Numerous examples of biosynthetic gene clusters (BGCs) have been discovered in plant genomes, but little is known about the formation of these important examples of gene organization.
They are of interest because many of BGCs reported in plants in recent years encode compounds of agricultural importance, conferring disease resistance and drought tolerance.
Investigating this genome architecture is crucial to our understanding of the relationship between genome organization and the evolution of complex adaptive traits.
John Innes Centre researchers in the Osbourn group took advantage of recent advances in sequence data for Arabidopsis thaliana and its relatives in a study which sheds light on the occurrence, nature and evolution of plant BGCs.
The large scale analysis, focussing on the thalianol BCG, identifies new genetic drivers underlying non-random gene organization. It highlights the importance of chromosomal inversions, as a molecular mechanism that may shuffle more distant genes into the cluster so enabling cluster compaction.
Although the role of chromosomal inversions in evolution in animals has been extensively investigated, examples of these large-scale mutations in plants are rare.
This is the first evidence to suggest that chromosomal inversion may lead to cluster compaction. The study suggests that by suppressing genetic recombination chromosomal inversion may insulate clustered co-adapted genes against dispersal.
First author Zhenhua Liu from the John Innes Centre explains: “Our study is exciting because we uncovered genetic drivers, particularly chromosomal inversions, which likely play significant roles in maintenance and diversification of plant BGCs.
“Our findings not only provide fundamental understanding of how plant BGCs evolve, but also advance prediction and identification of BGCs in complex plant genomes.”
Next the researchers in the Osbourn group will extend analysis towards other types of plant BGCs in order to investigate evolutionary dynamics, patterns and forces that shape plant BGCs.
Source: John Innes Centre
