Login / Signup

Comparing genomes of Fructus Amomi-producing species reveals genetic basis of volatile terpenoid divergence.

Peng YangXu-Yi LingXiao-Fan ZhouYuan-Xia ChenTian-Tian WangXiao-Jing LinYuan-Yuan ZhaoYu-Shi YeLin-Xuan HuangYe-Wen SunYu-Xin QiDong-Ming MaRuo-Ting ZhanXue-Shuang HuangJin-Fen Yang
Published in: Plant physiology (2023)
Wurfbainia longiligularis and Wurfbainia villosa are both rich in volatile terpenoids and are two primary plant sources of Fructus Amomi used for curing gastrointestinal diseases. Metabolomic profiling has demonstrated that bornyl diphosphate (BPP)-related terpenoids are more abundant in the W. villosa seeds and have a wider tissue distribution in W. longiligularis. To explore the genetic mechanisms underlying the volatile terpenoids divergence, a high-quality chromosome-level genome of W. longiligularis (2.29 Gb, contig N50 of 80.39 Mb) was assembled. Functional characterization of 17 terpene synthases (WlTPSs) revealed that WlBPPS, along with WlTPS 24/26/28 with bornyl diphosphate synthase (BPPS) activity, contribute to the wider tissue distribution of BPP-related terpenoids in W. longiligularis compared to W. villosa. Furthermore, transgenic Nicotiana tabacum showed that the GCN4-motif element positively regulates seed expression of WvBPPS and thus promotes the enrichment of BPP-related terpenoids in W. villosa seeds. Systematic identification and analysis of candidate TPS in 29 monocot plants from 16 families indicated that substantial expansion of TPS-a and TPS-b subfamily genes in Zingiberaceae may have driven increased diversity and production of volatile terpenoids. Evolutionary analysis and functional identification of BPPS genes showed that BPP-related terpenoids may be distributed only in the Zingiberaceae of monocot plants. This research provides valuable genomic resources for breeding and improving Fructus Amomi with medicinal and edible value and sheds light on the evolution of terpenoid biosynthesis in Zingiberaceae.
Keyphrases
  • genome wide
  • dna methylation
  • gas chromatography
  • single cell
  • gene expression
  • mass spectrometry
  • drinking water
  • genome wide identification
  • binding protein