TN10 INSERTION SPECIFICITY IS STRONGLY DEPENDENT UPON SEQUENCES IMMEDIATELY ADJACENT TO THE TARGET-SITE CONSENSUS SEQUENCE

被引:70
作者
BENDER, J [1 ]
KLECKNER, N [1 ]
机构
[1] HARVARD UNIV, DEPT BIOCHEM & MOLEC BIOL, CAMBRIDGE, MA 02138 USA
关键词
TRANSPOSON; MUTATIONAL ANALYSIS; DNA-PROTEIN INTERACTIONS;
D O I
10.1073/pnas.89.17.7996
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transposon Tn10 inserts preferentially into particular "hotspots" that have been shown by sequence analysis to contain the symmetrical consensus sequence 5'-GCTNAGC-3'. This consensus is necessary but not sufficient to determine insertion specificity. We have mutagenized a known hotspot to identify other determinants for insertion into this site. This genetic dissection of the sequence context of a protein binding site shows that a second major determinant for Tn10 insertion specificity is contributed by the 6-9 base pairs that flank each end of the consensus sequence. Variations in these context base pairs can confer variations of at least 1000-fold in insertion frequency. There is no discernible consensus sequence for the context determinant, suggesting that sequence-specific protein-DNA contacts are not playing a major role. Taken together with previous work, the observations presented suggest a model for the interaction of transposase with the insertion site: symmetrically disposed subunits bind with specific contacts to the major groove of consensus-sequence base pairs, while flanking sequences influence the interaction through effects on DNA helix structure. We also show that the determinants important for insertion into a site are not important for transposition out of that site.
引用
收藏
页码:7996 / 8000
页数:5
相关论文
共 31 条
[11]   ESCHERICHIA-COLI INTEGRATION HOST FACTOR BINDS SPECIFICALLY TO THE ENDS OF THE INSERTION-SEQUENCE IS1 AND TO ITS MAJOR INSERTION HOT-SPOT IN PBR322 [J].
GAMAS, P ;
CHANDLER, MG ;
PRENTKI, P ;
GALAS, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 195 (02) :261-272
[12]   SEARCHING FOR AND PREDICTING THE ACTIVITY OF SITES FOR DNA-BINDING PROTEINS - COMPILATION AND ANALYSIS OF THE BINDING-SITES FOR ESCHERICHIA-COLI INTEGRATION HOST FACTOR (IHF) [J].
GOODRICH, JA ;
SCHWARTZ, ML ;
MCCLURE, WR .
NUCLEIC ACIDS RESEARCH, 1990, 18 (17) :4993-5000
[13]   DNA-SEQUENCE ORGANIZATION OF IS10-RIGHT OF TN10 AND COMPARISON WITH IS10-LEFT [J].
HALLING, SM ;
SIMONS, RW ;
WAY, JC ;
WALSH, RB ;
KLECKNER, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (08) :2608-2612
[14]   A SYMMETRICAL 6-BASE-PAIR TARGET SITE SEQUENCE DETERMINES TN10 INSERTION SPECIFICITY [J].
HALLING, SM ;
KLECKNER, N .
CELL, 1982, 28 (01) :155-163
[15]   MUTATIONAL ANALYSIS OF IS10S OUTSIDE END [J].
HUISMAN, O ;
ERRADA, PR ;
SIGNON, L ;
KLECKNER, N .
EMBO JOURNAL, 1989, 8 (07) :2101-2109
[16]  
HUISMAN O, 1987, GENETICS, V116, P185
[17]  
HUISMAN O, 1987, GENETICS, V116, P191
[18]   DNA-SEQUENCE ANALYSIS OF TN10 INSERTIONS - ORIGIN AND ROLE OF 9 BP FLANKING REPETITIONS DURING TN10 TRANSLOCATION [J].
KLECKNER, N .
CELL, 1979, 16 (04) :711-720
[19]  
KLECKNER N, 1979, GENETICS, V92, P1023
[20]  
KLECKNER N, 1991, METHOD ENZYMOL, V204, P139