Comprehensive analysis of transcriptional promoter structure and function in 1% of the human genome

被引:193
作者
Cooper, SJ [1 ]
Trinklein, ND [1 ]
Anton, ED [1 ]
Nguyen, L [1 ]
Myers, RM [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
关键词
D O I
10.1101/gr.4222606
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
Transcriptional promoters comprise one of many classes Of eukaryotic transcriptional regulatory elements. Identification and characterization of these elements are vital to Understanding the complex network of human gene regulation. using full-length cDNA sequences to identify transcription start sites (TSS), we predicted more than 900 putative human transcriptional promoters in the ENCODE regions, representing a comprehensive sampling of promoters in 1% of the genome. We identified 387 fragments that function as promoters in at least one of 16 cell lines by measuring promoter activity ill high-throughput transient transfection reporter assays. These positive functional results demonstrate widespread use of alternative promoters. We show a strong correlation between promoter activity and the corresponding endogenous RNA transcript levels, providing the first experimental quantitative estimate of promoter contribution to gene regulation. Finally, we identified functional regions within a randomly selected subset of 45 promoters Using deletion analyses. These experiments showed that, oil average, the sequence -300 to -50 bp of the TSS positively contributes to core promoter activity. Interestingly, putative negative elements were identified -1000 to -500 bp upstream of the TSS for 55% of genes tested. These data provide the largest and most comprehensive view of promoter function in the human genome.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 43 条
[1]   Exploiting human-fish genome comparisons for deciphering gene regulation [J].
Ahituv, N ;
Rubin, EM ;
Nobrega, MA .
HUMAN MOLECULAR GENETICS, 2004, 13 :R261-R266
[2]  
[Anonymous], 2003, Applied Soft Computing, DOI DOI 10.1016/J.AS0C.2003.05.001
[3]  
Bailey T., 1994, P 2 INT C INT SYST M, P28
[4]   Global identification of human transcribed sequences with genome tiling arrays [J].
Bertone, P ;
Stolc, V ;
Royce, TE ;
Rozowsky, JS ;
Urban, AE ;
Zhu, XW ;
Rinn, JL ;
Tongprasit, W ;
Samanta, M ;
Weissman, S ;
Gerstein, M ;
Snyder, M .
SCIENCE, 2004, 306 (5705) :2242-2246
[5]   Hitting their targets: an emerging picture of E2F and cell cycle control [J].
Blais, A ;
Dynlacht, BD .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2004, 14 (05) :527-532
[6]   LAGAN and Multi-LAGAN: Efficient tools for large-scale multiple alignment of genomic DNA [J].
Brudno, M ;
Do, CB ;
Cooper, GM ;
Kim, MF ;
Davydov, E ;
Green, ED ;
Sidow, A ;
Batzoglou, S .
GENOME RESEARCH, 2003, 13 (04) :721-731
[7]   The RNA polymerase II core promoter: a key component in the regulation of gene expression [J].
Butler, JEF ;
Kadonaga, JT .
GENES & DEVELOPMENT, 2002, 16 (20) :2583-2592
[8]   Distribution and intensity of constraint in mammalian genomic sequence [J].
Cooper, GM ;
Stone, EA ;
Asimenos, G ;
Green, ED ;
Batzoglou, S ;
Sidow, A .
GENOME RESEARCH, 2005, 15 (07) :901-913
[9]   ANALYSIS OF EXTREME VALUES [J].
DIXON, WJ .
ANNALS OF MATHEMATICAL STATISTICS, 1950, 21 (04) :488-506
[10]   The ENCODE (ENCyclopedia of DNA elements) Project [J].
Feingold, EA ;
Good, PJ ;
Guyer, MS ;
Kamholz, S ;
Liefer, L ;
Wetterstrand, K ;
Collins, FS ;
Gingeras, TR ;
Kampa, D ;
Sekinger, EA ;
Cheng, J ;
Hirsch, H ;
Ghosh, S ;
Zhu, Z ;
Pate, S ;
Piccolboni, A ;
Yang, A ;
Tammana, H ;
Bekiranov, S ;
Kapranov, P ;
Harrison, R ;
Church, G ;
Struhl, K ;
Ren, B ;
Kim, TH ;
Barrera, LO ;
Qu, C ;
Van Calcar, S ;
Luna, R ;
Glass, CK ;
Rosenfeld, MG ;
Guigo, R ;
Antonarakis, SE ;
Birney, E ;
Brent, M ;
Pachter, L ;
Reymond, A ;
Dermitzakis, ET ;
Dewey, C ;
Keefe, D ;
Denoeud, F ;
Lagarde, J ;
Ashurst, J ;
Hubbard, T ;
Wesselink, JJ ;
Castelo, R ;
Eyras, E ;
Myers, RM ;
Sidow, A ;
Batzoglou, S .
SCIENCE, 2004, 306 (5696) :636-640