Issue 13, 2012

Detection of expressed gene in isolated single cells in microchambers by a novel hot cell-direct RT-PCR method

Abstract

In order to be able to detect the expression of a gene in individual cells, the ability to isolate and lyse a single cell and to perform reverse transcription polymerase chain reaction (RT-PCR) in one device is important. As is common, when performing cell lysis and RT-PCR in the same reaction chamber, it is necessary to add the reagent for RT-PCR after cell lysis. In this study, we propose an original formula for cell lysis and RT-PCR in the same reaction chamber without the addition of reagent by only a heat process, which we termed hot cell-direct RT-PCR. Hot cell-direct RT-PCR was enabled by using Tth DNA polymerase, which is a thermostable polymerase and has high reverse transcription activity in the presence of manganese ions. Direct detection of RT-PCR products was performed by detecting fluorescence with the use of a double-dye fluorescent probe. We attempted to detect the mRNA of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene in isolated Jurkat cells on a microfluidic device, which we had already developed for single cell isolation. After cell isolation and successive hot cell-direct RT-PCR on the device, fluorescent signals from RT-PCR products for a single cell were detected and differentiated from the chamber containing no cells. A highly positive linear relationship (r = 0.9933) was observed between the number of chambers containing cell(s) and those containing RT-PCR products from 10 to 400 cells μL−1. Thus it was possible to use the novel hot cell-direct RT-PCR method to detect the expressed gene in isolated cells.

Graphical abstract: Detection of expressed gene in isolated single cells in microchambers by a novel hot cell-direct RT-PCR method

Article information

Article type
Paper
Submitted
16 Sep 2011
Accepted
05 Dec 2011
First published
11 Jan 2012

Analyst, 2012,137, 2951-2957

Detection of expressed gene in isolated single cells in microchambers by a novel hot cell-direct RT-PCR method

S. Furutani, H. Nagai, Y. Takamura, Y. Aoyama and I. Kubo, Analyst, 2012, 137, 2951 DOI: 10.1039/C2AN15866C

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