Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry

LT Jae, M Raaben, M Riemersma, E Van Beusekom… - Science, 2013 - science.org
LT Jae, M Raaben, M Riemersma, E Van Beusekom, VA Blomen, A Velds, RM Kerkhoven…
Science, 2013science.org
Glycosylated α-dystroglycan (α-DG) serves as cellular entry receptor for multiple pathogens,
and defects in its glycosylation cause hereditary Walker-Warburg syndrome (WWS). At least
eight proteins are critical to glycosylate α-DG, but many genes mutated in WWS remain
unknown. To identify modifiers of α-DG, we performed a haploid screen for Lassa virus entry,
a hemorrhagic fever virus causing thousands of deaths annually that hijacks glycosylated α-
DG to enter cells. In complementary screens, we profiled cells for absence of α-DG …
Glycosylated α-dystroglycan (α-DG) serves as cellular entry receptor for multiple pathogens, and defects in its glycosylation cause hereditary Walker-Warburg syndrome (WWS). At least eight proteins are critical to glycosylate α-DG, but many genes mutated in WWS remain unknown. To identify modifiers of α-DG, we performed a haploid screen for Lassa virus entry, a hemorrhagic fever virus causing thousands of deaths annually that hijacks glycosylated α-DG to enter cells. In complementary screens, we profiled cells for absence of α-DG carbohydrate chains or biochemically related glycans. This revealed virus host factors and a suite of glycosylation units, including all known Walker-Warburg genes and five additional factors critical for the modification of α-DG. Our findings accentuate the complexity of this posttranslational feature and point out genes defective in dystroglycanopathies.
AAAS
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