IDENTICAL COMPONENTS OF YEAST TRANSCRIPTION FACTOR-IIIB ARE REQUIRED AND SUFFICIENT FOR TRANSCRIPTION OF TATA BOX-CONTAINING AND TATA-LESS GENES

被引:75
作者
JOAZEIRO, CAP
KASSAVETIS, GA
GEIDUSCHEK, EP
机构
[1] UNIV CALIF SAN DIEGO,CTR MOLEC GENET,9500 GILMAN DR,LA JOLLA,CA 92093
[2] UNIV CALIF SAN DIEGO,DEPT BIOL,LA JOLLA,CA 92093
关键词
D O I
10.1128/MCB.14.4.2798
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
Specific transcription by RNA polymerase III requires recognition of the promoter-bound transcription factor IIIB (TFIIIB), of which the TATA-binding protein (TBP) is a subunit. The recruitment of TFIIIB to TATA-less genes is mediated by protein-protein interactions with transcription factor IIIC (TFIIIC) bound to the box A and box B elements. Here we examine interactions involved in the recruitment of TFIIIB to the TATA element-containing yeast U6 small nuclear RNA gene SNR6. TFIIIC is not required for the formation of TFIIIB-SNR6 gene complexes with purified components. The same three components of TFIIIB that are necessary for TFIIIC-dependent transcription of tRNA genes (recombinant TBP and Brf and the denaturing-gel-purified 90-kDa subunit) are required and sufficient for TATA box-directed U6 transcription. Despite its TFIIIC-independent, DNA sequence-dependent assembly, the TFIIIB-SNR6 complex shares important features with tDNA- and 5S rDNA-TFIIIB complexes, such as extent and location of footprint, stability, and resistance to heparin. These properties are clearly distinct from those of a TBP-SNR6 complex. In the SNR6 gene, box B, the primary binding site for TFIIIC, is suboptimally spaced relative to box A. At limiting TBP concentrations and on bare DNA, TFIIIC stimulates the formation of TFIIIB complexes with SNR6 but contributes poorly, at best, to the formation of properly placed complexes.
引用
收藏
页码:2798 / 2808
页数:11
相关论文
共 35 条
[1]  
BAKER RE, 1986, J BIOL CHEM, V261, P5275
[2]   MULTIPLE STATES OF PROTEIN DNA INTERACTION IN THE ASSEMBLY OF TRANSCRIPTION COMPLEXES ON SACCHAROMYCES-CEREVISIAE 5S RIBOSOMAL-RNA GENES [J].
BRAUN, BR ;
RIGGS, DL ;
KASSAVETIS, GA ;
GEIDUSCHEK, EP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (08) :2530-2534
[3]  
BRAUN BR, 1992, J BIOL CHEM, V267, P22562
[4]   SPLICEOSOMAL RNA U6 IS REMARKABLY CONSERVED FROM YEAST TO MAMMALS [J].
BROW, DA ;
GUTHRIE, C .
NATURE, 1988, 334 (6179) :213-218
[5]   TRANSCRIPTION OF A YEAST U6 SNRNA GENE REQUIRES A POLYMERASE-III PROMOTER ELEMENT IN A NOVEL POSITION [J].
BROW, DA ;
GUTHRIE, C .
GENES & DEVELOPMENT, 1990, 4 (08) :1345-1356
[6]   PROCEDURE FOR RAPID, LARGE-SCALE PURIFICATION OF ESCHERICHIA-COLI DNA-DEPENDENT RNA-POLYMERASE INVOLVING POLYMIN-P PRECIPITATION AND DNA-CELLULOSE CHROMATOGRAPHY [J].
BURGESS, RR ;
JENDRISAK, JJ .
BIOCHEMISTRY, 1975, 14 (21) :4634-4638
[7]   TFIIIC RELIEVES REPRESSION OF U6 SNRNA TRANSCRIPTION BY CHROMATIN [J].
BURNOL, AF ;
MARGOTTIN, F ;
HUET, J ;
ALMOUZNI, G ;
PRIOLEAU, MN ;
MECHALI, M ;
SENTENAC, A .
NATURE, 1993, 362 (6419) :475-477
[8]  
COLBERT T, 1992, GENE DEV, V6, P1949
[9]  
CROTHERS DM, 1991, METHOD ENZYMOL, V208, P118
[10]  
DIECI G, 1993, J BIOL CHEM, V268, P11199