Regulation of microtubule-based transport by MAP4

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Regulation of microtubule-based transport by MAP4

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Title: Regulation of microtubule-based transport by MAP4
Author: Semenova, Irina; Ikeda, Kazuho; Resaul, Karim; Kraikivski, Pavel; Aguiar, Mike; Gygi, Steven; Zaliapin, Ilya; Cowan, Ann; Rodionov, Vladimir

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Citation: Semenova, Irina, Kazuho Ikeda, Karim Resaul, Pavel Kraikivski, Mike Aguiar, Steven Gygi, Ilya Zaliapin, Ann Cowan, and Vladimir Rodionov. 2014. “Regulation of microtubule-based transport by MAP4.” Molecular Biology of the Cell 25 (20): 3119-3132. doi:10.1091/mbc.E14-01-0022. http://dx.doi.org/10.1091/mbc.E14-01-0022.
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Abstract: Microtubule (MT)-based transport of organelles driven by the opposing MT motors kinesins and dynein is tightly regulated in cells, but the underlying molecular mechanisms remain largely unknown. Here we tested the regulation of MT transport by the ubiquitous protein MAP4 using Xenopus melanophores as an experimental system. In these cells, pigment granules (melanosomes) move along MTs to the cell center (aggregation) or to the periphery (dispersion) by means of cytoplasmic dynein and kinesin-2, respectively. We found that aggregation signals induced phosphorylation of threonine residues in the MT-binding domain of the Xenopus MAP4 (XMAP4), thus decreasing binding of this protein to MTs. Overexpression of XMAP4 inhibited pigment aggregation by shortening dynein-dependent MT runs of melanosomes, whereas removal of XMAP4 from MTs reduced the length of kinesin-2–dependent runs and suppressed pigment dispersion. We hypothesize that binding of XMAP4 to MTs negatively regulates dynein-dependent movement of melanosomes and positively regulates kinesin-2–based movement. Phosphorylation during pigment aggregation reduces binding of XMAP4 to MTs, thus increasing dynein-dependent and decreasing kinesin-2–dependent motility of melanosomes, which stimulates their accumulation in the cell center, whereas dephosphorylation of XMAP4 during dispersion has an opposite effect.
Published Version: doi:10.1091/mbc.E14-01-0022
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196864/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13581248
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