An optimised direct lysis method for gene expression studies on low cell numbers

• Published in: Scientific reports Vol. 5; no. 1; p. 12859
• Main Authors: Le, Anh Viet-Phuong, Huang, Dexing, Blick, Tony, Thompson, Erik W, Dobrovic, Alexander
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 05.08.2015
• Subjects: Bovine serum albumin; Breast cancer; Cell Fractionation; Cell Line, Tumor; Gene Expression; Gene Expression Profiling - methods; Humans; Lysis; Polymerase chain reaction; Reverse transcription; Ribonucleic acid; RNA; RNA - genetics; RNA - isolation & purification; RNA - metabolism; Transcriptome; Tumor cell lines; Tumors
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep12859

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.