SYNTHESIS OF STAPHYLOCOCCAL VIRULENCE FACTORS IS CONTROLLED BY A REGULATORY RNA MOLECULE

被引:825
作者
NOVICK, RP
ROSS, HF
PROJAN, SJ
KORNBLUM, J
KREISWIRTH, B
MOGHAZEH, S
机构
[1] Department of Plasmid Biology, Public Health Research Institute, New York, NY 10016
关键词
AGR LOCUS; STAPHYLOCOCCUS-AUREUS; TRANSCRIPTION REGULATION; TRANSLATION REGULATION;
D O I
10.1002/j.1460-2075.1993.tb06074.x
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
The production of most toxins and other exoproteins in Staphylococcus aureus is controlled globally by a complex polycistronic regulatory locus, agr. Secretory proteins are up-regulated by agr whereas surface proteins are down-regulated. agr contains two divergent promoters, one of which directs the synthesis of a 514 nucleotide (nt) transcript, RNAIII. In this report, we show that the cloned RNAIII determinant restores both positive and negative regulatory functions of agr to an agr-null strain and that the RNA itself, rather than any protein, is the effector molecule. RNAIII acts primarily on the initiation of transcription and, secondarily in some cases, at the level of translation. In these cases, translation and transcription are regulated independently. RNAIII probably regulates translation directly by interacting with target gene transcripts and transcription indirectly by means of intermediary protein factors.
引用
收藏
页码:3967 / 3975
页数:9
相关论文
共 52 条
[1]  
ARVIDSON S, 1989, GENETIC TRANSFORMATI, P511
[2]   SIZING AND MAPPING OF EARLY ADENOVIRUS MESSENGER-RNAS BY GEL-ELECTROPHORESIS OF S1 ENDONUCLEASE-DIGESTED HYBRIDS [J].
BERK, AJ ;
SHARP, PA .
CELL, 1977, 12 (03) :721-732
[3]   A RAPID, SENSITIVE METHOD FOR DETECTION OF ALKALINE-PHOSPHATASE CONJUGATED ANTI-ANTIBODY ON WESTERN BLOTS [J].
BLAKE, MS ;
JOHNSTON, KH ;
RUSSELLJONES, GJ ;
GOTSCHLICH, EC .
ANALYTICAL BIOCHEMISTRY, 1984, 136 (01) :175-179
[4]   HIGH-FREQUENCY TRANSFORMATION OF BACILLUS-SUBTILIS PROTOPLASTS BY PLASMID DNA [J].
CHANG, S ;
COHEN, SN .
MOLECULAR & GENERAL GENETICS, 1979, 168 (01) :111-115
[5]   REGULATION OF EXOPROTEIN EXPRESSION IN STAPHYLOCOCCUS-AUREUS BY A LOCUS (SAR) DISTINCT FROM AGR [J].
CHEUNG, AL ;
KOOMEY, JM ;
BUTLER, CA ;
PROJAN, SJ ;
FISCHETTI, VA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6462-6466
[6]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[7]   CLONING AND EXPRESSION IN ESCHERICHIA-COLI AND STAPHYLOCOCCUS-AUREUS OF THE BETA-LYSIN DETERMINANT FROM STAPHYLOCOCCUS-AUREUS - EVIDENCE THAT BACTERIOPHAGE CONVERSION OF BETA-LYSIN ACTIVITY IS CAUSED BY INSERTIONAL INACTIVATION OF THE BETA-LYSIN DETERMINANT [J].
COLEMAN, DC ;
ARBUTHNOTT, JP ;
POMEROY, HM ;
BIRKBECK, TH .
MICROBIAL PATHOGENESIS, 1986, 1 (06) :549-564
[8]   PRIMARY SEQUENCE OF THE ALPHA-TOXIN GENE FROM STAPHYLOCOCCUS-AUREUS WOOD-46 [J].
GRAY, GS ;
KEHOE, M .
INFECTION AND IMMUNITY, 1984, 46 (02) :615-618
[9]   NUCLEOTIDE-SEQUENCE AND FUNCTIONAL MAP OF PE194, A PLASMID THAT SPECIFIES INDUCIBLE RESISTANCE TO MACROLIDE, LINCOSAMIDE, AND STREPTOGRAMIN TYPE-B ANTIBIOTICS [J].
HORINOUCHI, S ;
WEISBLUM, B .
JOURNAL OF BACTERIOLOGY, 1982, 150 (02) :804-814
[10]  
JANZON L, 1986, FEMS MICROBIOL LETT, V33, P193