An ORFeome-based analysis of human transcription factor genes and the construction of a microarray to interrogate their expression

Transcription factors (TFs) are essential regulators of gene expression, and mutated TF genes have been shown to cause numerous human genetic diseases. Yet to date, no single, comprehensive database of human TFs exists. In this work, we describe the collection of an essentially complete set of TF ge...

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Bibliographic Details
Published in:Genome research 2004-10, Vol.14 (10B), p.2041-2047
Main Authors: Messina, David N, Glasscock, Jarret, Gish, Warren, Lovett, Michael
Format: Article
Language:English
Subjects:
Gene Expression Profiling
Genome, Human
Humans
Letters
Markov Chains
Oligonucleotide Array Sequence Analysis
Open Reading Frames - genetics
Transcription Factors - chemistry
Transcription Factors - genetics
Transcription Factors - metabolism
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Summary:Transcription factors (TFs) are essential regulators of gene expression, and mutated TF genes have been shown to cause numerous human genetic diseases. Yet to date, no single, comprehensive database of human TFs exists. In this work, we describe the collection of an essentially complete set of TF genes from one depiction of the human ORFeome, and the design of a microarray to interrogate their expression. Taking 1468 known TFs from TRANSFAC, InterPro, and FlyBase, we used this seed set to search the ScriptSure human transcriptome database for additional genes. ScriptSure's genome-anchored transcript clusters allowed us to work with a nonredundant high-quality representation of the human transcriptome. We used a high-stringency similarity search by using BLASTN, and a protein motif search of the human ORFeome by using hidden Markov models of DNA-binding domains known to occur exclusively or primarily in TFs. Four hundred ninety-four additional TF genes were identified in the overlap between the two searches, bringing our estimate of the total number of human TFs to 1962. Zinc finger genes are by far the most abundant family (762 members), followed by homeobox (199 members) and basic helix-loop-helix genes (117 members). We designed a microarray of 50-mer oligonucleotide probes targeted to a unique region of the coding sequence of each gene. We have successfully used this microarray to interrogate TF gene expression in species as diverse as chickens and mice, as well as in humans.
ISSN:1088-9051
1549-5469
DOI:10.1101/gr.2584104