Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/97387
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Type: Journal article
Title: Protocol: a fast and simple in situ PCR method for localising gene expression in plant tissue
Author: Athman, A.
Tanz, S.
Conn, V.
Jordans, C.
Mayo, G.
Ng, W.
Burton, R.
Conn, S.
Gilliham, M.
Citation: Plant Methods, 2014; 10(1):29-1-29-19
Publisher: BioMed Central
Issue Date: 2014
ISSN: 1746-4811
1746-4811
Statement of
Responsibility: 
Asmini Athman, Sandra K Tanz, Vanessa M Conn, Charlotte Jordans, Gwenda M Mayo, Weng W Ng, Rachel A Burton, Simon J Conn, and Matthew Gilliham
Abstract: BACKGROUND: An important step in characterising the function of a gene is identifying the cells in which it is expressed. Traditional methods to determine this include in situ hybridisation, gene promoter-reporter fusions or cell isolation/purification techniques followed by quantitative PCR. These methods, although frequently used, can have limitations including their time-consuming nature, limited specificity, reliance upon well-annotated promoters, high cost, and the need for specialized equipment. In situ PCR is a relatively simple and rapid method that involves the amplification of specific mRNA directly within plant tissue whilst incorporating labelled nucleotides that are subsequently detected by immunohistochemistry. Another notable advantage of this technique is that it can be used on plants that are not easily genetically transformed. RESULTS: An optimised workflow for in-tube and on-slide in situ PCR is presented that has been evaluated using multiple plant species and tissue types. The protocol includes optimised methods for: (i) fixing, embedding, and sectioning of plant tissue; (ii) DNase treatment; (iii) in situ RT-PCR with the incorporation of DIG-labelled nucleotides; (iv) signal detection using colourimetric alkaline phosphatase substrates; and (v) mounting and microscopy. We also provide advice on troubleshooting and the limitations of using fluorescence as an alternative detection method. Using our protocol, reliable results can be obtained within two days from harvesting plant material. This method requires limited specialized equipment and can be adopted by any laboratory with a vibratome (vibrating blade microtome), a standard thermocycler, and a microscope. We show that the technique can be used to localise gene expression with cell-specific resolution. CONCLUSIONS: The in situ PCR method presented here is highly sensitive and specific. It reliably identifies the cellular expression pattern of even highly homologous and low abundance transcripts within target tissues, and can be completed within two days of harvesting tissue. As such, it has considerable advantages over other methods, especially in terms of time and cost. We recommend its adoption as the standard laboratory technique of choice for demonstrating the cellular expression pattern of a gene of interest.
Keywords: Cell-specific localisation; Immunohistochemistry; In situ PCR; Plant tissue; RT-PCR
Rights: © Athman et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​4.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
RMID: 0030015404
DOI: 10.1186/1746-4811-10-29
Grant ID: http://purl.org/au-research/grants/arc/DP130104205
http://purl.org/au-research/grants/arc/FT130100709
http://purl.org/au-research/grants/arc/CE140100008
http://purl.org/au-research/grants/arc/DE120100307
Appears in Collections:Agriculture, Food and Wine publications

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