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1.
J Mol Biol ; 266(4): 665-76, 1997 Mar 07.
Article in English | MEDLINE | ID: mdl-9102460

ABSTRACT

Carbon catabolite repression (CCR) of several operons in Bacillus subtilis and Bacillus megaterium is mediated by the cis-acting cre sequence and trans-acting catabolite control protein (CcpA). We describe purification of CcpA from B. megaterium and its interaction with regulatory sequences from the xyl operon. Specific interaction of CcpA with cre as scored by DNase I footprints at concentrations similar to the in vivo situation requires the presence of effectors. We have found two molecular effectors for CcpA activity, which lead to different recognition modes of DNA. The heat-stable phosphotransfer protein HPr from the PTS sugar uptake system triggers non-cooperative binding of CcpA to cre when phosphorylated at Ser46 (HPr-Ser46-P). Glucose 6-phosphate (Glc-6-P) triggers cooperative binding of CcpA to cre and two auxiliary cre* sites, one of which overlaps the -35 box of the xyl promoter. Binding to cre* depends on the presence of the functional cre sequence. A mutation in cre abolishes carbon catabolite repression in vivo and binding of CcpA to cre and cre* in vitro, indicating looping of the intervening DNA. The two triggers are not simultaneously active. The acidity of the buffer determines which of them activates CcpA when both are present in vitro. Glc-6-P is preferred at pH values below 5.4, and HPr-Ser46-P is preferred at neutral pH. The Ccpa dimers present at neutral pH form tetramers and higher oligomers at pH 4.6, explaining cooperativity of binding to DNA. CcpA is the first member of the LacI/GalR family of regulators, for which oligomerization without the leucine zipper at the C terminus is demonstrated.


Subject(s)
Bacillus megaterium/metabolism , DNA, Bacterial/metabolism , DNA-Binding Proteins/metabolism , Operator Regions, Genetic , Repressor Proteins/metabolism , Bacillus megaterium/genetics , Bacterial Proteins/metabolism , DNA Footprinting , DNA, Recombinant , DNA-Binding Proteins/isolation & purification , Electrophoresis, Polyacrylamide Gel , Gene Expression Regulation, Bacterial , Genes, Bacterial/genetics , Glucose/pharmacology , Glucose-6-Phosphate/pharmacology , Hydrogen-Ion Concentration , Luciferases/genetics , Luciferases/metabolism , Mutation/genetics , Operon/genetics , Phosphoenolpyruvate Sugar Phosphotransferase System/pharmacology , Phosphorylation , Promoter Regions, Genetic , Repressor Proteins/isolation & purification
2.
Mol Cell Biol ; 12(1): 229-39, 1992 Jan.
Article in English | MEDLINE | ID: mdl-1309589

ABSTRACT

Different Dictyostelium discoideum strains contain between 2 and 200 copies of a retrotransposable element termed DRE (Dictyostelium repetitive element). From the analysis of more than 50 elements, it can be concluded that DRE elements always occur 50 +/- 3 nucleotides upstream of tRNA genes. All analyzed clones contain DRE in a constant orientation relative to the tRNA gene, implying orientation specificity as well as position specificity. DRE contains two open reading frames which are flanked by nonidentical terminal repeats. Long terminal repeats (LTRs) are composed of three distinct modules, called A, B, and C. The tRNA gene-proximal LTR is characterized by one or multiple A modules followed by a single B module (AnB). With respect to the distal LTR, two different subforms of DRE have been isolated. The majority of isolated clones contains a distal LTR composed of a B module followed by a C module (BC), whereas the distal LTR of the other subform contains a consecutive array of a B module, a C module, a slightly altered A module, another B module, and another C module (BC.ABC). Full-length as well as smaller transcripts from DRE elements have been detected, but in comparison with the high copy number in D. discoideum strains derived from the wild-type strain NC4, transcription is rather poor.


Subject(s)
DNA Transposable Elements , Dictyostelium/genetics , RNA, Transfer/genetics , Repetitive Sequences, Nucleic Acid , Amino Acid Sequence , Animals , Base Sequence , DNA , Genome , Molecular Sequence Data , Open Reading Frames , Restriction Mapping , Sequence Alignment
3.
J Mol Biol ; 222(3): 537-52, 1991 Dec 05.
Article in English | MEDLINE | ID: mdl-1660925

ABSTRACT

A total of 68 different tRNA genes from the cellular slime mold Dictyostelium discoideum have been isolated and characterized. Although these tRNA genes show features common to typical nuclear tRNA genes from other organisms, several unique characteristics are apparent: (1) the 5'-proximal flanking region is very similar for most of the tRNA genes; (2) more than 80% of the tRNA genes contain an "ex-B motif" within their 3'-flanking region, which strongly resembles characteristics of the consensus sequence of a T-stem/T-loop region (B-box) of a tRNA gene; (3) probably more than 50% of the tRNA genes in certain D. discoideum strains are associated with a retrotransposon, termed DRE (Dictyostelium repetitive element), or with a transposon, termed Tdd-3 (Transposon Dictyostelium discoideum). DRE always occurs 50 (+/- 3) nucleotides upstream and Tdd-3 always occurs 100 (+/- 20) nucleotides downstream from the tRNA gene. D. discoideum tRNA genes are organized in multicopy gene families consisting of 5 to 20 individual genes. Members of a particular gene family are identical within the mature tRNA coding region while flanking sequences are idiosyncratic.


Subject(s)
Dictyostelium/genetics , RNA, Transfer/genetics , Regulatory Sequences, Nucleic Acid/genetics , Repetitive Sequences, Nucleic Acid/genetics , Animals , Base Sequence , Codon/genetics , DNA Transposable Elements , DNA, Protozoan/genetics , DNA, Single-Stranded , Exons , Introns , Molecular Sequence Data , Multigene Family , Sequence Homology, Nucleic Acid
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