Cas1p is a membrane protein necessary for the O‐acetylation of the Cryptococcus neoformans capsular polysaccharide

G Janbon, U Himmelreich, F Moyrand… - Molecular …, 2001 - Wiley Online Library
G Janbon, U Himmelreich, F Moyrand, L Improvisi, F Dromer
Molecular microbiology, 2001Wiley Online Library
The capsule is certainly the most obvious virulence factor for Cryptococcus neoformans. The
main capsule constituents are glucuronoxylomannans (GXM). Several studies have focused
on the structure and chemistry of the GXM component of the capsule, yet little is known
about the genetic basis of the capsule construction. Using a monoclonal antibody specific to
a sugar epitope, we isolated a capsule‐structure mutant strain and cloned by
complementation a gene named CAS1 that codes for a putative membrane protein …
The capsule is certainly the most obvious virulence factor for Cryptococcus neoformans. The main capsule constituents are glucuronoxylomannans (GXM). Several studies have focused on the structure and chemistry of the GXM component of the capsule, yet little is known about the genetic basis of the capsule construction. Using a monoclonal antibody specific to a sugar epitope, we isolated a capsule‐structure mutant strain and cloned by complementation a gene named CAS1 that codes for a putative membrane protein. Although no sequence homology was found with any known protein in the different databases, protein analysis using the Propsearch software classified Cas1p as a putative glycosyltransferase. Cas1p is a well‐conserved evolutionary protein, as we identified one orthologue in the human genome, one in the drosophila genome and four in the plant Arabidopsis thaliana genome. Analysis of the capsule structure after CAS1 deletion showed that it is required for GXM O‐acetylation.
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