Intragenic suppressors of induction-deficient TetR mutants: Localization and potential mechanism of action

被引:5
作者
Biburger, M [1 ]
Berens, C [1 ]
Lederer, T [1 ]
Krec, T [1 ]
Hillen, W [1 ]
机构
[1] Univ Erlangen Nurnberg, Inst Mikrobiol Biochem & Genet, Lehrstuhl Mikrobiol, D-91058 Erlangen, Germany
关键词
D O I
10.1128/JB.180.3.737-741.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Eight Tn10 Tet repressor mutants with an induction-deficient phenotype and with primary mutations located at or close to the dimer interface were mutagenized and screened for inducibility in the presence of tetracycline, The second-site suppressors with wild-type-like operator binding activity that were obtained act, except for one, at a distance, suggesting that they contribute to conformational changes in the Tet repressor. Many of these long-range suppressors occur along the dimer interface, indicating that interactions between the monomers play an important role in Tet repressor induction.
引用
收藏
页码:737 / 741
页数:5
相关论文
共 30 条
[1]   A THREONINE TO ALANINE EXCHANGE AT POSITION-40 OF TET REPRESSOR ALTERS THE RECOGNITION OF THE 6TH BASE PAIR OF TET OPERATOR FROM GC TO AT [J].
ALTSCHMIED, L ;
BAUMEISTER, R ;
PFLEIDERER, K ;
HILLEN, W .
EMBO JOURNAL, 1988, 7 (12) :4011-4017
[2]   CONTACTS BETWEEN TET REPRESSOR AND TET OPERATOR REVEALED BY NEW RECOGNITION SPECIFICITIES OF SINGLE AMINO-ACID REPLACEMENT MUTANTS [J].
BAUMEISTER, R ;
HELBL, V ;
HILLEN, W .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 226 (04) :1257-1270
[3]  
BERENS C, 1992, J BIOL CHEM, V267, P1945
[4]   The role of the variable region in Tet repressor for inducibility by tetracycline [J].
Berens, C ;
Schnappinger, D ;
Hillen, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (11) :6936-6942
[5]   DELETION MUTAGENESIS OF TN10 TET REPRESSOR - LOCALIZATION OF REGIONS IMPORTANT FOR DIMERIZATION AND INDUCIBILITY IN-VIVO [J].
BERENS, C ;
PFLEIDERER, K ;
HELBL, V ;
HILLEN, W .
MOLECULAR MICROBIOLOGY, 1995, 18 (03) :437-448
[6]   STRUCTURAL REQUIREMENTS OF TETRACYCLINE-TET REPRESSOR INTERACTION - DETERMINATION OF EQUILIBRIUM BINDING CONSTANTS FOR TETRACYCLINE ANALOGS WITH THE TET REPRESSOR [J].
DEGENKOLB, J ;
TAKAHASHI, M ;
ELLESTAD, GA ;
HILLEN, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (08) :1591-1595
[7]   GENETIC-ANALYSIS OF THE FOLDED STRUCTURE OF YEAST MITOCHONDRIAL CYTOCHROME-B BY SELECTION OF INTRAGENIC 2ND-SITE REVERTANTS [J].
DIRAGO, JP ;
HERMANNLEDENMAT, S ;
RISLER, FPJ ;
NETTER, P ;
SLONIMSKI, PP .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 248 (04) :804-811
[8]   NONINDUCIBLE TET REPRESSOR MUTATIONS MAP FROM THE OPERATOR BINDING MOTIF TO THE C-TERMINUS [J].
HECHT, B ;
MULLER, G ;
HILLEN, W .
JOURNAL OF BACTERIOLOGY, 1993, 175 (04) :1206-1210
[9]  
HELBL V, 1993, CURR TOPICS MOL GENE, V1, P123
[10]   MECHANISMS UNDERLYING EXPRESSION OF TN10 ENCODED TETRACYCLINE RESISTANCE [J].
HILLEN, W ;
BERENS, C .
ANNUAL REVIEW OF MICROBIOLOGY, 1994, 48 :345-369