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Label-Free Non-Linear Optics for the Study of Tubulin-Dependent Defects in Central Myelin
Published on: March 24, 2023
The microtubule-associated protein tumor overexpressed gene/cytoskeleton-associated protein 5 is necessary for myelin
Victor P Francone1, Michael J Maggipinto, Linda D Kosturko
1Department of Neuroscience, University of Connecticut Health Center, Farmington, Connecticut 06030, USA.
Abstract:
Tumor overexpressed gene (TOG) protein, encoded by cytoskeleton-associated protein CKAP5, is a microtubule-associated protein that binds to heterogeneous nuclear ribonucleoprotein (hnRNP) A2. hnRNP A2 is an RNA trafficking factor that associates with myelin basic protein (MBP) mRNA. In oligodendrocytes, TOG, hnRNP A2, and MBP mRNA colocalize in granules that assemble in the perikaryon and are transported to the peripheral network of processes that extends from it. MBP accumulates preferentially in the membrane of the medial and distal portions of these cellular processes. MBP expression was reduced when TOG level was lowered by short-hairpin (sh) RNA. The reduction in TOG did not affect overall cell morphology or the assembly, transport, localization, or number of MBP mRNA-containing granules. Reduced levels of TOG did not affect another oligodendrocyte-specific component, myelin oligodendrocyte glycoprotein, which is expressed at the same time as MBP but translated from mRNA localized in the cell body. Expression in a neural cell line of a green fluorescent protein (GFP)-MBP fusion protein derived from a construct containing GFP and the full-length cDNA for the rat 14 kDa MBP was reduced when TOG level was lowered by shRNA treatment. Expression of GFP, derived from GFP mRNA containing the hnRNP A2 binding element of MBP mRNA, was similarly reduced in cells with low TOG levels. These data indicate that TOG is necessary for efficient translation of MBP mRNA and suggest that this role is mediated by its interaction with hnRNP A2.
Insights
Tumor overexpressed gene (TOG) protein is crucial for myelin basic protein (MBP) mRNA translation in oligodendrocytes. TOG interacts with hnRNP A2 to facilitate MBP expression, impacting myelin sheath formation.
Area of Science:
- Neuroscience
- Molecular Biology
- Cell Biology
Background:
- Tumor overexpressed gene (TOG) protein, encoded by CKAP5, is a microtubule-associated protein.
- TOG interacts with heterogeneous nuclear ribonucleoprotein (hnRNP) A2, an RNA trafficking factor.
- hnRNP A2 associates with myelin basic protein (MBP) mRNA in oligodendrocytes.
Purpose of the Study:
- To investigate the role of TOG in MBP mRNA expression and oligodendrocyte function.
- To elucidate the mechanism by which TOG influences MBP translation.
Main Methods:
- Utilized short-hairpin (sh) RNA to reduce TOG levels in neural cell lines and oligodendrocytes.
- Examined the localization and transport of MBP mRNA-containing granules.
- Assessed MBP and myelin oligodendrocyte glycoprotein expression.
- Expressed GFP-MBP fusion proteins and GFP with MBP mRNA elements.
Main Results:
- Reduced TOG levels decreased MBP expression without affecting cell morphology or granule dynamics.
- TOG reduction did not impact myelin oligodendrocyte glycoprotein expression.
- Expression of GFP-MBP fusion protein and GFP containing MBP mRNA elements was reduced with lower TOG levels.
Conclusions:
- TOG is essential for efficient translation of MBP mRNA.
- TOG's role in MBP translation is likely mediated through its interaction with hnRNP A2.
- This interaction is critical for oligodendrocyte function and myelin formation.
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