The AP-2 complex has a specialized clathrin-independent role in apical endocytosis and polar growth in fungi.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28220754.
- Also identified by DOI 10.7554/eLife.20083 and PMC identifier 5338921.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Filamentous fungi provide excellent systems for investigating the role of the AP-2 complex in polar growth. Using <i>Aspergillus nidulans,</i> we show that AP-2 has a clathrin-independent essential role in polarity maintenance and growth. This is in line with a sequence analysis showing that the AP-2 β subunit (β2) of higher fungi lacks a clathrin-binding domain, and experiments showing that AP-2 does not co-localize with clathrin. We provide genetic and cellular evidence that AP-2 interacts with endocytic markers SlaB<sup>End4</sup> and SagA<sup>End3</sup> and the lipid flippases DnfA and DnfB in the sub-apical collar region of hyphae. The role of AP-2 in the maintenance of proper apical membrane lipid and cell wall composition is further supported by its functional interaction with BasA (sphingolipid biosynthesis) and StoA (apical sterol-rich membrane domains), and its essentiality in polar deposition of chitin. Our findings support that the AP-2 complex of dikarya has acquired, in the course of evolution, a specialized clathrin-independent function necessary for fungal polar growth.
Medical subject headings
- Adaptor Protein Complex 2
- Aspergillus nidulans
- Clathrin
- Endocytosis