33 research outputs found
Precursors to 16S and 23S ribosomal RNA from a ribonuclease III− strain of Escherichia coli contain intact RNase III processing sites
This is the published version. Copyright 1980 by the Oxford University Press. All rights reserved.Escherichia coli cells lacking the ribosomal RNA processing enzyme RNase III do not excise the normal RNA precursors pl6a (17S) and p23a from nascent rRNA transcripts. These cells produce, instead, slightly larger pl6b and p23b precursors. Digestion of pl6b or p23b rRNA with RNases A plus Tl yields double-stranded fragments composed of sequences located at both the 5′ and the 3′ end regions of the molecules. The terminal duplex, or stem, of p 16b contains sequences surrounding the site of RNase III processing which in wild-type cells produces pl6a rRNA: the p23b stem likewise contains an intact RNase III cleavage site. The results confirm our earlier prediction for the structure of rRNA transcripts, and also yield a definite secondary structure for the pl6 stem, which was not uniquely determined by the corresponding DNA sequence. These experiments demonstrate the absence of significant RNase III processing activity in rnc-105 strains of E. coli, and implicate the participation of another endonuclease(s) 1n rRNA processing in mutant and wild-type cells
Adjacent single-stranded regions mediate processing of tRNA precursors by RNase E direct entry
The RNase E family is renowned for being central to
the processing and decay of all types of RNA in
many species of bacteria, as well as providing the
first examples of endonucleases that can recognize
50
-monophosphorylated ends thereby increasing
the efficiency of cleavage. However, there is
increasing evidence that some transcripts can be
cleaved efficiently by Escherichia coli RNase E via
direct entry, i.e. in the absence of the recognition of
a 50
-monophosphorylated end. Here, we provide
biochemical evidence that direct entry is central to
the processing of transfer RNA (tRNA) in E. coli, one
of the core functions of RNase E, and show that it is
mediated by specific unpaired regions that are
adjacent, but not contiguous to segments cleaved
by RNase E. In addition, we find that direct entry at a
site on the 50 side of a tRNA precursor triggers a
series of 50
-monophosphate-dependent cleavages.
Consistent with a major role for direct entry
in tRNA processing, we provide additional evidence
that a 50
-monophosphate is not required to
activate the catalysis step in cleavage. Other
examples of tRNA precursors processed via direct
entry are also provided. Thus, it appears increasingly
that direct entry by RNase E has a major role
in bacterial RNA metabolism
Diversity of 16S-23S rDNA Internal Transcribed Spacer (ITS) Reveals Phylogenetic Relationships in Burkholderia pseudomallei and Its Near-Neighbors
Length polymorphisms within the 16S-23S ribosomal DNA internal transcribed spacer (ITS) have been described as stable genetic markers for studying bacterial phylogenetics. In this study, we used these genetic markers to investigate phylogenetic relationships in Burkholderia pseudomallei and its near-relative species. B. pseudomallei is known as one of the most genetically recombined bacterial species. In silico analysis of multiple B. pseudomallei genomes revealed approximately four homologous rRNA operons and ITS length polymorphisms therein. We characterized ITS distribution using PCR and analyzed via a high-throughput capillary electrophoresis in 1,191 B. pseudomallei strains. Three major ITS types were identified, two of which were commonly found in most B. pseudomallei strains from the endemic areas, whereas the third one was significantly correlated with worldwide sporadic strains. Interestingly, mixtures of the two common ITS types were observed within the same strains, and at a greater incidence in Thailand than Australia suggesting that genetic recombination causes the ITS variation within species, with greater recombination frequency in Thailand. In addition, the B. mallei ITS type was common to B. pseudomallei, providing further support that B. mallei is a clone of B. pseudomallei. Other B. pseudomallei near-neighbors possessed unique and monomorphic ITS types. Our data shed light on evolutionary patterns of B. pseudomallei and its near relative species
Spatial configuration of ribosomal proteins: A computer-generated model of the 30S subunit
Genetic approaches to the study of ribosomes
Specific mutants of Escherichia coli have been used in order to investigate certain aspects of ribosome function, bio synthesis and decay. These studies show that in the function of the ribosome its various components are very interdependent and cooperative. It was possible to demonstrate that a binding site for erythromycin, which is on the 50S ribosomal subunit, could be affected by alterations in the 30S ribosomal subunit. The alterations are in ribosome proteins as well as in 16S rRNA. On the other hand, a mutational alteration, probably in the 16S rRNA, blocks ribosome maturation but at a relatively late stage. This alteration leads to cell death. The maturation cleavages of rRNAs were investigated in as train lacking RNase III, a specific enzyme which cleaves out p16 and p23 from the growing rRNA transcript. These studies suggest that at least three ribonucleases participate in the primary processing (during transcription), while at least three other ribonucleases participate in the secondary processing, which leads to the final mature rRNA molecules. When cells stop growing exponentially, decay of ribosome stakes place. By analyzing the process in mutants lacking or containing altered ribonucleases, it was possible to elucidate a mechanism for this turnover. The process starts by an endonucleolytic attack on the rRNA in the ribosomal subunits. After such an attack the ribosome disintegrates to fragments of RNA and ribosomal proteins, both of which can be further decayed to soluble material. Two endoribonucleases were identified in cell extracts which could be the enzymes which initiate this important turnover process.DAVID APIRION, Department of Microbiology and Immunology, Washington University School of Medicine, St. Louis, Missouri