Abstract
Hox genes encode transcription factors that control spatial patterning during embryogenesis. To date, downstream targets of Hox genes have proven difficult to identify. Here, we describe studies designed to identify target genes under the control of the murine transcription factor Hoxc8. We used a mouse 16,463 gene oligonucleotide microarray to identify mRNAs whose expression was altered by the overexpression of Hoxc8 in C57BL/6J mouse embryo fibroblasts (MEF) in cell culture (in vitro). We identified a total of 34 genes whose expression was changed by 2-fold or greater: 16 genes were up-regulated, and 18 genes were down-regulated. The majority of genes encoded proteins involved in critical biological processes, such as cell adhesion, migration, metabolism, apoptosis, and tumorigenesis. Two genes showed high levels of regulation: (i) secreted phosphoprotein 1 (Spp1), also known as osteopontin (OPN), was down-regulated 4.8-fold, and (ii) frizzled homolog 2 (Drosophila) (Fzd2) was up-regulated 4.4-fold. Chromatin immunoprecipitation (ChIP) analysis confirmed the direct interaction between the OPN promoter and Hoxc8 protein in vivo, supporting the view that OPN is a direct transcriptional target of Hoxc8.
MeSH Terms
Animals
Base Sequence
Body Patterning/genetics
Cell Line
DNA Primers/genetics
Gene Expression Profiling
Gene Expression Regulation, Developmental
Genes, Homeobox
Homeodomain Proteins/genetics
Mice
Mice, Inbred C57BL
Oligonucleotide Array Sequence Analysis
Osteopontin
RNA, Messenger/genetics
Reverse Transcriptase Polymerase Chain Reaction
Sialoglycoproteins/genetics
Transfection
Chemicals
DNA Primers
Homeodomain Proteins
Hoxc8 protein, mouse
RNA, Messenger
Sialoglycoproteins
Spp1 protein, mouse
Osteopontin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lei Haiyan
Department of Molecular, Cellular, and Developmental Biology, Yale University, 266 Whitney Avenue, New Haven, CT 06511, USA.
Wang Hailong
Juan Aster H
Ruddle Frank H
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