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MAP6 interacts with Tctex1 and Cav 2.2/N-type calcium channels to regulate calcium signalling in neurons.


ABSTRACT: MAP6 proteins were first described as microtubule-stabilizing agents, whose properties were thought to be essential for neuronal development and maintenance of complex neuronal networks. However, deletion of all MAP6 isoforms in MAP6 KO mice does not lead to dramatic morphological aberrations of the brain but rather to alterations in multiple neurotransmissions and severe behavioural impairments. A search for protein partners of MAP6 proteins identified Tctex1 - a dynein light chain with multiple non-microtubule-related functions. The involvement of Tctex1 in calcium signalling led to investigate it in MAP6 KO neurons. In this study, we show that functional Cav 2.2/N-type calcium channels are deficient in MAP6 KO neurons, due to improper location. We also show that MAP6 proteins interact directly with both Tctex1 and the C-terminus of Cav 2.2/N-type calcium channels. A balance of these two interactions seems to be crucial for MAP6 to modulate calcium signalling in neurons.

SUBMITTER: Brocard J 

PROVIDER: S-EPMC5765474 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature

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MAP6 interacts with Tctex1 and Ca<sub>v</sub> 2.2/N-type calcium channels to regulate calcium signalling in neurons.

Brocard Jacques J   Dufour Fabrice F   Gory-Fauré Sylvie S   Arnoult Christophe C   Bosc Christophe C   Denarier Eric E   Peris Leticia L   Saoudi Yasmina Y   De Waard Michel M   Andrieux Annie A  

The European journal of neuroscience 20171122 11


MAP6 proteins were first described as microtubule-stabilizing agents, whose properties were thought to be essential for neuronal development and maintenance of complex neuronal networks. However, deletion of all MAP6 isoforms in MAP6 KO mice does not lead to dramatic morphological aberrations of the brain but rather to alterations in multiple neurotransmissions and severe behavioural impairments. A search for protein partners of MAP6 proteins identified Tctex1 - a dynein light chain with multipl  ...[more]

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