FINE MAPPING OF PROBES IN THE ADENOMATOUS POLYPOSIS-COLI REGION OF CHROMOSOME-5 BY INSITU HYBRIDIZATION

被引:21
作者
WILLIAMS, SV
JONES, TA
COTTRELL, S
ZEHETNER, G
VARESCO, L
WARD, T
THOMAS, H
LAWSON, PA
SOLOMON, E
BODMER, WF
FRISCHAUF, AM
SHEER, D
机构
[1] IMPERIAL CANC RES FUND,HUMAN CYTOGENET LAB,POB 123,LINCOLNS INN FIELDS,LONDON WC2A 3PX,ENGLAND
[2] IMPERIAL CANC RES FUND,MOLEC ANAL MAMMALIAN MUTAT LAB,LONDON WC2A 3PX,ENGLAND
[3] IMPERIAL CANC RES FUND,DIRECTORS LAB,LONDON WC2A 3PX,ENGLAND
[4] IMPERIAL CANC RES FUND,GENOME ANAL LAB,LONDON WC2A 3PX,ENGLAND
[5] IMPERIAL CANC RES FUND,SOMAT CELL GENET LAB,LONDON WC2A 3PX,ENGLAND
关键词
D O I
10.1002/gcc.2870030509
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The gene for adenomatous polyposis coli has been localized to 5q21-22. We have mapped six probes from this region using isotopic or nonisotopic in situ hybridization. Using tritium-labeled probes we localized PI-227 (D5S37) to 5q14-15 and ECB27 (D5S98) to 5q21. Following hybridization with biotin-labeled probes, the positions of signals along the chromosomes were measured as fractional length relative to the length of the chromosome arm from centromers to qter (FLcen-qter). Ninety-five percent confidence limits, compared with standard karyotypes, provided the corresponding band localization. By this method we localized C11p11 (D5S71) to FLcen-qter 0.407-0.452 (5q21.1-21.3), ECB27 to FLcen-qter 0.426-0.473 (5q21.3), YN5.48 (D5s81) to FLcen-qter 0.459-0.496 (5q21.3-22.2), and ECB134 (D5S97) to FLcen-qter 0.509-0.533 (5q22.3-23.1). ECB220 had three sites of hybridization, a major site at FLcen-qter 0.460-0.492 (5q21.3-22.1) and minor sites at FLcen-qter 0.299-0.339 (5q14.3-15) and FLcen-qter 0.629-0.691 (5q23.3-31.2). We have shown that the chromosome 5 breakpoint in a t(5;15) translocation from a patient with Gardner's syndrome (GM03314) is between C11p11 and ECB27. Linkage data are presented suggesting that ECB27 is located on the same side of the APC locus as PI-227. These and published results including data on several constitutional deletions (M, SD, and brothers PW and ND) give a probable order of [cen] - [PI-227, proximal SD breakpoint] - [C11p11] - [proximal PW/ND, M breakpoint(s), GM03314 breakpoint] - [ECB27] - [APC] - [YN5.48] - [distal PW/ND breakpoint] - [ECB134] - [distal M breakpoint] - [qter]. The major site of ECB220 appears to be between ECB27 and the distal PW/ND breakpoint; the distal SD breakpoint is distal to YN5.48.
引用
收藏
页码:382 / 389
页数:8
相关论文
共 29 条
[11]   CLOSE LINKAGE OF A HIGHLY POLYMORPHIC MARKER (D5S37) TO FAMILIAL ADENOMATOUS POLYPOSIS (FAP) AND CONFIRMATION OF FAP LOCALIZATION ON CHROMOSOME 5Q21-Q22 [J].
KHAN, PM ;
TOPS, CMJ ;
BREUKEL, C ;
WIJNEN, JT ;
OLDENBURG, M ;
VANLEEUWENCORNELISSE, ISJ ;
VASEN, HFA ;
GRIFFIOEN, G ;
VERSPAGET, HM ;
DENHARTOGJAGER, FCA ;
LAMERS, CBHW ;
VANDERBROEK, M ;
VANDERBOS, J .
HUMAN GENETICS, 1988, 79 (02) :183-185
[12]   USE OF WHOLE COSMID CLONED GENOMIC SEQUENCES FOR CHROMOSOMAL LOCALIZATION BY NON-RADIOACTIVE INSITU HYBRIDIZATION [J].
LANDEGENT, JE ;
DEWAL, NJI ;
DIRKS, RW ;
BAAS, F ;
VANDERPLOEG, M .
HUMAN GENETICS, 1987, 77 (04) :366-370
[13]  
LATHROP GM, 1985, AM J HUM GENET, V37, P482
[14]   INTERPHASE AND METAPHASE RESOLUTION OF DIFFERENT DISTANCES WITHIN THE HUMAN DYSTROPHIN GENE [J].
LAWRENCE, JB ;
SINGER, RH ;
MCNEIL, JA .
SCIENCE, 1990, 249 (4971) :928-932
[15]   THE GENE FOR FAMILIAL POLYPOSIS-COLI MAPS TO THE LONG ARM OF CHROMOSOME-5 [J].
LEPPERT, M ;
DOBBS, M ;
SCAMBLER, P ;
OCONNELL, P ;
NAKAMURA, Y ;
STAUFFER, D ;
WOODWARD, S ;
BURT, R ;
HUGHES, J ;
GARDNER, E ;
LATHROP, M ;
WASMUTH, J ;
LALOUEL, JM ;
WHITE, R .
SCIENCE, 1987, 238 (4832) :1411-1413
[16]   GENETIC-ANALYSIS OF AN INHERITED PREDISPOSITION TO COLON CANCER IN A FAMILY WITH A VARIABLE NUMBER OF ADENOMATOUS POLYPS [J].
LEPPERT, M ;
BURT, R ;
HUGHES, JP ;
SAMOWITZ, W ;
NAKAMURA, Y ;
WOODWARD, S ;
GARDNER, E ;
LALOUEL, JM ;
WHITE, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (13) :904-908
[17]   HIGH-RESOLUTION MAPPING OF HUMAN CHROMOSOME-11 BY INSITU HYBRIDIZATION WITH COSMID CLONES [J].
LICHTER, P ;
TANG, CJC ;
CALL, K ;
HERMANSON, G ;
EVANS, GA ;
HOUSMAN, D ;
WARD, DC .
SCIENCE, 1990, 247 (4938) :64-69
[18]  
LINDGREN V, 1989, American Journal of Human Genetics, V45, pA81
[19]  
MURDAY V, 1989, CYTOGENET CELL GENET, V51, P1049
[20]  
NAKAMURA Y, 1988, AM J HUM GENET, V43, P638