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The laforin/malin E3-ubiquitin ligase complex ubiquitinates pyruvate kinase M1/M2.

ABSTRACT:

Background

Lafora disease (LD, OMIM 254780) is a fatal neurodegenerative disorder produced mainly by mutations in two genes: EPM2A, encoding the dual specificity phosphatase laforin, and EPM2B, encoding the E3-ubiquitin ligase malin. Although it is known that laforin and malin may form a functional complex, the underlying molecular mechanisms of this pathology are still far from being understood.

Methods

In order to gain information about the substrates of the laforin/malin complex, we have carried out a yeast substrate-trapping screening, originally designed to identify substrates of protein tyrosine phosphatases.

Results

Our results identify the two muscular isoforms of pyruvate kinase (PKM1 and PKM2) as novel interaction partners of laforin.

Conclusions

We present evidence indicating that the laforin/malin complex is able to interact with and ubiquitinate both PKM1 and PKM2. This post-translational modification, although it does not affect the catalytic activity of PKM1, it impairs the nuclear localization of PKM2.

SUBMITTER: Viana R

PROVIDER: S-EPMC4619252 | biostudies-literature | 2015 Oct

REPOSITORIES: biostudies-literature

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Publications

The laforin/malin E3-ubiquitin ligase complex ubiquitinates pyruvate kinase M1/M2.

Viana Rosa R Lujan Pablo P Sanz Pascual P

BMC biochemistry 20151023

<h4>Background</h4>Lafora disease (LD, OMIM 254780) is a fatal neurodegenerative disorder produced mainly by mutations in two genes: EPM2A, encoding the dual specificity phosphatase laforin, and EPM2B, encoding the E3-ubiquitin ligase malin. Although it is known that laforin and malin may form a functional complex, the underlying molecular mechanisms of this pathology are still far from being understood.<h4>Methods</h4>In order to gain information about the substrates of the laforin/malin comple ...[more]

PMID: 26493215

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