Functional Conservation and Divergence of daf-22 Paralogs in Pristionchus pacificus Dauer Development. (28th April 2016)

• Record Type: Journal Article
• Authors: Markov, Gabriel V.; Meyer, Jan M.; Panda, Oishika; Artyukhin, Alexander B.; Claaßen, Marc; Witte, Hanh; Schroeder, Frank C.; Sommer, Ralf J.
• Is Part Of: Molecular biology and evolution. Volume 33:Number 10(2016:Oct.)
• Page Start: 2506
• Page End: 2514
• Publication Date: 2016-04-28
• Subjects: dauer development -- phenotypic plasticity -- C. elegans -- Pristionchus pacificus -- daf-22 -- ascarosides -- β-oxidation.; Molecular biology -- Periodicals; Molecular evolution -- Periodicals; Evolution, Molecular -- Periodicals; Molecular Biology -- Periodicals; 572.8
• DOI: 10.1093/molbev/msw090
• Languages: English
• ISSNs: 0737-4038

Abstract

Abstract: Small-molecule signaling in nematode dauer formation has emerged as a major model to study chemical communication in development and evolution. Developmental arrest as nonfeeding and stress-resistant dauer larvae represents the major survival and dispersal strategy. Detailed studies in Caenorhabditis elegans and Pristionchus pacificus revealed that small-molecule communication changes rapidly in evolution resulting in extreme structural diversity of small-molecule compounds. In C. elegans, a blend of ascarosides constitutes the dauer pheromone, whereas the P. pacificus dauer pheromone includes additional paratosides and integrates building blocks from diverse primary metabolic pathways. Despite this complexity of small-molecule structures and functions, little is known about the biosynthesis of small molecules in nematodes outside C. elegans . Here, we show that the genes encoding enzymes of the peroxisomal β-oxidation pathway involved in small-molecule biosynthesis evolve rapidly, including gene duplications and domain switching. The thiolase daf-22, the most downstream factor in C. elegans peroxisomal β-oxidation, has duplicated in P. pacificus, resulting in Ppa-daf-22.1, which still contains the sterol-carrier-protein (SCP) domain that was lost in C. elegans daf-22, and Ppa-daf-22.2. Using the CRISPR/Cas9 system, we induced mutations in both P. pacificus daf-22 genes and identified an unexpected complexity of functional conservation and divergence. Under well-fed conditions, ascaroside biosynthesis proceeds exclusively via Ppa-daf-22.1 . In contrast, starvation conditions induce Ppa-daf-22.2 activity, resulting in the production of a specific subset of ascarosides. Gene expression studies indicate a reciprocal up-regulation of both Ppa-daf-22 genes, which is, however, independent of starvation. Thus, our study reveals an unexpected functional complexity of dauer development and evolution.