TY - JOUR
T1 - The isolation of a yeast artificial chromosome (YAC) contig extending for 2 megabases in the vicinity of the von hippel lindau disease gene
AU - Liu, Wanguo
AU - Plechockl, Marie
AU - Shridhar, Viji
AU - Lyles, Gregory
AU - Song, Zheng
AU - Nakamura, Yasuke
AU - Drabkin, Harry
AU - Vance, Jeffrey
AU - Smith, David I.
N1 - Funding Information:
This work was supported by NIH Grant CA48035 and March of Dimes Basic Research Grant # 1-1227 (to D.I.S.), and NIH Gram HGOO358 (to H.D.). W.L. was supported by a Rumble Fellowship from Wayne State University.
PY - 1993/8
Y1 - 1993/8
N2 - Von Hippel LIndau disease (VHL) is a rare autosomal dominant disease associated with tumors and cysts in multiple organ systems. The VHL disease gene is tightly linked to the polymorphic DNA marker 233E2 (D3S720) and flanked by 479H4 (D3S719) on its telomeric and RAF1 on its centromeric side. Two additional markers, D3S1038 and D3S601, have also been identified, and these markers, like D3S720, are very tightly linked to VHL. Previously 93 cosmid clones were mapped to the larger region, 3p24.2 - pter, surrounding the VHL disease gene (1). Using a Southern-based screening strategy on pools of YAC clones we have Isolated a contig of overlapping YAC clones that extends about 0.7 megabase centromeric, and about 1.3 megabases telomeric of D3S720 and contains all three tightly linked VHL markers. Individual YACs In this contig were hybridized to grids containing cosmids localized between 3p24.2-pter and to several cosmids localized by fluorescent in situ hybridization (FISH) to 3p25. A total of 28 cosmids were positioned on this contig of overlapping YAC clones. We have also identified homologous YAC clones to many additional cosmid clones localized between 3p24.2-p25, although these have not yet been precisely localized relative to the contig of YAC clones. This contig of YAC clones probably contains the VHL disease gene and should facilitate the isolation and characterization of this gene.
AB - Von Hippel LIndau disease (VHL) is a rare autosomal dominant disease associated with tumors and cysts in multiple organ systems. The VHL disease gene is tightly linked to the polymorphic DNA marker 233E2 (D3S720) and flanked by 479H4 (D3S719) on its telomeric and RAF1 on its centromeric side. Two additional markers, D3S1038 and D3S601, have also been identified, and these markers, like D3S720, are very tightly linked to VHL. Previously 93 cosmid clones were mapped to the larger region, 3p24.2 - pter, surrounding the VHL disease gene (1). Using a Southern-based screening strategy on pools of YAC clones we have Isolated a contig of overlapping YAC clones that extends about 0.7 megabase centromeric, and about 1.3 megabases telomeric of D3S720 and contains all three tightly linked VHL markers. Individual YACs In this contig were hybridized to grids containing cosmids localized between 3p24.2-pter and to several cosmids localized by fluorescent in situ hybridization (FISH) to 3p25. A total of 28 cosmids were positioned on this contig of overlapping YAC clones. We have also identified homologous YAC clones to many additional cosmid clones localized between 3p24.2-p25, although these have not yet been precisely localized relative to the contig of YAC clones. This contig of YAC clones probably contains the VHL disease gene and should facilitate the isolation and characterization of this gene.
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U2 - 10.1093/hmg/2.8.1177
DO - 10.1093/hmg/2.8.1177
M3 - Article
C2 - 8104627
AN - SCOPUS:0027325842
SN - 0964-6906
VL - 2
SP - 1177
EP - 1182
JO - Human Molecular Genetics
JF - Human Molecular Genetics
IS - 8
ER -