4.7 Article

RNA sequencing reveals transcriptomic changes in tobacco (Nicotiana tabacum) following NtCPS2 knockdown

Journal

BMC GENOMICS
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12864-021-07796-8

Keywords

CRISPR-Cas9; Nicotiana tabacum; RNASeq; Labdanoid diterpenes; cis-Abienol; Genome editing; Terpenoids

Funding

  1. China National Tobacco Corporation Henan company [[2021]27]
  2. Henan Tobacco Corporation XuChang Company [2020411000240069]
  3. Guizhou Tobacco Corporation Guiyang company [2020-07]
  4. Hunan Tobacco Corporation Changsha Company [21-23A04]
  5. Guangxi Zhuang Autonomous Region Tobacco Corporation Baise Company [2021-4]

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This study utilized CRISPR/Cas9 technology to create transgenic tobacco lines with knockdown of NtCPS2 gene, leading to changes in cis-abienol biosynthesis and related compounds in tobacco. RNA sequencing analysis identified numerous differentially expressed genes, highlighting the involvement of various biological and physiological processes such as diterpenoid biosynthesis and plant hormone signal transduction. Overall, this research provides valuable insights into the regulatory mechanisms of cis-abienol biosynthesis in tobacco.
Background Amber-like compounds form in tobacco (Nicotiana tabacum) during leaf curing and impact aromatic quality. In particular, cis-abienol, a polycyclic labdane-related diterpenoid, is of research interest as a precursor of these compounds. Glandular trichome cells specifically express copalyl diphosphate synthase (NtCPS2) at high levels in tobacco, which, together with NtABS, are major regulators of cis-abienol biosynthesis in tobacco. Results To identify the genes involved in the biosynthesis of cis-abienol in tobacco, we constructed transgenic tobacco lines based on an NtCPS2 gene-knockdown model using CRISPR/Cas9 genome-editing technology to inhibit NtCPS2 function in vitro. In mutant plants, cis-abienol and labdene diol contents decreased, whereas the gibberellin and abscisic acid (ABA) contents increased compared with those in wild-type tobacco plants. RNA sequencing analysis revealed the presence of 9514 differentially expressed genes (DEGs; 4279 upregulated, 5235 downregulated) when the leaves of wild-type and NtCPS2-knockdown tobacco plants were screened. Among these DEGs, the genes encoding cis-abienol synthase, ent-kaurene oxidase, auxin/ABA-related proteins, and transcription factors were found to be involved in various biological and physiochemical processes, including diterpenoid biosynthesis, plant hormone signal transduction, and plant-pathogen interactions. Conclusions The present study provides insight into the unique transcriptome profile of NtCPS2 knockdown tobacco, allowing for a better understanding of the biosynthesis of cis-abienol in tobacco.

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