scispace - formally typeset
Open AccessJournal ArticleDOI

Tape-Arabidopsis Sandwich - a simpler Arabidopsis protoplast isolation method

TLDR
The protoplasts generated by this new Tape-Arabidopsis Sandwich method are suitable for the same range of research applications as those that use the current method, but require less operator skill, equipment and time.
Abstract
Protoplasts isolated from leaves are useful materials in plant research. One application, the transient expression of recombinant genes using Arabidopsis mesophyll protoplasts (TEAMP), is currently commonly used for studies of subcellular protein localization, promoter activity, and in vivo protein-protein interactions. This method requires cutting leaves into very thin slivers to collect mesophyll cell protoplasts, a procedure that often causes cell damage, may yield only a few good protoplasts, and is time consuming. In addition, this protoplast isolation method normally requires a large number of leaves derived from plants grown specifically under low-light conditions, which may be a concern when material availability is limited such as with mutant plants, or in large scale experiments. In this report, we present a new procedure that we call the Tape-Arabidopsis Sandwich. This is a simple and fast mesophyll protoplast isolation method. Two kinds of tape (Time tape adhered to the upper epidermis and 3 M Magic tape to the lower epidermis) are used to make a "Tape-Arabidopsis Sandwich". The Time tape supports the top side of the leaf during manipulation, while tearing off the 3 M Magic tape allows easy removal of the lower epidermal layer and exposes mesophyll cells to cell wall digesting enzymes when the leaf is later incubated in an enzyme solution. The protoplasts released into solution are collected and washed for further use. For TEAMP, plasmids carrying a gene expression cassette for a fluorescent protein can be successfully delivered into protoplasts isolated from mature leaves grown under optimal conditions. Alternatively, these protoplasts may be used for bimolecular fluorescence complementation (BiFC) to investigate protein-protein interactions in vivo, or for Western blot analysis. A significant advantage of this protocol over the current method is that it allows the generation of protoplasts in less than 1 hr, and allows TEAMP transfection to be carried out within 2 hr. The protoplasts generated by this new Tape-Arabidopsis Sandwich method are suitable for the same range of research applications as those that use the current method, but require less operator skill, equipment and time.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Interaction between BZR1 and PIF4 integrates brassinosteroid and environmental responses

TL;DR: It is shown that direct interaction between the dark- and heat-activated transcription factor phytochrome-interacting factor 4 (PIF4) and the BR- activated transcription factor BZR1 integrates the hormonal and environmental signals, enabling plant growth co-regulation by the steroid and environmental messages.
Journal ArticleDOI

Brassinosteroid, gibberellin and phytochrome impinge on a common transcription module in Arabidopsis.

TL;DR: It is shown that BR and GA act interdependently through a direct interaction between the BR-activated BZR1 and GA-inactivated DELLA transcription regulators, which defines a core transcription module that mediates coordinated growth regulation by GA, BR and light signals.
Journal ArticleDOI

Opposite Roles of Salicylic Acid Receptors NPR1 and NPR3/NPR4 in Transcriptional Regulation of Plant Immunity

TL;DR: This study indicates that both NPR1 and NPR3/NPR4 are bona fide SA receptors, but play opposite roles in transcriptional regulation of SA-induced defense gene expression.
Journal ArticleDOI

Flexible and Adhesive Surface Enhance Raman Scattering Active Tape for Rapid Detection of Pesticide Residues in Fruits and Vegetables.

TL;DR: A proof-of-concept surface enhance Raman scattering (SERS) active substrate serving directly to the rapid extraction and detection of target molecules is proposed and obtained strong and easily distinguishable SERS signals allow us to detect various pesticide residues in the real samples with complex surfaces.
Journal ArticleDOI

Vacuolar membrane transporters OsVIT1 and OsVIT2 modulate iron translocation between flag leaves and seeds in rice

TL;DR: Interestingly, functional disruption of OsVIT1 andOsVIT2 leads to increased Fe/Zn accumulation in rice seeds and a corresponding decrease in the source organ flag leaves, indicating an enhanced Fe-Zn translocation between source and sink organs, which might represent a novel strategy to biofortify Fe/ Zn in staple foods.
References
More filters
Journal ArticleDOI

Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis.

TL;DR: The transient gene expression system using Arabidopsis mesophyll protoplasts has proven an important and versatile tool for conducting cell-based experiments using molecular, cellular, biochemical, genetic, genomic and proteomic approaches to analyze the functions of diverse signaling pathways and cellular machineries.
Journal ArticleDOI

A multicolored set of in vivo organelle markers for co-localization studies in Arabidopsis and other plants.

TL;DR: In this paper, a series of fluorescent organelle markers based on well-established targeting sequences that can be used for co-localization studies was generated for the Arabidopsis organelle marker set.
Journal ArticleDOI

Visualization of Interactions among bZIP and Rel Family Proteins in Living Cells Using Bimolecular Fluorescence Complementation

TL;DR: Results attest to the general applicability of the BiFC assay for studies of protein interactions.
Journal ArticleDOI

Visualization of protein interactions in living plant cells using bimolecular fluorescence complementation.

TL;DR: The implementation of a bimolecular fluorescence complementation technique for visualization of protein-protein interactions in plant cells revealed a remarkable signal fluorescence intensity of interacting protein complexes as well as a high reproducibility and technical simplicity of the method in different plant systems.
Journal ArticleDOI

Simultaneous visualization of multiple protein interactions in living cells using multicolor fluorescence complementation analysis.

TL;DR: A bimolecular fluorescence complementation approach for the simultaneous visualization of multiple protein interactions in the same cell based on complementation between fragments of fluorescent proteins with different spectral characteristics is described.
Related Papers (5)