THE IKAROS GENE ENCODES A FAMILY OF FUNCTIONALLY DIVERSE ZINC-FINGER DNA-BINDING PROTEINS

被引:385
作者
MOLNAR, A [1 ]
GEORGOPOULOS, K [1 ]
机构
[1] HARVARD UNIV, MASSACHUSETTS GEN HOSP, SCH MED, CUTANEOUS BIOL RES CTR, BOSTON, MA 02129 USA
关键词
D O I
10.1128/MCB.14.12.8292
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
We previously described the lymphocyte-restricted Ikaros gene encoding a zinc finger DNA-binding protein as a potential regulator of lymphocyte commitment and differentiation. Here, we report the isolation of four additional Ikaros transcripts, products of alternate splicing that encode functionally diverse proteins. The Ikaros proteins contain unique combinations of zinc finger modules that dictate their overall sequence specificity and affinity. The Ik-1 and Ik-2 proteins can both bind, albeit with different affinities, to the same recognition sequences present in a number of lymphocyte-specific regulatory elements. The Ik-3 and the Ik-4 proteins interact only with a subset of these motifs. The Ik-1 and Ik-2 proteins can strongly stimulate transcription, whereas Ik-3 and Ik-4 are weak activators. Significantly, the transcription activation potential of the Ikaros proteins correlates with their subcellular localization. Upon ectopic expression of the Ikaros isoforms in nonlymphoid cells, Ik-1 and Ik-2 localize to the nucleus, whereas Ik-3 and Ik-4 are predominantly found in the cytoplasm. The Ikaros isoforms are expressed differentially in lymphocytes: Ik-1 and Ik-2 mRNAs are the predominating forms, and Ik-4 is present in significant amounts only in early T-cell progenitors, whereas Ik-3 and Ik-5 transcripts are expressed at relatively low levels throughout lymphocyte development. The ability of the Ikaros gene to generate functionally diverse proteins that may participate in distinct regulatory pathways substantiates its role as a master regulator during lymphocyte development.
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页码:8292 / 8303
页数:12
相关论文
共 49 条
[1]   PAX-5 ENCODES THE TRANSCRIPTION FACTOR BSAP AND IS EXPRESSED IN LYMPHOCYTES-B, THE DEVELOPING CNS, AND ADULT TESTIS [J].
ADAMS, B ;
DORFLER, P ;
AGUZZI, A ;
KOZMIK, Z ;
URBANEK, P ;
MAURERFOGY, I ;
BUSSLINGER, M .
GENES & DEVELOPMENT, 1992, 6 (09) :1589-1607
[2]   PERFORMANCE OF AN AUTOMATED-SYSTEM FOR CAPILLARY MICROINJECTION INTO LIVING CELLS [J].
ANSORGE, W ;
PEPPERKOK, R .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1988, 16 (04) :283-292
[3]   BINDING OF A NUCLEAR FACTOR TO A REGULATORY SEQUENCE IN THE PROMOTER OF THE MOUSE H-2KB CLASS-I MAJOR HISTOCOMPATIBILITY GENE [J].
BALDWIN, AS ;
SHARP, PA .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (01) :305-313
[4]   THE V-REL ONCOGENE ENCODES A KAPPA-B ENHANCER BINDING-PROTEIN THAT INHIBITS NF-KAPPA-B FUNCTION [J].
BALLARD, DW ;
WALKER, WH ;
DOERRE, S ;
SISTA, P ;
MOLITOR, JA ;
DIXON, EP ;
PEFFER, NJ ;
HANNINK, M ;
GREENE, WC .
CELL, 1990, 63 (04) :803-814
[5]   MAX - A HELIX-LOOP-HELIX ZIPPER PROTEIN THAT FORMS A SEQUENCE-SPECIFIC DNA-BINDING COMPLEX WITH MYC [J].
BLACKWOOD, EM ;
EISENMAN, RN .
SCIENCE, 1991, 251 (4998) :1211-1217
[6]   THE SAME INDUCIBLE NUCLEAR PROTEINS REGULATES MITOGEN ACTIVATION OF BOTH THE INTERLEUKIN-2 RECEPTOR-ALPHA GENE AND TYPE-1 HIV [J].
BOHNLEIN, E ;
LOWENTHAL, JW ;
SIEKEVITZ, M ;
BALLARD, DW ;
FRANZA, BR ;
GREENE, WC .
CELL, 1988, 53 (05) :827-836
[7]   THE ONCOPROTEIN BCL-3 DIRECTLY TRANSACTIVATES THROUGH KAPPA-B MOTIFS VIA ASSOCIATION WITH DNA-BINDING P50B HOMODIMERS [J].
BOURS, V ;
FRANZOSO, G ;
AZARENKO, V ;
PARK, S ;
KANNO, T ;
BROWN, K ;
SIEBENLIST, U .
CELL, 1993, 72 (05) :729-739
[8]   AN ENHANCER LOCATED IN A CPG-ISLAND 3' TO THE TCR/CD3-EPSILON GENE CONFERS LYMPHOCYTE-T-SPECIFICITY TO ITS PROMOTER [J].
CLEVERS, H ;
LONBERG, N ;
DUNLAP, S ;
LACY, E ;
TERHORST, C .
EMBO JOURNAL, 1989, 8 (09) :2527-2535
[9]   TRANSCRIPTION FACTORS IN EARLY T-CELL DEVELOPMENT [J].
CLEVERS, HC ;
OOSTERWEGEL, MA ;
GEORGOPOULOS, K .
IMMUNOLOGY TODAY, 1993, 14 (12) :591-596
[10]   4 OF THE 7 ZINC FINGERS OF THE EVI-1 MYELOID-TRANSFORMING GENE ARE REQUIRED FOR SEQUENCE-SPECIFIC BINDING TO GA(C/T)AAGA(T/C)AAGATAA [J].
DELWEL, R ;
FUNABIKI, T ;
KREIDER, BL ;
MORISHITA, K ;
IHLE, JN .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (07) :4291-4300