期刊
BMC BIOLOGY
卷 19, 期 1, 页码 -出版社
BMC
DOI: 10.1186/s12915-021-01001-8
关键词
Fatty acyl desaturase; Gene family evolution; Bifunctional; Conjugated double bond; Tortricidae
类别
资金
- European Union's Horizon 2020 research and innovation programme [760798]
- Swedish Foundation for Strategic Research (Oil Crops for the Future) [RBP 14-0037]
- Swedish Research Council
- Formas
- Royal Physiographic Society in Lund
- Lund University
This study identified the role of the FAD gene family in the biosynthesis of sex pheromones in the codling moth, revealing wide distribution and diverse expression patterns of FAD genes in the genome. The gene Cpo_CPRQ, exclusively expressed in the female pheromone gland, was found to encode an FAD with unique desaturation activities. The evolution of the signature pheromone structure in olethreutine moths was shown to depend on an ancient gene expansion.
Background Defining the origin of genetic novelty is central to our understanding of the evolution of novel traits. Diversification among fatty acid desaturase (FAD) genes has played a fundamental role in the introduction of structural variation in fatty acyl derivatives. Because of its central role in generating diversity in insect semiochemicals, the FAD gene family has become a model to study how gene family expansions can contribute to the evolution of lineage-specific innovations. Here we used the codling moth (Cydia pomonella) as a study system to decipher the proximate mechanism underlying the production of the increment 8 increment 10 signature structure of olethreutine moths. Biosynthesis of the codling moth sex pheromone, (E8,E10)-dodecadienol (codlemone), involves two consecutive desaturation steps, the first of which is unusual in that it generates an E9 unsaturation. The second step is also atypical: it generates a conjugated diene system from the E9 monoene C-12 intermediate via 1,4-desaturation. Results Here we describe the characterization of the FAD gene acting in codlemone biosynthesis. We identify 27 FAD genes corresponding to the various functional classes identified in insects and Lepidoptera. These genes are distributed across the C. pomonella genome in tandem arrays or isolated genes, indicating that the FAD repertoire consists of both ancient and recent duplications and expansions. Using transcriptomics, we show large divergence in expression domains: some genes appear ubiquitously expressed across tissue and developmental stages; others appear more restricted in their expression pattern. Functional assays using heterologous expression systems reveal that one gene, Cpo_CPRQ, which is prominently and exclusively expressed in the female pheromone gland, encodes an FAD that possesses both E9 and increment 8 increment 10 desaturation activities. Phylogenetically, Cpo_CPRQ clusters within the Lepidoptera-specific increment 10/ increment 11 clade of FADs, a classic reservoir of unusual desaturase activities in moths. Conclusions Our integrative approach shows that the evolution of the signature pheromone structure of olethreutine moths relied on a gene belonging to an ancient gene expansion. Members of other expanded FAD subfamilies do not appear to play a role in chemical communication. This advises for caution when postulating the consequences of lineage-specific expansions based on genomics alone.
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