Identification of regions required for allelic specificity at the cell wall remodeling allorecognition checkpoint in Neurospora crassa.

Abstract

Allorecognition is the ability of organisms/cells to differentiate self from nonself. In Neurospora crassa, allorecognition systems serve as checkpoints to restrict germling/hyphal fusion between genetically incompatible strains. The cell wall remodeling (cwr) checkpoint functions after chemotrophic interactions and is triggered upon cell/hyphal contact, regulating cell wall dissolution and subsequent cell fusion. The cwr region consists of 2 linked loci, cwr-1 and cwr-2, that are under severe linkage disequilibrium. Phylogenetic analyses of N. crassa populations showed that cwr-1/cwr-2 alleles fall into 6 different haplogroups. Strains containing deletions of cwr-1 and cwr-2 fuse with previously haplogroup incompatible cells, indicating that cwr negatively regulates cell fusion. CWR-1 encodes a chitin polysaccharide monooxygenase; the polysaccharide monooxygenase (PMO) domain confers allelic specificity by interacting in trans with the predicted transmembrane protein, CWR-2, from a different haplogroup. However, catalytic activity of CWR-1 is not required for triggering a block in cell fusion. Two variable regions of CWR-1 (L2 and LC) in the PMO domain show high levels of structural variability between different haplogroups. CWR-1 chimeras containing a LC region from a different haplogroup were sufficient to trigger a cell fusion block, suggesting that the complete PMO domain structure is necessary for allorecognition. Modeling of the transmembrane protein CWR-2 revealed allelic variability in the 2 major extracellular domains (ED2/ED4). Chimeras of CWR-2 with swapped ED2 or ED4 or ED2/ED4 from different cwr-2 haplogroups also altered allelic specificity. This work identified key regions of CWR-1 and CWR-2 that contribute to allorecognition specificity, providing insight into the molecular basis of this process.