Abstract
We have developed an automated, high-throughput, systematic cDNA display method called TOGA, an acronym for total gene expression analysis. TOGA utilizes 8-nt sequences, comprised of a 4-nt restriction endonuclease cleavage site and adjacent 4-nt parsing sequences, and their distances from the 3' ends of mRNA molecules to give each mRNA species in an organism a single identity. The parsing sequences are used as parts of primer-binding sites in 256 PCR-based assays performed robotically on tissue extracts to determine simultaneously the presence and relative concentration of nearly every mRNA in the extracts, regardless of whether the mRNA has been discovered previously. Visualization of the electrophoretically separated fluorescent assay products from different extracts displayed via a Netscape browser-based graphical user interface allows the status of each mRNA to be compared among samples and its identity to be matched with sequences of known mRNAs compiled in databases.
MeSH Terms
Automation
Base Sequence
DNA-Binding Proteins/genetics
Gene Expression Profiling
Humans
Molecular Sequence Data
NF-kappa B/genetics
Nuclear Receptor Subfamily 4, Group A, Member 2
RNA, Messenger/analysis
Reproducibility of Results
Sensitivity and Specificity
Software
Transcription Factors/genetics
Chemicals
DNA-Binding Proteins
NF-kappa B
NR4A2 protein, human
Nuclear Receptor Subfamily 4, Group A, Member 2
RNA, Messenger
Transcription Factors
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Sutcliffe J G
Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
[email protected]
Foye P E
Erlander M G
Hilbush B S
Bodzin L J
Durham J T
Hasel K W
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