Divergent mitochondrial and endoplasmic reticulum association of DMPK splice isoforms depends on unique sequence arrangements in tail anchors
Molecular and Cellular Biology, ISSN: 0270-7306, Vol: 25, Issue: 4, Page: 1402-1414
2005
- 23Citations
- 31Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations23
- Citation Indexes23
- 23
- CrossRef19
- Captures31
- Readers31
- 31
Article Description
Myotonic dystrophy protein kinase (DMPK) is a Ser/Thr-type protein kinase with unknown function, originally identified as the product of the gene that is mutated by triplet repeat expansion in patients with myotonic dystrophy type 1 (DM1). Alternative splicing of DMPK transcripts results in multiple protein isoforms carrying distinct C termini. Here, we demonstrate by expressing individual DMPKs in various cell types, including CC and DMPK myoblast cells, that unique sequence arrangements in these tails control the specificity of anchoring into intracellular membranes. Mouse DMPK A and C were found to associate specifically with either the endoplasmic reticulum (ER) or the mitochondrial outer membrane, whereas the corresponding human DMPK A and C proteins both localized to mitochondria. Expression of mouse and human DMPK A-but not C-isoforms in mammalian cells caused clustering of ER or mitochondria. Membrane association of DMPK isoforms was resistant to alkaline conditions, and mutagenesis analysis showed that proper anchoring was differentially dependent on basic residues flanking putative transmembrane domains, demonstrating that DMPK tails form unique tail anchors. This work identifies DMPK as the first kinase in the class of tail-anchored proteins, with a possible role in organelle distribution and dynamics.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=13444252580&origin=inward; http://dx.doi.org/10.1128/mcb.25.4.1402-1414.2005; http://www.ncbi.nlm.nih.gov/pubmed/15684391; http://mcb.asm.org/cgi/doi/10.1128/MCB.25.4.1402-1414.2005; https://syndication.highwire.org/content/doi/10.1128/MCB.25.4.1402-1414.2005; https://www.tandfonline.com/doi/full/10.1128/MCB.25.4.1402-1414.2005; https://dx.doi.org/10.1128/mcb.25.4.1402-1414.2005; https://mcb.asm.org/content/25/4/1402; https://mcb.asm.org/content/25/4/1402.abstract; https://mcb.asm.org/content/25/4/1402.full.pdf; https://journals.asm.org/doi/10.1128/MCB.25.4.1402-1414.2005; https://journals.asm.org/doi/abs/10.1128/MCB.25.4.1402-1414.2005; http://mcb.asm.org/content/25/4/1402; https://mcb.asm.org/content/mcb/25/4/1402.full.pdf
American Society for Microbiology
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