INSULIN GENE ENHANCER BINDING-PROTEIN ISL-1 IS A MEMBER OF A NOVEL CLASS OF PROTEINS CONTAINING BOTH A HOMEODOMAIN AND A CYS-HIS DOMAIN

被引:650
作者
KARLSSON, O [1 ]
THOR, S [1 ]
NORBERG, T [1 ]
OHLSSON, H [1 ]
EDLUND, T [1 ]
机构
[1] UMEA UNIV,DEPT MICROBIOL,S-90187 UMEA,SWEDEN
关键词
D O I
10.1038/344879a0
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
THE activity of the rat insulin I gene enhancer is mainly dependent on two cis-acting protein-binding domains1-3. Here we report the isolation of a complementary DNA encoding a protein, Isl-1, that binds to one of these domains. Isl-1 contains a homeodomain with greatest similarity to those of the Caenorhabditis elegans proteins encoded by mec-3 (ref. 4) and lin-11 (ref. 5). In addition, Isl-1, like the lin-11 and mec-3 gene products, contains a novel Cys-His domain which is reminiscent of known metal-binding regions. Together these proteins define a novel class of proteins containing both a homeo- and a Cys His-domain. Isl-1 is preferentially expressed in cells of pancreatic endocrine origin. If the structural homologies between Isl-1 and the C. elegans gene products reflect functional similarities, a role for Isl-1 in the development of pancreatic endocrine cells could be envisaged. © 1990 Nature Publishing Group.
引用
收藏
页码:879 / 882
页数:4
相关论文
共 21 条
[1]   HYBRID INSULIN GENES REVEAL A DEVELOPMENTAL LINEAGE FOR PANCREATIC ENDOCRINE-CELLS AND IMPLY A RELATIONSHIP WITH NEURONS [J].
ALPERT, S ;
HANAHAN, D ;
TEITELMAN, G .
CELL, 1988, 53 (02) :295-308
[2]   ONCOGENE JUN ENCODES A SEQUENCE-SPECIFIC TRANS-ACTIVATOR SIMILAR TO AP-1 [J].
ANGEL, P ;
ALLEGRETTO, EA ;
OKINO, ST ;
HATTORI, K ;
BOYLE, WJ ;
HUNTER, T ;
KARIN, M .
NATURE, 1988, 332 (6160) :166-171
[3]  
AUFFRAY C, 1980, EUR J BIOCHEM, V107, P303
[4]   INSULIN, GLUCAGON, AND SOMATOSTATIN RECEPTORS ON CULTURED-CELLS AND CLONES FROM RAT ISLET CELL TUMOR [J].
BHATHENA, SJ ;
OIE, HK ;
GAZDAR, AF ;
VOYLES, NR ;
WILKINS, SD ;
RECANT, L .
DIABETES, 1982, 31 (06) :521-531
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]   BETA-CELL LINES DERIVED FROM TRANSGENIC MICE EXPRESSING A HYBRID INSULIN GENE ONCOGENE [J].
EFRAT, S ;
LINDE, S ;
KOFOD, H ;
SPECTOR, D ;
DELANNOY, M ;
GRANT, S ;
HANAHAN, D ;
BAEKKESKOV, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :9037-9041
[7]   THE STEROID AND THYROID-HORMONE RECEPTOR SUPERFAMILY [J].
EVANS, RM .
SCIENCE, 1988, 240 (4854) :889-895
[8]  
FERGUSON EL, 1987, NATURE, V326, P260
[9]   NOVEL CYSTEINE-RICH MOTIF AND HOMEODOMAIN IN THE PRODUCT OF THE CAENORHABDITIS-ELEGANS CELL LINEAGE GENE LIN-II [J].
FREYD, G ;
KIM, SK ;
HORVITZ, HR .
NATURE, 1990, 344 (6269) :876-879
[10]   INDIVIDUAL PROTEIN-BINDING DOMAINS OF THE INSULIN GENE ENHANCER POSITIVELY ACTIVATE BETA-CELL-SPECIFIC TRANSCRIPTION [J].
KARLSSON, O ;
WALKER, MD ;
RUTTER, WJ ;
EDLUND, T .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (02) :823-827