IDENTIFICATION OF THE VONHIPPEL-LINDAU DISEASE TUMOR-SUPPRESSOR GENE

被引:2303
作者
LATIF, F
TORY, K
GNARRA, J
YAO, M
DUH, FM
ORCUTT, ML
STACKHOUSE, T
KUZMIN, I
MODI, W
GEIL, L
SCHMIDT, L
ZHOU, FW
LI, H
WEI, MH
CHEN, F
GLENN, G
CHOYKE, P
WALTHER, MM
WENG, YK
DUAN, DSR
DEAN, M
GLAVAC, D
RICHARDS, FM
CROSSEY, PA
FERGUSONSMITH, MA
LEPASLIER, D
CHUMAKOV, I
COHEN, D
CHINAULT, AC
MAHER, ER
LINEHAN, WM
ZBAR, B
LERMAN, MI
机构
[1] UNIV CAMBRIDGE,DEPT PATHOL,CAMBRIDGE CB2 1QP,ENGLAND
[2] NCI,FREDERICK CANC RES & DEV CTR,IMMUNOBIOL LAB,FREDERICK,MD 21702
[3] NCI,FREDERICK CANC RES & DEV CTR,PROGRAM RESOURCES INC DYNCORP,FREDERICK,MD 21702
[4] NCI,SURG BRANCH,BETHESDA,MD 20892
[5] NCI,CANC DIAG BRANCH,BETHESDA,MD 20892
[6] NCI,DEPT RADIOL,CTR CLIN,BETHESDA,MD 20892
[7] NCI,FREDERICK CANC RES & DEV CTR,VIRAL CARCINOGENESIS LAB,FREDERICK,MD 21702
[8] CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
[9] BAYLOR COLL MED,INST MOLEC GENET,HOUSTON,TX 77030
关键词
D O I
10.1126/science.8493574
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A gene discovered by positional cloning has been identified as the von Hippel-Lindau (VHL) disease tumor suppressor gene. A restriction fragment encompassing the gene showed rearrangements in 28 of 221 VHL kindreds. Eighteen of these rearrangements were due to deletions in the candidate gene, including three large nonoverlapping deletions. Intragenic mutations were detected in cell lines derived from VHL patients and from sporadic renal cell carcinomas. The VHL gene is evolutionarily conserved and encodes two widely expressed transcripts of approximately 6 and 6.5 kilobases. The partial sequence of the inferred gene product shows no homology to other proteins, except for an acidic repeat domain found in the procyclic surface membrane glycoprotein of Trypanosoma brucei.
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收藏
页码:1317 / 1320
页数:4
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