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Article
Nature Genetics  27, 392 - 398 (2001)
doi:10.1038/86891

Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31

Jean C. Zenklusen1, Claudio J. Conti2 & Eric D. Green1

1  Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.

2  Department of Carcinogenesis, M.D. Anderson Cancer Center, The University of Texas, Smithville, Texas, USA.

Correspondence should be addressed to Jean C. Zenklusen jcz@nhgri.nih.gov or Eric D. Green egreen@nhgri.nih.gov
Loss of heterozygosity (LOH) of markers on human chromosome 7q31 is frequently encountered in a variety of human neoplasias, indicating the presence of a tumor-suppressor gene (TSG). By a combination of microcell-fusion and deletion-mapping studies, we previously established that this TSG resides within a critical region flanked by the genetic markers D7S522 and D7S677. Using a positional cloning strategy and aided by the availability of near-complete sequence of this genomic interval, we have identified a TSG within 7q31, named ST7 (for suppression of tumorigenicity 7; this same gene was recently reported in another context and called RAY1). ST7 is ubiquitously expressed in human tissues. Analysis of a series of cell lines derived from breast tumors and primary colon carcinomas revealed the presence of mutations in ST7. Introduction of the ST7 cDNA into the prostate-cancer−derived cell line PC3 had no effect on the in vitro proliferation of the cells, but abrogated their in vivo tumorigenicity. Our data indicate that ST7 is a TSG within chromosome 7q31 and may have an important role in the development of some types of human cancer.

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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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