Correlations between Shine-Dalgarno sequences and gene features such as predicted expression levels and operon structures

被引:239
作者
Ma, J
Campbell, A
Karlin, S [1 ]
机构
[1] Stanford Univ, Dept Math, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Sci Biol, Stanford, CA 94305 USA
关键词
D O I
10.1128/JB.184.20.5733-5745.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This work assesses relationships for 30 complete prokaryotic genomes between the presence of the Shine-Dalgarno (SD) sequence and other gene features, including expression levels, type of start codon, and distance between successive genes. A significant positive correlation of the presence of an SD sequence and the predicted expression level of a gene based on codon usage biases was ascertained, such that predicted highly expressed genes are more likely to possess a strong SD sequence than average genes. Genes with AUG start codons are more likely than genes with other start codons, GUG or UUG, to possess an SD sequence. Genes in close proximity to upstream genes on the same coding strand in most genomes are significantly higher in SD presence. In light of these results, we discuss the role of the SD sequence in translation initiation and its relationship with predicted gene expression levels and with operon structure in both bacterial and archaeal genomes.
引用
收藏
页码:5733 / 5745
页数:13
相关论文
共 59 条
[1]   First steps from a two-dimensional protein index towards a response-regulation map for Bacillus subtilis [J].
Antelmann, H ;
Bernhardt, J ;
Schmid, R ;
Mach, H ;
Volker, U ;
Hecker, M .
ELECTROPHORESIS, 1997, 18 (08) :1451-1463
[2]   The complete atomic structure of the large ribosomal subunit at 2.4 Å resolution [J].
Ban, N ;
Nissen, P ;
Hansen, J ;
Moore, PB ;
Steitz, TA .
SCIENCE, 2000, 289 (5481) :905-920
[3]   GeneMarkS: a self-training method for prediction of gene starts in microbial genomes. Implications for finding sequence motifs in regulatory regions [J].
Besemer, J ;
Lomsadze, A ;
Borodovsky, M .
NUCLEIC ACIDS RESEARCH, 2001, 29 (12) :2607-2618
[4]   The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[5]   The structural basis for the action of the antibiotics tetracycline, pactamycin, and hygromycin B on the 30S ribosomal subunit [J].
Brodersen, DE ;
Clemons, WM ;
Carter, AP ;
Morgan-Warren, RJ ;
Wimberly, BT ;
Ramakrishnan, V .
CELL, 2000, 103 (07) :1143-1154
[6]   Functional insights from the structure of the 30S ribosomal subunit and its interactions with antibiotics [J].
Carter, AP ;
Clemons, WM ;
Brodersen, DE ;
Morgan-Warren, RJ ;
Wimberly, BT ;
Ramakrishnan, V .
NATURE, 2000, 407 (6802) :340-348
[7]   DETERMINATION OF THE OPTIMAL ALIGNED SPACING BETWEEN THE SHINE-DALGARNO SEQUENCE AND THE TRANSLATION INITIATION CODON OF ESCHERICHIA-COLI MESSENGER-RNAS [J].
CHEN, HY ;
BJERKNES, M ;
KUMAR, R ;
JAY, E .
NUCLEIC ACIDS RESEARCH, 1994, 22 (23) :4953-4957
[8]   Cis-acting signals controlling translational initiation in the thermophilic archaeon Sulfolobus solfataricus [J].
Condò, I ;
Ciammaruconi, A ;
Benelli, D ;
Ruggero, D ;
Londei, P .
MOLECULAR MICROBIOLOGY, 1999, 34 (02) :377-384
[9]   TRANSLATIONAL INITIATION ON STRUCTURED MESSENGERS - ANOTHER ROLE FOR THE SHINE-DALGARNO INTERACTION [J].
DESMIT, MH ;
VANDUIN, J .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 235 (01) :173-184
[10]  
DESMIT MH, 1993, MOL MICROBIOL, V9, P1079