Spt10-dependent transcriptional activation in Saccharomyces cerevisiae requires both the Spt10 acetyltransferase domain and Spt21

被引:32
作者
Hess, D
Liu, BS
Roan, NR
Sternglanz, R
Winston, F
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[2] SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
关键词
D O I
10.1128/MCB.24.1.135-143.2004
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
Histone levels are a key factor in several nuclear processes, including transcription and chromosome segregation. Previous studies have demonstrated that Spt10 and Spt21 are required for the normal transcription of a subset of the histone genes in Saccharomyces cerevisiae, and sequence analysis has suggested that Spt10 is an acetyltransferase. We have now characterized several aspects of transcriptional activation of histone genes by Spt10 in vivo. Our results show that activation by Spt10 is dependent on its acetyltransferase domain. At HTA2-HTB2, the histone locus whose transcription is most strongly dependent on Spt10, Spt10 is physically recruited to the promoter in an Spt21-dependent and a cell cycle-dependent manner. Furthermore, Spt10 and Spt21 directly interact. These results, taken together with the identification of spt10 mutations that suppress an spt21Delta mutation, suggest a model for transcriptional activation by Spt10 and Spt21.
引用
收藏
页码:135 / 143
页数:9
相关论文
共 40 条
[1]  
Ausubel F.M., 1988, CURRENT PROTOCOLS MO
[2]   A SIMPLE AND EFFICIENT METHOD FOR DIRECT GENE DELETION IN SACCHAROMYCES-CEREVISIAE [J].
BAUDIN, A ;
OZIERKALOGEROPOULOS, O ;
DENOUEL, A ;
LACROUTE, F ;
CULLIN, C .
NUCLEIC ACIDS RESEARCH, 1993, 21 (14) :3329-3330
[3]   A POSITIVE SELECTION FOR MUTANTS LACKING OROTIDINE-5'-PHOSPHATE DECARBOXYLASE ACTIVITY IN YEAST - 5-FLUORO-OROTIC ACID RESISTANCE [J].
BOEKE, JD ;
LACROUTE, F ;
FINK, GR .
MOLECULAR & GENERAL GENETICS, 1984, 197 (02) :345-346
[4]  
Burke D., 2000, Methods in Yeast Genetics Plainview, NY, V2000
[5]   A genome-wide transcriptional analysis of the mitotic cell cycle [J].
Cho, RJ ;
Campbell, MJ ;
Winzeler, EA ;
Steinmetz, L ;
Conway, A ;
Wodicka, L ;
Wolfsberg, TG ;
Gabrielian, AE ;
Landsman, D ;
Lockhart, DJ ;
Davis, RW .
MOLECULAR CELL, 1998, 2 (01) :65-73
[6]   Finding functional features in Saccharomyces genomes by phylogenetic footprinting [J].
Cliften, P ;
Sudarsanam, P ;
Desikan, A ;
Fulton, L ;
Fulton, B ;
Majors, J ;
Waterston, R ;
Cohen, BA ;
Johnston, M .
SCIENCE, 2003, 301 (5629) :71-76
[7]  
DENIS CL, 1990, GENETICS, V124, P283
[8]   SPT10 AND SPT21 ARE REQUIRED FOR TRANSCRIPTION OF PARTICULAR HISTONE GENES IN SACCHAROMYCES-CEREVISIAE [J].
DOLLARD, C ;
RICUPEROHOVASSE, SL ;
NATSOULIS, G ;
BOEKE, JD ;
WINSTON, F .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (08) :5223-5228
[9]   ISOLATION OF YEAST HISTONE GENES H2A AND H2B [J].
HEREFORD, L ;
FAHRNER, K ;
WOOLFORD, J ;
ROSBASH, M ;
KABACK, DB .
CELL, 1979, 18 (04) :1261-1271
[10]   Genomic binding sites of the yeast cell-cycle transcription factors SBF and MBF [J].
Iyer, VR ;
Horak, CE ;
Scafe, CS ;
Botstein, D ;
Snyder, M ;
Brown, PO .
NATURE, 2001, 409 (6819) :533-538