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First published online 8 April 2008
doi: 10.1242/jcs.020024


Journal of Cell Science 121, 1403-1414 (2008)
Published by The Company of Biologists 2008
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Research Article

Asymmetric localization of the adaptor protein Miranda in neuroblasts is achieved by diffusion and sequential interaction of Myosin II and VI

Veronika Erben1,*, Markus Waldhuber1,2,*, Diana Langer1, Ingrid Fetka1, Ralf Peter Jansen1 and Claudia Petritsch1,2,3,4,{ddagger}

1 GeneCenter, Ludwig-Maximilian-University Munich, Department of Biochemistry and Laboratory of Molecular Biology, 81377 Munich, Germany
2 Department of Neurological Surgery, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA
3 Brain Tumor Research Center, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA
4 Helen Diller Comprehensive Cancer Center, University of California, San Francisco, 513 Parnassus Avenue, San Francisco, CA 94143, USA

{ddagger} Author for correspondence at present address: University of California, San Francisco (UCSF), Department of Neurological Surgery, 513 Parnassus Avenue, San Francisco, CA 94143-0520, USA (e-mail: claudia.petritsch{at}ucsf.edu)

Accepted 5 February 2008

The adaptor protein Miranda plays a pivotal role in the asymmetric cell division of neuroblasts by asymmetrically segregating key differentiation factors. Miranda localization requires Myosin VI and Myosin II. The apical-then-basal localization pattern of Miranda detected in fixed tissue, and the localization defects in embryos lacking Myosin VI, suggest that Miranda is transported to the basal pole as a Myosin VI cargo. However, the mode and temporal sequence of Miranda localization have not been characterized in live embryos. Furthermore, it is unknown whether Miranda and PON, a second adaptor protein required for asymmetric protein localization, are both regulated by Myosin II. By combining immunofluorescence studies with time-lapse confocal microscopy, we show that Miranda protein forms an apical crescent at interphase, but is ubiquitously localized at prophase in a Myosin-II-dependent manner. FRAP analysis revealed that Miranda protein reaches the basal cortex by passive diffusion throughout the cell, rather than by long-range Myosin VI-directed transport. Myosin VI acts downstream of Myosin II in the same pathway to deliver diffusing Miranda to the basal cortex. PON localization occurs mainly along the cortex and requires Myosin II but not Myosin VI, suggesting that distinct mechanisms are employed to localize different adaptor proteins during asymmetric cell division.

Key words: Mechanism for asymmetric cell division, Stem cells, Miranda, PON, Myosin II and VI


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R. Sousa-Nunes, W. Chia, and W. G. Somers
Protein Phosphatase 4 mediates localization of the Miranda complex during Drosophila neuroblast asymmetric divisions
Genes & Dev., February 1, 2009; 23(3): 359 - 372.
[Abstract] [Full Text] [PDF]


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DevelopmentHome page
V. Erben, M. Waldhuber, D. Langer, I. Fetka, R. P. Jansen, and C. Petritsch
Asymmetric localization of the adaptor protein Miranda in neuroblasts is achieved by diffusion and sequential interaction of Myosin II and VI
Development, May 15, 2008; 135(10): e1 - e1.
[Full Text]




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