Genetic Modifier Screens Reveal New Components that Interact with the Drosophila Dystroglycan-Dystrophin Complex

被引:49
作者
Kucherenko, Mariya M. [1 ,2 ]
Pantoja, Mario [1 ]
Yatsenko, Andriy S. [1 ,2 ]
Shcherbata, Halyna R. [1 ]
Fischer, Karin A. [1 ]
Maksymiv, Dariya V. [1 ,2 ]
Chernyk, Yaroslava I. [1 ,2 ]
Ruohola-Baker, Hannele [1 ]
机构
[1] Univ Washington, Dept Biochem, Inst Stem Cell & Regenerat Med, Seattle, WA 98195 USA
[2] Ivan Franko Natl Univ Lviv, Dept Genet & Biotechnol, Lvov, Ukraine
来源
PLOS ONE | 2008年 / 3卷 / 06期
关键词
D O I
10.1371/journal.pone.0002418
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Dystroglycan-Dystrophin (Dg-Dys) complex has a capacity to transmit information from the extracellular matrix to the cytoskeleton inside the cell. It is proposed that this interaction is under tight regulation; however the signaling/regulatory components of Dg-Dys complex remain elusive. Understanding the regulation of the complex is critical since defects in this complex cause muscular dystrophy in humans. To reveal new regulators of the Dg-Dys complex, we used a model organism Drosophila melanogaster and performed genetic interaction screens to identify modifiers of Dg and Dys mutants in Drosophila wing veins. These mutant screens revealed that the Dg-Dys complex interacts with genes involved in muscle function and components of Notch, TGF-beta and EGFR signaling pathways. In addition, components of pathways that are required for cellular and/or axonal migration through cytoskeletal regulation, such as Semaphorin-Plexin, Frazzled-Netrin and Slit-Robo pathways show interactions with Dys and/or Dg. These data suggest that the Dg-Dys complex and the other pathways regulating extracellular information transfer to the cytoskeletal dynamics are more intercalated than previously thought.
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页数:14
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