Homology and Modular Evolution of CATCHR at the Origin of the Eukaryotic Endomembrane System. (1st June 2021)

• Record Type: Journal Article
• Authors: Santana-Molina, Carlos; Gutierrez, Fernando; Devos, Damien P
• Editors: Golding, Brian
• Is Part Of: Genome biology and evolution. Volume 13:Number 7(2021)
• Publication Date: 2021-06-01
• Subjects: CATCHR -- exocyst -- COG -- GARP -- DSL1 -- membrane trafficking -- protein-complex evolution -- paralogs; Genomics -- Periodicals; Genes -- Periodicals; 572.8605
• DOI: 10.1093/gbe/evab125
• Languages: English
• ISSNs: 1759-6653

Abstract

Abstract: The membrane trafficking is an essential process of eukaryotic cells, as it manages vesicular trafficking toward different parts of the cell. In this process, membrane fusions between vesicles and target membranes are mediated by several factors, including the multisubunit tethering complexes. One type of multisubunit tethering complex, the complexes associated with tethering containing helical rods (CATCHR), encompasses the exocyst, COG, GARP, and DSL1 complexes. The CATCHR share similarities at sequence, structural, and protein-complex organization level although their actual relationship is still poorly understood. In this study, we have re-evaluated CATCHR at different levels, demonstrating that gene duplications followed by neofunctionalization, were key for their origin. Our results, reveals that there are specific homology relationships and parallelism within and between the CATCHR suggesting that most of these complexes are composed by modular tetramers of four different kinds of proteins, three of them having a clear common origin. The extension of CATCHR family occurred concomitantly with the protein family expansions of their molecular partners, such as small GTPases and SNAREs, among others, and likely providing functional specificity. Our results provide novel insights into the structural organization and mechanism of action of CATCHR, with implications for the evolution of the endomembrane system of eukaryotes and promoting CATCHR as ideal candidates to study the evolution of multiprotein complexes.