IHF modulation of Tn10 transposition: Sensory transduction of supercoiling status via a proposed protein/DNA molecular spring

被引:96
作者
Chalmers, R [1 ]
Guhathakurta, A [1 ]
Benjamin, H [1 ]
Kleckner, N [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1016/S0092-8674(00)81449-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
Architectural protein IHF modulates Tn10 transposition in vitro. IHF stimulates transposon excision. Also, separately, IHF forces transposon end/target DNA interactions into a constrained pathway, "channeling," that yields only unknotted intratransposon inversion circles. Negative supercoiling influences both effects, differently. We infer that IHF is an architectural catalyst: it promotes initial transpososome assembly and is then ejected from the transpososome. IHF then rebinds, altering transpososome conformation to promote channeling. We also infer that the developing transpososome is a molecular spring: DNA provides basic elasticity; a conformational change in transposase provides force; and IHF and/or supercoiling provide conformational inputs. In vivo, IHF is a sensory transducer of chromosomal supercoiling status: with supercoiling absent, IHF is "supercoiling relief factor"; with supercoiling present, stimulation and channeling comprise a homeostatic pair such that modest changes in chromosome condition strongly influence transpositional outcome.
引用
收藏
页码:897 / 908
页数:12
相关论文
共 28 条
[1]   INTRAMOLECULAR TRANSPOSITION BY TN10 [J].
BENJAMIN, HW ;
KLECKNER, N .
CELL, 1989, 59 (02) :373-383
[2]   Contributions of supercoiling to Tn3 resolvase and phage Mu Gin site-specific recombination [J].
Benjamin, KR ;
Abola, AP ;
Kanaar, R ;
Cozzarelli, NR .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 256 (01) :50-65
[3]   USE OF SITE-SPECIFIC RECOMBINATION AS A PROBE OF DNA-STRUCTURE AND METABOLISM INVIVO [J].
BLISKA, JB ;
COZZARELLI, NR .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 194 (02) :205-218
[4]   The three chemical steps of Tn10/IS10 transposition involve repeated utilization of a single active site [J].
Bolland, S ;
Kleckner, N .
CELL, 1996, 84 (02) :223-233
[5]   DNA bending and the initiation of transcription at sigma(54)-dependent bacterial promoters [J].
Carmona, M ;
ClaverieMartin, F ;
Magasanik, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (18) :9568-9572
[6]   CELL CYCLE-SPECIFIC CHANGES IN NUCLEOPROTEIN COMPLEXES AT A CHROMOSOMAL REPLICATION ORIGIN [J].
CASSLER, MR ;
GRIMWADE, JE ;
LEONARD, AC .
EMBO JOURNAL, 1995, 14 (23) :5833-5841
[7]   IS10 Tn10 transposition efficiently accommodates diverse transposon end configurations [J].
Chalmers, RM ;
Kleckner, N .
EMBO JOURNAL, 1996, 15 (18) :5112-5122
[8]  
HUISMAN O, 1989, EMBO J, V8, P211
[9]   Mechanism of site-specific DNA inversion in bacteria [J].
Johnson, Reid C. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1991, 1 (03) :404-411
[10]  
KLECKNER N, 1990, GENETICS, V124, P449