Abstract

We developed a new variant of coral-derived red fluorescent protein, DsRed S197Y, which is brighter and essentially free from secondary fluorescence peak. This makes it an ideal reporter for double labeling with green fluorescent protein (GFP). Though purified protein shows only 20% stronger fluorescence emission, culture cells that express DsRed S197Y exhibit a 3-3.5 times higher level of fluorescence than the cells that express wild-type DsRed. The much slower fluorescence maturation of DsRed than that of GFP is a beneficial feature for a fluorescent developmental timer application. When GFP and DsRed S197Y are expressed simultaneously, emissions start at different latency. This provides information about the time after the onset of expression. It reflects the order of cell differentiation if the expression is activated upon differentiation of certain types of cells. We applied this system to the developing brain of Drosophila and visualized, for the first time, the formation order of neural fibers within a large bundle. Our results showed that newly extending fibers of the mushroom body neurons mainly run into the core rather than to the periphery of the existing bundle. DsRed-based timer thus presents an indispensable tool for developmental biology and genetics of model organisms.

Highlights

  • From the ‡Tsukita Cell Axis Project, Exploratory Research for Advanced Technology (ERATO), Japan Science and Technology Corporation (JST), Kyoto Research Park, Kyoto 600-8813, ¶National Institute for Basic Biology, Okazaki 444-8585, ʈDivision of Biological Science, Nagoya University, Nagoya 464-8602, ‡‡Department of Cell Biology, Faculty of Medicine, Kyoto University, Kyoto 606-8501, and **Precursory Research for Embryonic Science and Technology (PRESTO), JST, Okazaki 444-8585, Japan

  • We developed a new variant of coral-derived red fluorescent protein, DsRed Ser-197 to Tyr (S197Y), which is brighter and essentially free from secondary fluorescence peak

  • Cell Culture and Lysate Preparation—For time course analysis, E. coli carrying EGFP, wild-type DsRed, or DsRed S197Y in the pET-11 plasmids were grown until OD ϭ 1.0 in the presence of 1% glucose as suppressor of recombinant protein production

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Summary

Introduction

This makes it an ideal reporter for double labeling with green fluorescent protein (GFP). DsRed, has a relatively low emission level and a parasitic green fluorescence peak that cross-talks with GFP emission [4]. Cell Culture and Lysate Preparation—For time course analysis (see Fig. 1C), E. coli carrying EGFP, wild-type DsRed (wtDsRed), or DsRed S197Y in the pET-11 plasmids were grown until OD ϭ 1.0 (at 650 nm) in the presence of 1% glucose as suppressor of recombinant protein production.

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