Title |
The laforin/malin E3-ubiquitin ligase complex ubiquitinates pyruvate kinase M1/M2
|
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Published in |
BMC Molecular and Cell Biology, October 2015
|
DOI | 10.1186/s12858-015-0053-6 |
Pubmed ID | |
Authors |
Rosa Viana, Pablo Lujan, Pascual Sanz |
Abstract |
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. 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. Our results identify the two muscular isoforms of pyruvate kinase (PKM1 and PKM2) as novel interaction partners of laforin. 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. |
X Demographics
Geographical breakdown
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United States | 1 | 50% |
Unknown | 1 | 50% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 2 | 100% |
Mendeley readers
Geographical breakdown
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Student > Ph. D. Student | 5 | 21% |
Student > Bachelor | 3 | 13% |
Researcher | 3 | 13% |
Student > Postgraduate | 2 | 8% |
Student > Master | 2 | 8% |
Other | 2 | 8% |
Unknown | 7 | 29% |
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Medicine and Dentistry | 2 | 8% |
Computer Science | 1 | 4% |
Other | 1 | 4% |
Unknown | 8 | 33% |