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The activity of hyaluronan synthase 2 is regulated by dimerization and ubiquitination.

ABSTRACT: Hyaluronan is a component of the extracellular matrix, which affects tissue homeostasis. In this study, we investigated the regulatory mechanisms of one of the hyaluronan-synthesizing enzymes, HAS2. Ectopic expression of Flag- and 6myc-HAS2 in COS-1 cells followed by immunoprecipitation and immunoblotting revealed homodimers; after co-transfection with Flag-HAS3, also heterodimers were seen. Furthermore, the expressed HAS2 was ubiquitinated. We identified one acceptor site for ubiquitin on lysine residue 190. Mutation of this residue led to inactivation of the enzymatic activity of HAS2. Interestingly, K190R-mutated HAS2 formed dimers with wt HAS2 and quenched the activity of wt HAS2, thus demonstrating a functional role of the dimeric configuration.

SUBMITTER: Karousou E

PROVIDER: S-EPMC2911313 | biostudies-literature | 2010 Jul

REPOSITORIES: biostudies-literature

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The activity of hyaluronan synthase 2 is regulated by dimerization and ubiquitination.

Karousou Eugenia E Kamiryo Masaru M Skandalis Spyros S SS Ruusala Aino A Asteriou Trias T Passi Alberto A Yamashita Hidetoshi H Hellman Ulf U Heldin Carl-Henrik CH Heldin Paraskevi P

The Journal of biological chemistry 20100527 31

Hyaluronan is a component of the extracellular matrix, which affects tissue homeostasis. In this study, we investigated the regulatory mechanisms of one of the hyaluronan-synthesizing enzymes, HAS2. Ectopic expression of Flag- and 6myc-HAS2 in COS-1 cells followed by immunoprecipitation and immunoblotting revealed homodimers; after co-transfection with Flag-HAS3, also heterodimers were seen. Furthermore, the expressed HAS2 was ubiquitinated. We identified one acceptor site for ubiquitin on lysin ...[more]

PMID: 20507985

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| S-EPMC5383204 | biostudies-literature

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