Widespread selection for local RNA secondary structure in coding regions of bacterial genes

被引:157
作者
Katz, L [1 ]
Burge, CB [1 ]
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
D O I
10.1101/gr.1257503
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
Redundancy of the genetic code dictates that a given protein can be encoded by a large collection of distinct mRNA species, potentially allowing mRNAs to simultaneously optimize desirable RNA structural features in addition to their protein-coding function. To determine whether natural mRNAs exhibit biases related to local RNA secondary structure, a new randomization procedure was developed, DicodonShuffle, which randomizes mRNA sequences while preserving the same encoded protein sequence, the same codon usage, and the same dinucleotide composition as the native message. Genes from 10 of 14 eubacterial species studied and one eukaryote, the yeast Saccharomyces cerevisiae, exhibited statistically significant biases in favor of local RNA structure as measured by folding free energy. Several significant associations Suggest functional roles for mRNA structure, including stronger secondary structure bias in the coding regions of intron-containing yeast genes than in intronless genes, and significantly higher folding potential in polycistronic messages than in monocistronic messages in Escherichia coli. Potential secondary structure generally increased in genes from the 5' to the 3' end of E coli operons, and secondary structure potential was conserved in homologous Salmonella typhi operons. These results are interpreted in terms of possible roles of RNA structures in RNA processing, regulation of mRNA stability, and translational control.
引用
收藏
页码:2042 / 2051
页数:10
相关论文
共 43 条
[1]   The ins and outs of group II introns [J].
Bonen, L ;
Vogel, J .
TRENDS IN GENETICS, 2001, 17 (06) :322-331
[2]   Transcript analysis of 1003 novel yeast genes using high-throughput northern hybridizations [J].
Brown, AJP ;
Planta, RJ ;
Restuhadi, F ;
Bailey, DA ;
Butler, PR ;
Cadahia, JL ;
Cerdan, ME ;
De Jonge, M ;
Gardner, DCJ ;
Gent, ME ;
Hayes, A ;
Kolen, CPAM ;
Lombardia, LJ ;
Murad, AMA ;
Oliver, RA ;
Sefton, M ;
Thevelein, JM ;
Tournu, H ;
van Delft, YJ ;
Verbart, DJ ;
Winderickx, J ;
Oliver, SG .
EMBO JOURNAL, 2001, 20 (12) :3177-3186
[3]   Genome signature comparisons among prokaryote, plasmid, and mitochondrial DNA [J].
Campbell, A ;
Mrázek, J ;
Karlin, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) :9184-9189
[4]   Controlling messenger RNA stability in bacteria: Strategies for engineering gene expression [J].
Carrier, TA ;
Keasling, JD .
BIOTECHNOLOGY PROGRESS, 1997, 13 (06) :699-708
[5]   Structural elements required for the localization of ASH1 mRNA and of a green fluorescent protein reporter particle in vivo [J].
Chartrand, P ;
Meng, XH ;
Singer, RH ;
Long, RM .
CURRENT BIOLOGY, 1999, 9 (06) :333-336
[6]  
Deutscher MP, 2001, PROG NUCLEIC ACID RE, V66, P67
[7]  
Diwa A, 2000, GENE DEV, V14, P1249
[8]   Predictive identification of exonic splicing enhancers in human genes [J].
Fairbrother, WG ;
Yeh, RF ;
Sharp, PA ;
Burge, CB .
SCIENCE, 2002, 297 (5583) :1007-1013
[9]   AUTOGENOUS CONTROL OF THE S10 RIBOSOMAL-PROTEIN OPERON OF ESCHERICHIA-COLI - GENETIC DISSECTION OF TRANSCRIPTIONAL AND POSTTRANSCRIPTIONAL REGULATION [J].
FREEDMAN, LP ;
ZENGEL, JM ;
ARCHER, RH ;
LINDAHL, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (18) :6516-6520
[10]   EVIDENCE FOR SYMBIOTIC ORIGIN OF MITOCHONDRIA [J].
FRIDOVICH, I .
LIFE SCIENCES, 1974, 14 (05) :819-826