کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2174346 1093792 2009 14 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Molecular dissection of Drosophila Prickle isoforms distinguishes their essential and overlapping roles in planar cell polarity
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Molecular dissection of Drosophila Prickle isoforms distinguishes their essential and overlapping roles in planar cell polarity
چکیده انگلیسی

Prickle-Spiny-Legs (Pk) is an essential component of the planar cell polarity (PCP) pathway, together with Frizzled (Fz) and Dishevelled (Dsh). A role for Pk was proposed to mediate feedback amplification of asymmetric Fz/Dsh activity across cell boundaries, ensuring a single prehair initiates at each distal vertex. Here we show that apical localisation of PkPk and PkSple isoforms are mutually independent and regulated by the C-terminal domain. The N-terminus of PkPk is dispensable for PCP, whereas the unique N-terminal domain of PkSple contains an additional localisation function, which confers a qualitatively different activity. Our results suggest that endogenous PkPk and PkSple can affect each other's function via the C-terminal domain, yet may not form heteromeric complexes. Overexpressing PET domain-deleted Pk variants interferes with a branch of Fz/Dsh signalling that regulates the number of wing hairs, and blocks non-cell-autonomous repolarisation. We infer that PkPk is sufficient to mediate the intercellular feedback signalling. Significantly, PkPk but not PkSple is required for hexagonal cell packing in the pupal wing. We propose that Fz-dependent PCP readout reflects short-range, cell-contact based, interactions between hexagonal cells, rather than a direct response to an as yet unidentified diffusible ligand.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Developmental Biology - Volume 325, Issue 2, 15 January 2009, Pages 386–399
نویسندگان
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