Predicted glycosyltransferases promote development and prevent spurious cell clumping in the choanoflagellate <i>S. rosetta</i>.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30556809.
- Also identified by DOI 10.7554/eLife.41482 and PMC identifier 6322860.
- 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
In a previous study we established forward genetics in the choanoflagellate <i>Salpingoeca rosetta</i> and found that a C-type lectin gene is required for rosette development (Levin <i>et al.</i>, 2014). Here we report on critical improvements to genetic screens in <i>S. rosetta</i> while also investigating the genetic basis for rosette defect mutants in which single cells fail to develop into orderly rosettes and instead aggregate promiscuously into amorphous clumps of cells. Two of the mutants, Jumble and Couscous, mapped to lesions in genes encoding two different predicted glycosyltransferases and displayed aberrant glycosylation patterns in the basal extracellular matrix (ECM). In animals, glycosyltransferases sculpt the polysaccharide-rich ECM, regulate integrin and cadherin activity, and, when disrupted, contribute to tumorigenesis. The finding that predicted glycosyltransferases promote proper rosette development and prevent cell aggregation in <i>S. rosetta</i> suggests a pre-metazoan role for glycosyltransferases in regulating development and preventing abnormal tumor-like multicellularity.
Medical subject headings
- Choanoflagellata
- Glycosyltransferases
- Mutation
- Protozoan Proteins