RNA expression profiling at the single molecule level
Author(s) -
Jürgen Hesse,
Jaroslaw Jacak,
Maria Kasper,
Gerhard Regl,
Thomas Eichberger,
Martina Winklmayr,
Fritz Aberger,
Max Sonnleitner,
Robert Schlapak,
Stefan Howorka,
Leila Mureşan,
AnnaMaria Frischauf,
Gerhard J. Schütz
Publication year - 2006
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.4999906
Subject(s) - biochip , biology , oligonucleotide , gene expression profiling , microbiology and biotechnology , microarray , complementary dna , dna microarray , computational biology , oligomer restriction , gene , microarray analysis techniques , rna , gene expression , genetics
We developed a microarray platform for PCR amplification-independent expression profiling of minute samples. A novel scanning system combined with specialized biochips enables detection down to individual fluorescent oligonucleotide molecules specifically hybridized to their complementary sequence over the entire biochip surface of cm2 size. A detection limit of 1.3 fM target oligonucleotide concentration--corresponding to only 39,000 molecules in the sample solution--and a dynamic range of 4.7 orders of magnitude have been achieved. The applicability of the system to PCR amplification-independent gene-expression profiling of minute samples was demonstrated by complex hybridization of cDNA derived from the equivalent of only 10(4) cells, which matches results obtained in ensemble studies on large samples. By counting each hybridized molecule on the microarray, the method is insusceptible to gene-specific variations of the labeling, thereby representing a principle advance to conventional ensemble-based microarray analysis.
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