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Analysis of ribozyme structure and function by nucleotide analog interference mapping.

Nucleotide analog interference mapping (NAIM) is a quick and effective method to define concurrently, yet singly, the importance of specific functional groups at particular nucleotide residues in relation to the structure and function of an RNA. NAIM can be utilized on virtually any RNA with an assayable function, including catalytic RNAs. The method hinges on the ability to successfully incorporate, within an RNA transcript, various 5'-O-(1-thio)nucleoside analogs randomly via in vitro transcription. This can be achieved by using wild-type or Y639F mutant T7 RNA polymerase, thus creating a pool of analog-doped RNAs. When subjected to a selection step to separate the active transcripts from the inactive ones, the pool helps to identify functional groups that are crucial for RNA activity. The technique can be used to study ribozyme structure and function via monitoring of cleavage or ligation reactions, or define functional groups that are critical for RNA folding, RNA-RNA interactions, and RNA interactions with proteins, metals, or other small molecules. All major classes of catalytic RNAs have been examined by NAIM. This is a generalized approach that should provide the scientific community with the tools to better understand the RNA structure-activity relationship (SAR).

Base Sequence↗

SR protein kinases: the splice of life.

The eukaryotic genome codes for most of its proteins though discontinuous coding sequences called exons, which are separated by noncoding sequences known as introns. Following transcription of a gene, these exons must be spliced precisely, removing the intervening introns, to form meaningful mature messenger RNAs (mRNA) that are transported to the cytoplasm and translated by the ribosomal machinery. To add yet another level of complexity, a process known as alternative splicing exists, whereby a single pre-mRNA can give rise to two or more mature mRNAs depending on the combination of exons spliced together. Alternative splicing of pre-mRNAs is emerging as an important mechanism for gene regulation in many organisms. The classic example of splicing as a regulator of genetic information during a developmental process is sex determination in Drosophila. The now well-characterized cascade of sex-specific alternative splicing events demonstrates nicely how the control of splice site selection during pre-mRNA processing can have a profound effect on the development of an organism. The factors involved in pre-mRNA splicing and alternative splice site selection have been the subject of active study in recent years. Emerging from these studies is a picture of regulation based on protein-protein, protein-RNA, and RNA-RNA interactions. How the interaction of the various splicing constituents is controlled, however, is still poorly understood. One of the mechanisms of regulation that has received attention recently is that of posttranslational phosphorylation. In the following article, we cite the evidence for a role of phosphorylation in constitutive and alternative splicing and discuss some of the recent information on the biochemistry and biology of the enzymes involved.

Alternative Splicing↗

Host defenses to parasitic sequences and the evolution of epigenetic control mechanisms.

The analysis of transgene silencing effects in plants and other eukaryotic organisms has revealed novel mechanisms of epigenetic regulation that are based on recognition of nucleic acid sequence homology. These homology-dependent gene silencing phenomena are characterized by an inverse relationship between copy number of a particular sequence and expression levels. Depending on whether promoter regions or transcribed sequences are repeated, silencing occurs at the transcriptional or post-transcriptional level, respectively. Different silencing effects involving DNA-DNA or RNA-DNA associations in the nucleus, and RNA-RNA interactions in the cytoplasm appear to reflect distinct host defense responses to parasitic sequences, including transposable elements (TEs), viroids and RNA viruses. Natural epigenetic phenomena that resemble transgene silencing effects often involve endogenous genes comprising recognizable TE sequences or rearrangements generated by TEs and can thus be interpreted in terms of host defense systems. A genome defense that inactivates TEs by methylation might have been recruited during evolution to regulate the transcription of plant and vertebrate genes that contain remnants of TE insertions in promoter regions.

DNA Methylation↗

[Study of ribosome structure using the biochemical methods: judgment day].

The data on RNA-RNA interactions between the components of the E. coli translation machinery obtained by X-ray crystallography and chemical methods are compared. The approaches to the study of RNA secondary and tertiary structure are assessed. The following conclusions are made: comparative sequence analysis and compensatory mutations approach both give reliable data on the RNA secondary structure. The chemical modification technique provides good results. Local cleavage of internucleotide bonds by hydroxyl radicals is reliable in the frame of its 40 A resolution, in contrast to the application of copper-phenanthroline complex as a cleavage reagent, which is unreliable. Direct UV irradiation and nitrogen mustard treatment are the best methods of crosslink generation. In vitro transcription is the only good method for the incorporation of nucleotide analogs in RNA. RNase H hydrolysis and/or nucleotide-specific RNases fingerprints must be applied for the crosslink site determination in parallel with reverse transcription.

Base Sequence↗

[Region of intermolecular complementarity in Escherichia coli 16S rRNA, mRNA, and tRNA molecules].

The results of computer analysis of complementarity regions in the sequences of E. coli 16S rRNA, mRNAs and tRNAs are reported in this article. The potential regions of intermolecular RNA-RNA hybridization, or clinger fragments, in 16S rRNA, which are complementary to the sites frequently occurring in mRNAs and tRNAs, were found. Major clinger fragments on 16S rRNA are universal for genes that belong to different functional groups. Our results show there are adaptations of the structural organization of the 16S rRNA molecule to messenger and transport RNA sequences. RNA interaction with clinger fragments may contribute to upregulation of translation process through increasing the local concentration of mRNAs and tRNAs in the vicinity of the ribosome and their proper positioning, as well as decrease the efficiency of translation through non-specific mRNA-16SrRNA interactions.

Escherichia coli↗

Noncoding RNA transcripts.

Recent analyses of the human genome and available data about the other higher eukaryotic genomes have revealed that, in contrast to Eubacteria and Archaea, only a small fraction of the genetic material (ca 1.5%) codes for proteins. Most of genomic DNA and its RNA transcripts are involved in regulation of gene expression, which can be exerted at either the transcriptional level, controlling whether a gene is transcribed and to what extent, or at the post-translational level, regulating the fate of the transcribed RNA molecules, including their stability, efficiency of their translation and subcellular localization. Noncoding RNA genes produce functional RNA molecules (ncRNAs) rather than encoding proteins. These stable RNAs act by multiple mechanisms such as RNA-RNA base pairing, RNA-protein interactions and intrinsic RNA activity, as well as regulate diverse cellular functions, including RNA processing, mRNA stability, translation, protein stability and secretion. Non-protein-coding RNAs are known to play significant roles. Along with transfer RNAs, ribosomal RNAs and mRNAs, ncRNAs contribute to gene splicing, nucleotide modification, protein transport and regulation of gene expression.

Animals↗

Mechanism of ribosomal subunit association: oligodeoxynucleotides as probes.

From the kethoxal treatment data [Herr, W.; Chapman, N.M.; Noller, H.F. (1979) J. Mol. Biol. 130, 433-439] some regions of ribosomal RNAs are thought to be responsible for the association of 30S and 50S ribosomes of E. coli to form 70S ribosomes. In order to test this possibility about a dozen oligodeoxynucleotides complementary to the suspected regions of rRNAs were synthesised. Their association with ribosomes and naked rRNAs was tested by the gel filtration technique. In order to check the effects on the ribosomal subunit association or rRNA association either intact 30S and 50S ribosomes or naked 16S and 23S rRNAs were preincubated with the individual oligodeoxynucleotide and its effect was checked by density gradient centrifugation followed by UV absorbance monitoring. Some oligodeoxynucleotides interfered with either subunit association or 16S RNA and 23S RNA association, some with both. These data clearly indicate that RNA-RNA interaction plays the major role in ribosomal subunit association.

Base Sequence↗

IRIS: intermolecular RNA interaction search.

Here we present IRIS, a method for prediction of RNA-RNA interactions that is based on dynamic programming and extends current RNA secondary structure prediction approaches. Using this method we have found a number of interesting refinements to the structures of RNA-RNA complexes that have been studied previously and predicted novel targets for several known regulatory RNAs in E. coli. The computational time and memory usage of IRIS are O(n(3)m(3)) and O(n(2)m(2)), respectively, where n and m are the lengths of the input sequences. IRIS can be used for analysis of antisense regulatory systems in sequenced organisms and for the design of artificial riboregulators such as antisense drugs.

Base Sequence↗

Secondary structure of the RNA component of a nuclear/mitochondrial ribonucleoprotein.

RNase mitochondrial RNA processing (MRP) is a site-specific endoribonuclease located in both the nucleus and mitochondria of vertebrate cells. The enzyme is a ribonucleoprotein whose RNA component has been shown to be encoded by a nuclear gene. Because RNase MRP is particular in its substrate requirement, RNA-RNA interaction has been proposed as important for the cleavage reaction. A secondary structure of this RNA from mouse cells has been derived by chemical modification of in vivo MRP RNA in ribonucleoprotein form, as isolated free RNA, and as RNA synthesized in vitro. Full-length MRP RNA appears to adopt a conformation containing a significant number of single-stranded residues and may form a pseudoknot. The data are consistent with both the RNA within the ribonucleoprotein and the free RNA possessing comparable secondary structures and suggest a possible site of interaction between enzyme and substrate. The human MRP RNA can be folded into a conformation very similar to that predicted for the mouse MRP RNA. A more limited analysis of human MRP RNA is consistent with the structure proposed for the mouse species.

Animals↗

Regulation of immediate early gene expression by exercise: short cuts for the adaptation of immune function.

Onset of physical activity induces a wide variety of rapid biophysical and biochemical responses that act on cells and lead to a wide range of phenotypic adaptations. Here we elucidate the role of immediate early gene (IEG) expression as a first line of transcriptional response that mediates protein neosynthesis and leads to adaptation of immune function. New posttranscriptional mechanisms have been described that speed up transcriptional responses. These include RNA-RNA interactions such as those exploited by miRNAs and stimulus-dependent cytoplasmic polyadenylation. We describe these shortcuts that modulate expression and discuss the challenges of accurately measuring them using various transcriptomic screening and quantification approaches. Although there is high complexity of the upstream as well as the downstream pathways that lead to IEG expression, IEG expression itself may only show a limited number of response patterns. Focusing transcriptomic approaches in exercise immunology at the IEG-level may facilitate the discovery of exercise-specific transcriptional signatures.

Adaptation, Physiological↗

[Role of ribonucleic acids in organizing the structure of Escherichia coli ribosomes].

The paper summarizes recent data on the secondary and tertiary structure of RNA in ribosomes. The participation of RNA in intraribosomal interactions and the role of these interactions in organization of ribosomal subunits are discussed. The following conclusions are made: 1) the structure of ribosomal subunits is predominantly created with their RNA components; 2) RNA molecules in ribosomal subunits have a very compact structure; the formation of this structure is followed by the rearrangement of the secondary structure of RNA; 3) the small group of ribosomal proteins plays an important role in the folding of RNA in the compact conformation: they not only stabilize intraribosomal RNA conformation but probably induce new RNA-RNA contacts.

Bacterial Proteins↗

[Compact structure of the small E. coli ribosomal subunit and its RNA studied by fluorescence spectroscopy and sedimentation analysis].

Analysis of the temperature dependence of fluorescence polarization of ethidium bromide adsorbed on the double helical fragments of 16S RNA's hairpin loops was used to characterize the intramolecular flexibility of RNA in the free state and within 30S subunit. We show that the local mobility of RNA segments is strongly limited by the tertiary structure of 16S RNA and ribosomal proteins reinforce these limitations. It was suggested that the mechanism of the temperature dependent RI particle activation involved the temporary increase of the local mobility of RNA segments in RNP which favored the formation of the new intraribosomal contacts. A comparison of sw 20 dependences of RNA and 30S subunit on Mg+ and K+ concentrations leads to the proposal that RNA in the small subunit in the physiological conditions has the stressed conformation. This conformation is maintained by the Mg2+-dependent RNA-RNA interactions induced by ribosomal proteins and specific only for the subunit.

Escherichia coli↗

[Possible role of tRNA1Lys in recognition of pre-mRNA sequences involved in the control of splicing].

Previously we presented some evidence for involvement of the imported tRNA1Lys in splicing the mitochondrial mosaic genes transcripts in yeast. The new data provided here together with our previous results show that tRNA1Lys/transcripts complementarity permits accurate prediction of intron-exon donor boundaries for at least 7 (probably all 9) Dujonian 1st class introns. A computer-assisted search for homologies between mosaic genes transcripts and sequences complementary to tRNA1Lys reveals most of the control sequences previously determined as the sites of 1) cis-acting splicing blocks, 2) conserved RNA sequences and 3) conserved features of transcripts secondary structure. The sequences revealed in our study are as follows: sequences GGGGG and GGCTC in 2nd class introns and less convincing cases are R + E', E + P and IG in 1st class introns. The results obtained here together with the results of other authors suggest a series of (often weak) alternative RNA-RNA interactions needed to regulate and(or) provide a sufficiently error-free mechanism of splicing for the mosaic genes transcripts. A comparison was made of: 1) sequences near the sites of 2 different autocatalytic Tetrahymena pre-rRNA cleavage-ligation events (splicing and cyclization of the intron RNA) and 2) sequences of tRNA1Lys probably contacting donor boundaries of 1st class mitochondrial introns. The comparison reveals an obvious conservation of some basic structure regardless of the different chemical directions of the strands involved. The result suggests a possible catalytic function for the tRNA1Lys probably involved also in recognition and control processes of mitochondrial transcripts splicing.

Base Sequence↗

RNA structural patterns and splicing: molecular basis for an RNA-based enhancer.

Efficient splicing of the 325-nt yeast (Saccharomyces cerevisiae) rp51b intron requires the presence of two short interacting sequences located 200 nt apart. We used the powerful technique of randomization-selection to probe the overall structure of the intron and to investigate its role in pre-mRNA splicing. We identified a number of alternative RNA-RNA interactions in the intron that promote efficient splicing, and we showed that similar base pairings can also improve splicing efficiency in artificially designed introns. Only a very limited amount of structural information is necessary to create or maintain such a mechanism. Our results suggest that the base pairing contributes transiently to the spliceosome assembly process, most likely by complementing interactions between splicing factors. We propose that splicing enhancement by structure represents a general mechanism operating in large yeast introns that evolutionarily preceded the protein-based splicing enhancers of higher eukaryotes.

Base Sequence↗

Nuclease activities of Moloney murine leukemia virus reverse transcriptase. Mutants with altered substrate specificities.

RNases H are traditionally thought to degrade RNA only in RNA-DNA hybrid form. We found that the wild-type Moloney murine leukemia virus (M-MuLV) reverse transcriptase (RT) was capable of degrading RNA in RNA-RNA duplexes as well as in RNA-DNA hybrids, as assayed by in situ gel techniques. Escherichia coli RNase H does not degrade the RNA-RNA duplex in this assay, while E. coli RNase III, a double-strand-specific ribonuclease, does. The apparent specific activity of M-MuLV RT on RNA-RNA duplexes is similar to that on RNA-DNA hybrids. Neither the DNA polymerase domain nor the RNase H domain of RT expressed individually exhibited this RNA-RNA activity. We have generated a series of mutations in the RNase H domain of M-MuLV RT, expressed the mutant enzymes in E. coli, and assayed these mutants for various activities. All RTs were as active as the wild type in the oligo(dT):poly(rA) DNA polymerase assay, and many retained both nuclease activities. Two enzymes with mutations at the carboxyl terminus of the RNase H domain retained RNA-DNA activity, but not RNA-RNA activity. Another mutant enzyme showed the opposite phenotype, retaining RNA-RNA, but not RNA-DNA, nuclease activity. Thus, we were able to genetically separate the two activities. These results may be helpful in defining enzyme-substrate interactions.

Blotting, Western↗

Coronavirus: how a large RNA viral genome is replicated and transcribed.

Coronaviruses are important human and animal pathogens and contain an extraordinarily long (27-31 kb) RNA genome. Its RNA synthesis involves complex mechanisms of regulation, similar to those of DNA viruses. In this treatise, mouse hepatitis virus (MHV) is used as a model for the discussion of the mechanism of viral RNA synthesis. We show that MHV RNA synthesis requires interactions of multiple RNA components, which are likely mediated by protein-RNA and protein-protein, as well as RNA-RNA, interactions. This virus also provides a unique example of a discontinuous transcription mechanism, which involves a trans-acting RNA component. Finally, study of the cis-acting signals for the various steps of RNA synthesis revealed an insight into the regulation of viral RNA synthesis. This discussion suggests that the regulation of RNA synthesis in coronavirus is more complex than previously thought possible for RNA viruses. Coronavirus RNA transcription and replication may serve as a paradigm of RNA synthesis for RNA viruses in general.

Animals↗

Three dimensional model for the 16S ribosomal RNA in the Escherichia coli ribosome.

Molecular modeling has been performed to help correct and refine an approximate three dimensional structure for Eschericia coli 16S rRNA that originated as hand-built wire model. The wire model was built to accommodate the base pairs in 16S rRNA (1), mRNA.16S rRNA interactions (2,3), rRNA.ribosomal protein interactions (see 4), ribosomal protein-ribosomal protein distances (5), intramolecular RNA-RNA UV-crosslinks (6,7) and site-directed mutagenesis experiments (8). In the computer model, individual base-paired regions were constructed separately and then were installed into the expected locations to produce the entire structure. We describe here the considerations, steps and results of this refinement process.

Computer Simulation↗

Three dimensional model for the 16S ribosomal RNA that incorporates information for the mRNA track.

A three dimensional model for the 16S rRNA in the ribosome is described that accommodates information for mRNA.16S rRNA interactions as well as accommodating information that has been used as constraints for determining the internal 16S rRNA structure. mRNA.16S rRNA interactions have been summarized from experiments that employ photoaffinity crosslinking to identify sites at which the mRNA comes into close contact with the 16S rRNA. The mRNA track that has been constructed follows a path completely around the middle of the 30S subunit, occupying a space above 16S rRNA domains I and II and below 16S rRNA domain III. The mRNA track contains regions associated with contacts with the 16S rRNA in, and just upstream of, the P tRNA site, associated with contacts around the A site and associated with neighborhoods upstream of the Shine-Dalgarno region and downstream of the decoding region. Structural constraints that come from UV-induced RNA-RNA crosslinks, suggest that the mRNA decoding region lies in a groove between three 16S rRNA duplex regions facing the 50S subunit.

Base Sequence↗