The features of Drosophila core promoters revealed by statistical analysis

被引:38
作者
Gershenzon, Naum I.
Trifonov, Edward N.
Ioshikhes, Ilya P.
机构
[1] Ohio State Univ, Dept Biomed Informat, Columbus, OH 43210 USA
[2] Wright State Univ, Dept Phys, Dayton, OH 45435 USA
[3] Univ Haifa, Genome Divers Ctr, Inst Evolut, IL-31905 Haifa, Israel
关键词
D O I
10.1186/1471-2164-7-161
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Experimental investigation of transcription is still a very labor- and time-consuming process. Only a few transcription initiation scenarios have been studied in detail. The mechanism of interaction between basal machinery and promoter, in particular core promoter elements, is not known for the majority of identified promoters. In this study, we reveal various transcription initiation mechanisms by statistical analysis of 3393 nonredundant Drosophila promoters. Results: Using Drosophila-specific position-weight matrices, we identified promoters containing TATA box, Initiator, Downstream Promoter Element (DPE), and Motif Ten Element (MTE), as well as core elements discovered in Human ( TFIIB Recognition Element (BRE) and Downstream Core Element (DCE)). Promoters utilizing known synergetic combinations of two core elements (TATA_Inr, Inr_MTE, Inr_DPE, and DPE_MTE) were identified. We also establish the existence of promoters with potentially novel synergetic combinations: TATA_DPE and TATA_MTE. Our analysis revealed several motifs with the features of promoter elements, including possible novel core promoter element(s). Comparison of Human and Drosophila showed consistent percentages of promoters with TATA, Inr, DPE, and synergetic combinations thereof, as well as most of the same functional and mutual positions of the core elements. No statistical evidence of MTE utilization in Human was found. Distinct nucleosome positioning in particular promoter classes was revealed. Conclusion: We present lists of promoters that potentially utilize the aforementioned elements/combinations. The number of these promoters is two orders of magnitude larger than the number of promoters in which transcription initiation was experimentally studied. The sequences are ready to be experimentally tested or used for further statistical analysis. The developed approach may be utilized for other species.
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页数:13
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共 49 条
[1]   Chromatin structure and the regulation of gene expression: Remodeling at the MMTV promoter [J].
Beato, M .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1996, 74 (12) :711-724
[2]   Interaction of steroid hormone receptors with transcription factors involves chromatin remodelling [J].
Beato, M ;
Candau, R ;
Chavez, S ;
Mows, C ;
Truss, M .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1996, 56 (1-6) :47-59
[3]   Transcriptional regulation in Drosophila: The post-genome challenge [J].
Biggin M.D. ;
Tjian R. .
Functional & Integrative Genomics, 2001, 1 (4) :223-234
[4]  
Bolshoy A, 1996, COMPUT APPL BIOSCI, V12, P383
[5]   WEIGHT MATRIX DESCRIPTIONS OF 4 EUKARYOTIC RNA POLYMERASE-II PROMOTER ELEMENTS DERIVED FROM 502 UNRELATED PROMOTER SEQUENCES [J].
BUCHER, P .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 212 (04) :563-578
[6]   The downstream core promoter element, DPE, is conserved from Drosophila to humans and is recognized by TAF(II)60 of Drosophila [J].
Burke, TW ;
Kadonaga, JT .
GENES & DEVELOPMENT, 1997, 11 (22) :3020-3031
[7]   Biochemistry and structural biology of transcription factor IID (TFIID) [J].
Burley, SK ;
Roeder, RG .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :769-799
[8]   Nucleosome-mediated synergism between transcription factors on the mouse mammary tumor virus promoter [J].
Chavez, S ;
Beato, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) :2885-2890
[9]   Mechanism of synergy between TATA and initiator: synergistic binding of TFIID following a putative TFIIA-induced isomerization [J].
Emami, KH ;
Jain, A ;
Smale, ST .
GENES & DEVELOPMENT, 1997, 11 (22) :3007-3019
[10]   Chromatin organization and transcriptional control of gene expression in Drosophila [J].
Farkas, G ;
Leibovitch, BA ;
Elgin, SCR .
GENE, 2000, 253 (02) :117-136