Characterisation of phospholipid: diacylglycerol acyltransferases (PDATs) from and their roles in stress responses.

As an important oilseed worldwide, is being increasingly explored for its use in production of food, feed, biofuel and industrial chemicals. However, detailed mechanisms of camelina oil biosynthesis and accumulation, particularly in vegetative tissues, are understood to a very small extent. Here, we present genome-wide identification, cloning and functional analysis of phospholipid diacylglycerol acyltransferase (PDAT) in , which catalyses the final acylation step in triacylglycerol (TAG) biosynthesis by transferring a fatty acyl moiety from a phospholipid to diacylglycerol (DAG). We identified five genes (namely , , and and and ) encoding PDATs from the camelina genome. is mainly expressed in seeds, whereas preferentially accumulates in flower and leaf tissues. High expression of and was detected in stem and root tissues, respectively. Cold stress induced upregulation of and expression by 3.5- and 2.5-fold, respectively, compared to the control. Salt stress led to an increase in transcripts by 5.1-fold. Drought treatment resulted in an enhancement of mRNAs by twofold and a reduction of expression. Osmotic stress upregulated the expression of by 3.3-fold. Furthermore, the cDNA clones of these genes were isolated for transient expression in tobacco leaves. All five genes showed PDAT enzymatic activity and substantially increased TAG accumulation in the leaves, with CsPDAT1-A showing a higher preference for ɑ-linolenic acid (18:3 ω-3). Overall, this study demonstrated that different members of CsPDAT family contribute to TAG synthesis in different tissues. More importantly, they are involved in different types of stress responses in camelina seedlings, providing new evidence of their roles in oil biosynthesis and regulation in camelina vegetative tissue. The identified CsPDATs may have practical applications in increasing oil accumulation and enhancing stress tolerance in other plants as well.