Epithelial expression and chromosomal location of human TLE genes: Implications for notch signaling and neoplasia

被引:56
作者
Liu, YL
Dehni, G
Purcell, KJ
Sokolow, J
Carcangiu, ML
ArtavanisTsakonas, S
Stifani, S
机构
[1] MCGILL UNIV,MONTREAL NEUROL INST,MONTREAL,PQ H3A 2B4,CANADA
[2] YALE UNIV,SCH MED,DEPT PATHOL,NEW HAVEN,CT 06536
[3] YALE UNIV,SCH MED,HOWARD HUGHES MED INST,BOYER CTR MOLEC MED,DEPT CELL BIOL,NEW HAVEN,CT 06536
[4] YALE UNIV,SCH MED,HOWARD HUGHES MED INST,BOYER CTR MOLEC MED,DEPT BIOL,NEW HAVEN,CT 06536
关键词
D O I
10.1006/geno.1996.0009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The TLE genes are the human homologues of Drosophila groucho, a member of the Notch signaling pathway. This pathway controls a number of different cell-fate choices in invertebrates and vertebrates. We are interested in investigating the functions of the TLE gene family during epithelial determination and carcinogenesis. We show that expression of individual TLE genes correlates with immature epithelial cells that are progressing toward their terminally differentiated state, suggesting a role during epithelial differentiation. In both normal tissues and conditions resulting from incorrect or incomplete maturation events, such as metaplastic and neoplastic transformations, TLE expression is elevated and coincides with Notch expression, implicating these molecules in the maintenance of the undifferentiated state in epithelial cells. We also show that TLE1 and TLE2 are organized in a tandem array at chromosomal location 19p13.3, while TLE3 maps to 15q22. (C) 1996 Academic Press, Inc.
引用
收藏
页码:58 / 64
页数:7
相关论文
共 26 条
[1]   NOTCH SIGNALING [J].
ARTAVANISTSAKONAS, S ;
MATSUNO, K ;
FORTINI, ME .
SCIENCE, 1995, 268 (5208) :225-232
[2]  
Costarelis G, 1990, CELL, V61, P1329
[3]  
DEHNI G, 1995, MECH DEVELOP, V53, P1
[4]   TAN-1, THE HUMAN HOMOLOG OF THE DROSOPHILA NOTCH GENE, IS BROKEN BY CHROMOSOMAL TRANSLOCATIONS IN T-LYMPHOBLASTIC NEOPLASMS [J].
ELLISEN, LW ;
BIRD, J ;
WEST, DC ;
SORENG, AL ;
REYNOLDS, TC ;
SMITH, SD ;
SKLAR, J .
CELL, 1991, 66 (04) :649-661
[5]   AN ACTIVATED NOTCH RECEPTOR BLOCKS CELL-FATE COMMITMENT IN THE DEVELOPING DROSOPHILA EYE [J].
FORTINI, ME ;
REBAY, I ;
CARON, LA ;
ARTAVANISTSAKONAS, S .
NATURE, 1993, 365 (6446) :555-557
[6]   THE SECRET LIFE OF THE HAIR FOLLICLE [J].
HARDY, MH .
TRENDS IN GENETICS, 1992, 8 (02) :55-61
[7]   A DEDUCED GENE-PRODUCT FROM THE DROSOPHILA NEUROGENIC LOCUS, ENHANCER OF SPLIT, SHOWS HOMOLOGY TO MAMMALIAN G-PROTEIN BETA-SUBUNIT [J].
HARTLEY, DA ;
PREISS, A ;
ARTAVANISTSAKONAS, S .
CELL, 1988, 55 (05) :785-795
[8]   EXPRESSION OF AN ACTIVATED NOTCH-RELATED INT-3 TRANSGENE INTERFERES WITH CELL-DIFFERENTIATION AND INDUCES NEOPLASTIC TRANSFORMATION IN MAMMARY AND SALIVARY-GLANDS [J].
JHAPPAN, C ;
GALLAHAN, D ;
STAHLE, C ;
CHU, E ;
SMITH, GH ;
MERLINO, G ;
CALLAHAN, R .
GENES & DEVELOPMENT, 1992, 6 (03) :345-355
[9]   STEM-CELL PATTERNING AND FATE IN HUMAN EPIDERMIS [J].
JONES, PH ;
HARPER, S ;
WATT, FM .
CELL, 1995, 80 (01) :83-93
[10]   MOUSE NOTCH - EXPRESSION IN HAIR-FOLLICLES CORRELATES WITH CELL FATE DETERMINATION [J].
KOPAN, R ;
WEINTRAUB, H .
JOURNAL OF CELL BIOLOGY, 1993, 121 (03) :631-641