Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/17634
Title: An optimised direct lysis method for gene expression studies on low cell numbers.
Authors: Le, Anh Viet-Phuong;Huang, Dexing;Blick, Tony;Thompson, Erik W;Dobrovic, Alexander
Affiliation: University of Melbourne Department of Surgery, St Vincent's Hospital, Melbourne, Victoria, Australia
Translational Genomics & Epigenomics, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia
Institute of Health and Biomedical Innovation and School of Biomedical Sciences, Queensland University of Technology, Brisbane, Queensland, Australia
St. Vincent's Institute, Melbourne, Victoria, Australia
Department of Pathology, University of Melbourne, Melbourne, Victoria, Australia
School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia
Issue Date: 5-Aug-2015
EDate: 2015-08-05
Citation: Scientific reports 2015; 5: 12859
Abstract: There is increasing interest in gene expression analysis of either single cells or limited numbers of cells. One such application is the analysis of harvested circulating tumour cells (CTCs), which are often present in very low numbers. A highly efficient protocol for RNA extraction, which involves a minimal number of steps to avoid RNA loss, is essential for low input cell numbers. We compared several lysis solutions that enable reverse transcription (RT) to be performed directly on the cell lysate, offering a simple rapid approach to minimise RNA loss for RT. The lysis solutions were assessed by reverse transcription quantitative polymerase chain reaction (RT-qPCR) in low cell numbers isolated from four breast cancer cell lines. We found that a lysis solution containing both the non-ionic detergent (IGEPAL CA-630, chemically equivalent to Nonidet P-40 or NP-40) and bovine serum albumin (BSA) gave the best RT-qPCR yield. This direct lysis to reverse transcription protocol outperformed a column-based extraction method using a commercial kit. This study demonstrates a simple, reliable, time- and cost-effective method that can be widely used in any situation where RNA needs to be prepared from low to very low cell numbers.
URI: http://ahro.austin.org.au/austinjspui/handle/1/17634
DOI: 10.1038/srep12859
ORCID: 0000-0003-3414-112X
PubMed URL: 26242641
Type: Journal Article
Research Support, Non-U.S. Gov't
Appears in Collections:Journal articles

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