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A possible regulatory mechanism in RNA processing and its implication for posttranscriptional sequence control during
Abstract:
1. This paper is concerned with the possible molecular mechanism for RNA processing including posttranscriptional sequence control underlying the differentiation of cell functions. 2. It was previously postulated that intramolecular double-stranded hairpin structures present at 5'- and 3'-terminal regions of a 'pre-mRNA' are key elements for RNA splicing [24]. 3. In this paper the possibility is considered that the splicing of 'pre-mRNA' can be regulated in such a way that the formation of the proper double-stranded hairpin structures is prevented by the binding of low-molecular-weight nuclear RNA (LnRNA) to the terminal regions and/or to the nucleotide sequences around the exon-intron and intron-exon joint sites of the 'pre-mRNA' molecules. 4. Complementarity assessment of nucleotide sequences of rat preproinsulin 'pre-mRNA' and rat LnRNA, i.e. Ul, showed that Ul RNA is capable of forming stable double-standard intermolecular structures around the joint sites of preproinsulin 'pre-mRNA' and may prevent the formation of intramolecular double-stranded structures required for RNA splicing. This may imply a regulatory (inhibitory) role for Ul RNA in the processing of 'pre-mRNA'. 5. A possible regulatory role of LnRNA in RNA splicing is discussed in relation to the determination of the mRNA population to be translated in the cytoplasm during differentiation of cell functions.