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ACTIN-DIRECTED TOXIN. ACD toxin-produced actin oligomers poison formin-controlled actin polymerization.


ABSTRACT: The actin cross-linking domain (ACD) is an actin-specific toxin produced by several pathogens, including life-threatening spp. of Vibrio cholerae, Vibrio vulnificus, and Aeromonas hydrophila. Actin cross-linking by ACD is thought to lead to slow cytoskeleton failure owing to a gradual sequestration of actin in the form of nonfunctional oligomers. Here, we found that ACD converted cytoplasmic actin into highly toxic oligomers that potently "poisoned" the ability of major actin assembly proteins, formins, to sustain actin polymerization. Thus, ACD can target the most abundant cellular protein by using actin oligomers as secondary toxins to efficiently subvert cellular functions of actin while functioning at very low doses.

SUBMITTER: Heisler DB 

PROVIDER: S-EPMC4648357 | biostudies-literature | 2015 Jul

REPOSITORIES: biostudies-literature

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ACTIN-DIRECTED TOXIN. ACD toxin-produced actin oligomers poison formin-controlled actin polymerization.

Heisler David B DB   Kudryashova Elena E   Grinevich Dmitry O DO   Suarez Cristian C   Winkelman Jonathan D JD   Birukov Konstantin G KG   Kotha Sainath R SR   Parinandi Narasimham L NL   Vavylonis Dimitrios D   Kovar David R DR   Kudryashov Dmitri S DS  

Science (New York, N.Y.) 20150701 6247


The actin cross-linking domain (ACD) is an actin-specific toxin produced by several pathogens, including life-threatening spp. of Vibrio cholerae, Vibrio vulnificus, and Aeromonas hydrophila. Actin cross-linking by ACD is thought to lead to slow cytoskeleton failure owing to a gradual sequestration of actin in the form of nonfunctional oligomers. Here, we found that ACD converted cytoplasmic actin into highly toxic oligomers that potently "poisoned" the ability of major actin assembly proteins,  ...[more]

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