Cloning of two candidate tumor suppressor genes within a 10 kb region on chromosome 13q14, frequently deleted in chronic lymphocytic leukemia

被引:153
作者
Liu, Y
Corcoran, M
Rasool, O
Ivanova, G
Ibbotson, R
Grander, D
Iyengar, A
Baranova, A
Kashuba, V
Merup, M
Wu, XS
Gardiner, A
Mullenbach, R
Poltaraus, A
Hultstrom, AL
Juliusson, G
Chapman, R
Tiller, M
Cotter, F
Gahrton, G
Yankovsky, N
Zabarovsky, E
Einhorn, S
Oscier, D
机构
[1] KAROLINSKA HOSP,RADIUMHEMMET,S-17176 STOCKHOLM,SWEDEN
[2] ROYAL BOURNEMOUTH HOSP,MOL BIOL LAB,BOURNEMOUTH BH7 7DW,DORSET,ENGLAND
[3] RUSSIAN ACAD SCI,INST GEN GENET,GENOME ANAL LAB,MOSCOW 117809,RUSSIA
[4] KAROLINSKA INST,MOL & TUMOR BIOL CTR,S-17177 STOCKHOLM,SWEDEN
[5] HUDDINGE HOSP,DEPT HEMATOL,S-14186 HUDDINGE,SWEDEN
[6] HUDDINGE HOSP,DEPT MED,S-14186 HUDDINGE,SWEDEN
[7] ICRF,MOL ONCOL UNIT,INST CHILD HLTH,LONDON,ENGLAND
[8] RUSSIAN ACAD SCI,VA ENGELHARDT MOL BIOL INST,DEPT SEQUENCING & MAPPING HUMAN GENOME,MOSCOW 117984,RUSSIA
[9] LINKOPING UNIV HOSP,DEPT HEMATOL,S-58185 LINKOPING,SWEDEN
关键词
chronic lymphocytic leukemia; 13q14; tumor suppressor gene;
D O I
10.1038/sj.onc.1201643
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous studies have indicated the presence of a putative tumor suppressor gene on chromosome 13q14, commonly deleted in patients with B-cell chronic lymphocytic leukemia (B-CLL), We have previously defined a minimally deleted region of 130 kb centromeric to the marker D13S272, and constructed a PAC and cosmid contig encompassing this area, In the present study we have made a detailed restriction and transcriptional map of the region of interest, Using these tools we have screened a panel of 206 primary CLL clones and three cell lines. In five CLL cases we found limited deletions defining the region of interest to an area of no more than 10 kb, Two adjacent genes, termed Leu1 and Leu2 (leukemia-associated gene 1 and 2), mere mapped to the minimally deleted region, with several patients showing deletion borders within these genes, The Leu1 and Lead genes show little homology to previously published genes at the nucleotide and expected translated amino acid sequence level, Mutational analysis of the Leu1 and 2 genes in 170 CLL samples revealed no small intragenic mutations or point mutations, However, in all cases of 13q14 loss examined, the first exon of both genes, which are only 300 bp apart, were deleted, We conclude that the Leu1 and Lead genes are strong candidates as tumor suppressor gene(s) involved in B-CLL leukemogenesis.
引用
收藏
页码:2463 / 2473
页数:11
相关论文
共 39 条
[1]   NOTI LINKING CLONES AS A TOOL FOR JOINING PHYSICAL AND GENETIC MAPS OF THE HUMAN GENOME [J].
ALLIKMETS, RL ;
KASHUBA, VI ;
PETTERSSON, B ;
GIZATULLIN, R ;
LEBEDEVA, T ;
KHOLODNYUK, ID ;
BANNIKOV, VM ;
PETROV, N ;
ZAKHARYEV, VM ;
WINBERG, G ;
MODI, W ;
DEAN, M ;
UHLEN, M ;
KISSELEV, LL ;
KLEIN, G ;
ZABAROVSKY, ER .
GENOMICS, 1994, 19 (02) :303-309
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]  
Batova A, 1997, CANCER RES, V57, P832
[4]   EVIDENCE FOR A NEW TUMOR SUPPRESSOR LOCUS (DBM) IN HUMAN B-CELL NEOPLASIA TELOMERIC TO THE RETINOBLASTOMA GENE [J].
BROWN, AG ;
ROSS, FM ;
DUNNE, EM ;
STEEL, CM ;
WEIRTHOMPSON, EM .
NATURE GENETICS, 1993, 3 (01) :67-72
[5]  
CORCORAN MM, 1997, IN PRESS BLOOD
[6]   IRREVERSIBLE REPRESSION OF DNA-SYNTHESIS IN FANCONI-ANEMIA CELLS IS ALLEVIATED BY THE PRODUCT OF A NOVEL CYCLIN-RELATED GENE [J].
DIGWEED, M ;
GUNTHERT, U ;
SCHNEIDER, R ;
SEYSCHAB, H ;
FRIEDL, R ;
SPERLING, K .
MOLECULAR AND CELLULAR BIOLOGY, 1995, 15 (01) :305-314
[7]  
FISHER SG, 1994, GENOMICS, V21, P525
[8]  
FROHMAN MA, 1988, P NATL ACAD SCI USA, V85, P8898
[9]  
FU TB, 1994, CANCER RES, V54, P6297
[10]  
GarciaMarco JA, 1996, BLOOD, V88, P1568