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doi: 10.1242/10.1242/jcs.00297
Research Article |
1 Institute of Molecular and Cell Biology, 30 Medical Drive, Singapore
117609
2 MRC Centre for Developmental Neurobiology, King's College London, New Hunts
House, Guy's Campus, London SE1 1UL, UK
* Authors for correspondence (e-mail: william.chia{at}kcl.ac.uk; mcbyangn{at}imcb.nus.edu.sg)
Accepted 28 November 2002
Asymmetric cell division is a fundamental mechanism used to generate
cellular diversity in invertebrates and vertebrates. In Drosophila,
asymmetric division of neuroblasts is achieved by the asymmetric segregation
of cell fate determinants Prospero and Numb into the basal daughter cell.
Asymmetric segregation of cell fate determinants requires an apically
localized protein complex that includes Inscuteable, Pins, Bazooka, DmPar-6,
DaPKC and G
i. Pins acts to stabilize the apical complex during
neuroblast divisions. Pins interacts and colocalizes with Inscuteable, as well
as maintaining its apical localization. We have isolated a mouse homologue of
pins (Pins) and characterized its expression profile. Mouse
PINS shares high similarity in sequence and structure with Pins and other
Pins-like proteins from mammals. Pins is expressed in many mouse
tissues but its expression is enriched in the ventricular zone of the
developing central nervous systems. PINS localizes asymmetrically to the
apical cortex of mitotic neuroblasts when ectopically expressed in
Drosophila embryos. Like Pins, its N-terminal tetratricopeptide
repeats can directly interact with the asymmetric localization domain of Insc,
and its C-terminal GoLoco-containing region can direct localization to the
neuroblast cortex. We further show that Pins can fulfill all aspects
of pins function in Drosophila neuroblast asymmetric cell
divisions. Our results suggest a conservation of function between the fly and
mammalian Pins homologues.
Key words: Mouse Pins, pins, Asymmetric cell division, Neuroblasts, Drosophila
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