High-Throughput Fluorescent Tagging of Full-Length Arabidopsis Gene Products in Planta

Author:

Tian Guo-Wei1,Mohanty Amitabh1,Chary S. Narasimha1,Li Shijun1,Paap Brigitte1,Drakakaki Georgia1,Kopec Charles D.1,Li Jianxiong1,Ehrhardt David1,Jackson David1,Rhee Seung Y.1,Raikhel Natasha V.1,Citovsky Vitaly1

Affiliation:

1. Department of Biochemistry and Cell Biology, State University of New York, Stony Brook, New York 11794–5215 (G.-W.T., B.P., C.D.K., J.L., V.C.); Watson School of Biological Sciences (C.D.K.) and Cold Spring Harbor Laboratory (A.M., D.J.), Cold Spring Harbor, New York 11724; Center for Plant Cell Biology and Department of Botany and Plant Sciences, University of California, Riverside, California 9

Abstract

Abstract We developed a high-throughput methodology, termed fluorescent tagging of full-length proteins (FTFLP), to analyze expression patterns and subcellular localization of Arabidopsis gene products in planta. Determination of these parameters is a logical first step in functional characterization of the approximately one-third of all known Arabidopsis genes that encode novel proteins of unknown function. Our FTFLP-based approach offers two significant advantages: first, it produces internally-tagged full-length proteins that are likely to exhibit native intracellular localization, and second, it yields information about the tissue specificity of gene expression by the use of native promoters. To demonstrate how FTFLP may be used for characterization of the Arabidopsis proteome, we tagged a series of known proteins with diverse subcellular targeting patterns as well as several proteins with unknown function and unassigned subcellular localization.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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