegetable Industry System. We thank J.Y. Yuan for the diagrammatic drawing of ginger. Z. Li, M. Sun, and J. Ye for help with material collection; D. Zhao, Z. Chen and P. Guo for additional help with UHPLC-MS/MS analysis; S. Zhang, T. Ma, and Z.D. Chen for comments on the evolution of ginger. We also thank Y. Liao, T. Zhang, and D. Lai for support of funding coordination.
PY - 2021/8/5
Y1 - 2021/8/5
N2 - Ginger (Zingiber officinale), the type species of Zingiberaceae, is one of the most widespread medicinal plants and spices. Here, we report a high-quality, chromosome-scale reference genome of ginger ‘Zhugen’, a traditionally cultivated ginger in Southwest China used as a fresh vegetable, assembled from PacBio long reads, Illumina short reads, and high-throughput chromosome conformation capture (Hi-C) reads. The ginger genome was phased into two haplotypes, haplotype 1 (1.53 Gb with a contig N50 of 4.68 M) and haplotype 0 (1.51 Gb with a contig N50 of 5.28 M). Homologous ginger chromosomes maintained excellent gene pair collinearity. In 17,226 pairs of allelic genes, 11.9% exhibited differential expression between alleles. Based on the results of ginger genome sequencing, transcriptome analysis, and metabolomic analysis, we proposed a backbone biosynthetic pathway of gingerol analogs, which consists of 12 enzymatic gene families, PAL, C4H, 4CL, CST, C3’H, C3OMT, CCOMT, CSE, PKS, AOR, DHN, and DHT. These analyses also identified the likely transcription factor networks that regulate the synthesis of gingerol analogs. Overall, this study serves as an excellent resource for further research on ginger biology and breeding, lays a foundation for a better understanding of ginger evolution, and presents an intact biosynthetic pathway for species-specific gingerol biosynthesis.
AB - Ginger (Zingiber officinale), the type species of Zingiberaceae, is one of the most widespread medicinal plants and spices. Here, we report a high-quality, chromosome-scale reference genome of ginger ‘Zhugen’, a traditionally cultivated ginger in Southwest China used as a fresh vegetable, assembled from PacBio long reads, Illumina short reads, and high-throughput chromosome conformation capture (Hi-C) reads. The ginger genome was phased into two haplotypes, haplotype 1 (1.53 Gb with a contig N50 of 4.68 M) and haplotype 0 (1.51 Gb with a contig N50 of 5.28 M). Homologous ginger chromosomes maintained excellent gene pair collinearity. In 17,226 pairs of allelic genes, 11.9% exhibited differential expression between alleles. Based on the results of ginger genome sequencing, transcriptome analysis, and metabolomic analysis, we proposed a backbone biosynthetic pathway of gingerol analogs, which consists of 12 enzymatic gene families, PAL, C4H, 4CL, CST, C3’H, C3OMT, CCOMT, CSE, PKS, AOR, DHN, and DHT. These analyses also identified the likely transcription factor networks that regulate the synthesis of gingerol analogs. Overall, this study serves as an excellent resource for further research on ginger biology and breeding, lays a foundation for a better understanding of ginger evolution, and presents an intact biosynthetic pathway for species-specific gingerol biosynthesis.
KW - Genome
KW - Genomics
KW - Horticultural plant genomes II
UR - https://doi.org/10.1038/s41438-021-00700-1
UR - https://www.scopus.com/pages/publications/85111955581
U2 - 10.1038/s41438-021-00627-7
DO - 10.1038/s41438-021-00627-7
M3 - Journal article
AN - SCOPUS:85111955581
SN - 2052-7276
VL - 8
JO - Horticulture Research
JF - Horticulture Research
M1 - 189
ER -