TRANSLATIONAL CONTROL IN PRODUCTION OF TRANSPOSASE AND IN TRANSPOSITION OF INSERTION SEQUENCE-IS3

被引:124
作者
SEKINE, Y [1 ]
EISAKI, N [1 ]
OHTSUBO, E [1 ]
机构
[1] UNIV TOKYO, INST MOLEC & CELLULAR BIOSCI, YAYOI 1-1-1, BUNKYO KU, TOKYO 113, JAPAN
关键词
MINICIRCLES; MINIPLASMIDS; PSEUDOKNOT; TRANSLATIONAL COUPLING; TRANSLATIONAL FRAMESHIFTING;
D O I
10.1006/jmbi.1994.1097
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
IS3 (1258 bp in length) contains two open reading frames orfA and orfB, which are out of phase and overlap each other. We show here that three proteins of 10, 32 and 42 kDa in size are encoded by IS3. The 10 kDa protein is the product of orfA and is here called OrfA. The ATG codon of orfB which overlaps the termination codon of orfA is utilized to produce the 32 kDa protein (here called OrfB), in a manner depending on translation of orfA. The 42 kDa protein is a transframe protein (here called OrfB), which is synthesized from orfA and orfB by -1 translational frameshifting at the A4G motif present in the overlapping region. Both the frameshifting event to produce OrfB and the coupled translation event to produce OrfB are greatly stimulated by a pseudo knot structure located in the overlapping region between orfA and orfB. A mutant IS3 with a single base insertion in the A4G motif efficiently produces the OrfB transframe protein without frameshifting. This mutant was found not to mediate co-integration but to mediate adjacent deletion to produce various miniplasmids and minicircles in large amounts. The OrfB transframe protein is necessary and sufficient for formation of these deletion products, implying that it is the transposase. Most of the minicircles consisted solely of the entire IS3 sequence and a three base-pair sequence between the IS3 ends. The significance of minicircle formation is discussed. © 1994 Academic Press Limited.
引用
收藏
页码:1406 / 1420
页数:15
相关论文
共 58 条
[51]  
VARMUS H, 1989, MOBILE DNA, P55
[52]  
VIEIRA J, 1987, METHOD ENZYMOL, V153, P3
[53]   HIGH-LEVEL RIBOSOMAL FRAMESHIFTING DIRECTS THE SYNTHESIS OF IS150 GENE-PRODUCTS [J].
VOGELE, K ;
SCHWARTZ, E ;
WELZ, C ;
SCHILTZ, E ;
RAK, B .
NUCLEIC ACIDS RESEARCH, 1991, 19 (16) :4377-4385
[54]   CONSTRUCTION AND CHARACTERIZATION OF THE DELETION MUTANT OF HUPA AND HUPB GENES IN ESCHERICHIA-COLI [J].
WADA, M ;
KANO, Y ;
OGAWA, T ;
OKAZAKI, T ;
IMAMOTO, F .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 204 (03) :581-591
[55]  
Watson R J, 1991, DNA Seq, V2, P163, DOI 10.3109/10425179109039686
[56]   IMPROVED M13 PHAGE CLONING VECTORS AND HOST STRAINS - NUCLEOTIDE-SEQUENCES OF THE M13MP18 AND PUC19 VECTORS [J].
YANISCHPERRON, C ;
VIEIRA, J ;
MESSING, J .
GENE, 1985, 33 (01) :103-119
[57]   REPRESSOR GENE FINO IN PLASMIDS R100 AND PLASMID-F - CONSTITUTIVE TRANSFER OF PLASMID-F IS CAUSED BY INSERTION OF IS3 INTO F-FINO [J].
YOSHIOKA, Y ;
OHTSUBO, H ;
OHTSUBO, E .
JOURNAL OF BACTERIOLOGY, 1987, 169 (02) :619-623
[58]   THE REGULATORY ROLE OF THE IS 1-ENCODED INSA PROTEIN IN TRANSPOSITION [J].
ZERBIB, D ;
POLARD, P ;
ESCOUBAS, JM ;
GALAS, D ;
CHANDLER, M .
MOLECULAR MICROBIOLOGY, 1990, 4 (03) :471-477