Affiliation:
1. Department of Biology, Boston College, Chestnut Hill, Massachusetts, USA
Abstract
During muscle development myonuclei undergo a complex set of movements that result in evenly spaced nuclei throughout the muscle cell. In Drosophila two separate pools of Kinesin and Dynein work in synchrony to drive this process. However, how these two pools are specified is not known. Here, we investigate the role of Aplip1 (Drosophila JIP1), a known regulator of both Kinesin and Dynein, in myonuclear positioning. Aplip1 localizes to myotendinous junction and has genetically separable roles in myonuclear positioning and muscle stability. In Aplip1 mutant embryos there was an increase in the percentage of embryos that had both missing and collapsed muscles. Via a separate mechanism, we demonstrate that Aplip1 regulates both the final position of and the dynamic movements of myonuclei. Aplip1 genetically interacts with both Raps and Kinesin to position myonuclei. Furthermore, Dynein and Kinesin localization are disrupted in Aplip1 mutants suggesting that Aplip1-dependent nuclear positioning requires Dynein and Kinesin. Together these data are consistent with Aplip1 having a function within the regulation of Dynein and Kinesin mediated pulling of nuclei from the muscle end.
Funder
American Heart Association
Publisher
The Company of Biologists
Cited by
9 articles.
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