An improved one-tube RT-PCR protocol for analyzing single-cell gene expression in individual mammalian cells

Yongzhong Li, Hansa Magee, Courtney Hemphill, Fan Hong, Jessica Forrester, Roger H. Johnson, Weiwen Zhang, Deirdre Meldrum

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

It is well known that gene expression is regulated at the level of individual cells, and more evidence is now emerging that heterogeneity of cell regulation is orders of magnitude greater than previously thought. In order to detect meaningful variations in transcription levels, it is necessary to measure gene expression at single cell levels rather than in bulk cells, where individual differences or heterogeneity could be lost. In this work, we report an improved reverse-transcriptase polymerase chain reaction (RT-PCR) protocol which allows the direct measurement of gene expression in one tube (5-25 μl of total PCR mixture) at the single mammalian cell level. The protocol employs a new cell lysis buffer, and involves no RNA isolation or nested PCR steps, significantly reducing the possibility of contamination and errors. We successfully applied this protocol in qRT-PCR and linear-after-the-exponential (LATE)-PCR to analyze selected genes of various expression levels from three cell lines. Although further characterization of RNA stability is important, the preliminary results showed that gene expression heterogeneity could be common among members of genetically identical cell populations. The protocol illustrated can be utilized for a wide array of applications without much modification, such as cancer cell analysis and preimplantation genetic diagnostics. In addition, the protocol is based on intercalator-based (SYBR Green PCR) chemistry, which is less expensive and suitable for high-throughput platforms.

Original languageEnglish (US)
Pages (from-to)1853-1859
Number of pages7
JournalAnalytical and Bioanalytical Chemistry
Volume397
Issue number5
DOIs
StatePublished - Jul 2010

Fingerprint

Polymerase chain reaction
RNA-Directed DNA Polymerase
Reverse Transcriptase Polymerase Chain Reaction
Gene expression
Cells
Gene Expression
Polymerase Chain Reaction
RNA
Intercalating Agents
Transcription
Buffers
Contamination
Genes
Throughput
RNA Stability
Individuality
Cell Line
Population

Keywords

  • Gene expression
  • One-tube
  • RT-PCR
  • Single-cell

ASJC Scopus subject areas

  • Analytical Chemistry
  • Biochemistry

Cite this

An improved one-tube RT-PCR protocol for analyzing single-cell gene expression in individual mammalian cells. / Li, Yongzhong; Magee, Hansa; Hemphill, Courtney; Hong, Fan; Forrester, Jessica; Johnson, Roger H.; Zhang, Weiwen; Meldrum, Deirdre.

In: Analytical and Bioanalytical Chemistry, Vol. 397, No. 5, 07.2010, p. 1853-1859.

Research output: Contribution to journalArticle

Li, Yongzhong ; Magee, Hansa ; Hemphill, Courtney ; Hong, Fan ; Forrester, Jessica ; Johnson, Roger H. ; Zhang, Weiwen ; Meldrum, Deirdre. / An improved one-tube RT-PCR protocol for analyzing single-cell gene expression in individual mammalian cells. In: Analytical and Bioanalytical Chemistry. 2010 ; Vol. 397, No. 5. pp. 1853-1859.
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