Literature DB >> 24726363

Fly-FUCCI: A versatile tool for studying cell proliferation in complex tissues.

Norman Zielke1, Jerome Korzelius1, Monique van Straaten1, Katharina Bender1, Gregor F P Schuhknecht1, Devanjali Dutta1, Jinyi Xiang1, Bruce A Edgar2.   

Abstract

One promising approach for in vivo studies of cell proliferation is the FUCCI system (fluorescent ubiquitination-based cell cycle indicator). Here, we report the development of a Drosophila-specific FUCCI system (Fly-FUCCI) that allows one to distinguish G1, S, and G2 phases of interphase. Fly-FUCCI relies on fluorochrome-tagged degrons from the Cyclin B and E2F1 proteins, which are degraded by the ubiquitin E3-ligases APC/C and CRL4(Cdt2), during mitosis or the onset of S phase, respectively. These probes can track cell-cycle patterns in cultured Drosophila cells, eye and wing imaginal discs, salivary glands, the adult midgut, and probably other tissues. To support a broad range of experimental applications, we have generated a toolkit of transgenic Drosophila lines that express the Fly-FUCCI probes under control of the UASt, UASp, QUAS, and ubiquitin promoters. The Fly-FUCCI system should be a valuable tool for visualizing cell-cycle activity during development, tissue homeostasis, and neoplastic growth.
Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 24726363     DOI: 10.1016/j.celrep.2014.03.020

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  94 in total

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