THE SUA8 SUPPRESSORS OF SACCHAROMYCES-CEREVISIAE ENCODE REPLACEMENTS OF CONSERVED RESIDUES WITHIN THE LARGEST SUBUNIT OF RNA POLYMERASE-II AND AFFECT TRANSCRIPTION START SITE SELECTION SIMILARLY TO SUA7 (TFIIB) MUTATIONS

被引:75
作者
BERROTERAN, RW [1 ]
WARE, DE [1 ]
HAMPSEY, M [1 ]
机构
[1] LOUISIANA STATE UNIV, MED CTR, DEPT BIOCHEM & MOLEC BIOL, 1501 KINGS HIGHWAY, SHREVEPORT, LA 71130 USA
关键词
D O I
10.1128/MCB.14.1.226
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
Mutations in the Saccharomyces cerevisiae sua8 gene were found to be suppressors of an aberrant ATG translation initiation codon in the leader region of the cyc1 gene. Analysis of cyc1 transcripts from sua8 mutants revealed that suppression is a consequence of diminished transcription initiation at the normal start sites in favor of initiation at downstream sites, including a site between the aberrant and normal ATG start codons. This effect is not cyc1 gene specific since initiation at other genes, including ADH1, CYC7, and HIS4, was similarly affected, although initiation at HIS3 and SPT15 was unaffected. The SUA8 gene was cloned and partially sequenced, revealing identity to RPB1, which encodes the largest subunit of RNA polymerase II. The sua8 suppressors are the result of single amino acid replacements of highly conserved residues. Three replacements were found either within or immediately preceding homology block D, and a fourth was found adjacent to homology block H, indicating that these regions play a role in defining start sites in vivo. Nearly identical effects on start site selection were observed for sua7 suppressors, which encode altered forms of TFIIB. Synthetic lethality was associated with double sua7 sua8 suppressor mutations, and recessive sua7 mutants failed to fully complement recessive sua8 mutants in heterozygous diploids (nonallelic noncomplementation). These data indicate that the largest subunit of RNA polymerase II and TFIIB are important determinants of transcription start site selection in S. cerevisiae and suggest that this function might be conferred by interaction between these two proteins.
引用
收藏
页码:226 / 237
页数:12
相关论文
共 92 条
[1]  
AHEARN JM, 1987, J BIOL CHEM, V262, P10695
[2]   EXTENSIVE HOMOLOGY AMONG THE LARGEST SUBUNITS OF EUKARYOTIC AND PROKARYOTIC RNA-POLYMERASES [J].
ALLISON, LA ;
MOYLE, M ;
SHALES, M ;
INGLES, CJ .
CELL, 1985, 42 (02) :599-610
[3]   A SUPPRESSOR OF A HIS4 TRANSCRIPTIONAL DEFECT ENCODES A PROTEIN WITH HOMOLOGY TO THE CATALYTIC SUBUNIT OF PROTEIN PHOSPHATASES [J].
ARNDT, KT ;
STYLES, CA ;
FINK, GR .
CELL, 1989, 56 (04) :527-537
[4]   SIMIAN VIRUS-40 MAJOR LATE PROMOTER - A NOVEL TRIPARTITE STRUCTURE THAT INCLUDES INTRAGENIC SEQUENCES [J].
AYER, DE ;
DYNAN, WS .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2021-2033
[5]   DELINEATION OF 2 FUNCTIONAL REGIONS OF TRANSCRIPTION FACTOR-TFIIB [J].
BARBERIS, A ;
MULLER, CW ;
HARRISON, SC ;
PTASHNE, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (12) :5628-5632
[6]   INITIATION OF TRANSCRIPTION OF THE ERYTHROID PROMOTER OF THE PORPHOBILINOGEN DEAMINASE GENE IS REGULATED BY A CIS-ACTING SEQUENCE AROUND THE CAP SITE [J].
BEAUPAIN, D ;
ELEOUET, JF ;
ROMEO, PH .
NUCLEIC ACIDS RESEARCH, 1990, 18 (22) :6509-6515
[7]  
BENNETZEN JL, 1982, J BIOL CHEM, V257, P3018
[8]   INVIVO SEQUENCE REQUIREMENTS OF THE SV40 EARLY PROMOTER REGION [J].
BENOIST, C ;
CHAMBON, P .
NATURE, 1981, 290 (5804) :304-310
[9]   RELATEDNESS OF ARCHAEBACTERIAL RNA-POLYMERASE CORE SUBUNITS TO THEIR EUBACTERIAL AND EUKARYOTIC EQUIVALENTS [J].
BERGHOFER, B ;
KROCKEL, L ;
KORTNER, C ;
TRUSS, M ;
SCHALLENBERG, J ;
KLEIN, A .
NUCLEIC ACIDS RESEARCH, 1988, 16 (16) :8113-8128
[10]   NF-KAPPA-B-MEDIATED ACTIVATION OF THE HUMAN IMMUNODEFICIENCY VIRUS ENHANCER - SITE OF TRANSCRIPTIONAL INITIATION IS INDEPENDENT OF THE TATA BOX [J].
BIELINSKA, A ;
KRASNOW, S ;
NABEL, GJ .
JOURNAL OF VIROLOGY, 1989, 63 (09) :4097-4100