Construction of a consistent YAC contig for human chromosome region 3p14.1.
Author(s) -
Walter Bardenheuer,
S Michaelis,
Andreas Lux,
Lydia Vieten,
Frank Bröcker,
K. Jülicher,
C. Willers,
Reiner Siebert,
Jeremy C. Smith,
Annemarie H. van der Hout,
Charles H.C.M. Buys,
J. Schütte,
Bertram Opalka
Publication year - 1996
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.6.3.176
Subject(s) - contig , biology , yeast artificial chromosome , genetics , positional cloning , locus (genetics) , gene mapping , chromosome , microbiology and biotechnology , fluorescence in situ hybridization , gene , genome
Chromosomal deletions and translocations of human chromosome region 3p14 are observed in various human malignancies and suggest the existence of a tumor suppressor gene locus within this region. Tumors most frequently affected by these aberrations are small-cell lung cancer and renal-cell carcinoma. In continuation of our previously published YAC contig of chromosome region 3p14.2-p14.3, we report here on the construction of a YAC contig of at least 11 Mb that consisted of 171 YACs and covers the entire subregion 3p14.1. This contig includes the t(3;8) breakpoint of a hereditary renal-cell carcinoma localized in 3p14.2 and extends into human chromosome region 3p12-p13. It defines the order of 34 DNA probes in relation to reference markers D3S6 and D3S30 as well as the human protein tyrosine phosphatase-gamma gene. For 31 DNA probes we identified nonchimeric YACs by fluorescence in situ hybridization. The minimal tilling pathway consists of 16 yeast artificial chromosomes. As a prerequisite for identification of a putative tumor suppressor gene within this region, this contig renders human chromosome region 3p14.1 accessible to gene isolation.
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