The Discovery and Assay of RNA Splicing The discovery by Berget and Sharp and by Roberts and co-workers that segments within newly synthesized messenger RNA could be eliminated before the RNA was exported from the nucleus to the cytoplasm was a great surprise. Not only was the enzymology of such a reaction unfamiliar, but the biological need for such a reaction was not apparent. Although splicing is a possible point for cells to regulate expression, there seemed no particular need for utilizing this possibility. One possible reason for splicing could be in the evolution of proteins. Intervening sequences place genetic spacers between coding regions in a gene. As a result, recombination is more likely to occur between coding regions than within them. This permits a coding region to be inherited as an independent module. Not surprisingly then, the portions of proteins that such modules encode often are localized structural domains within proteins. As a result, during the evolution of a protein, domains may be shuffled. It is hard to imagine, however, that this need was great enough to drive the evolution of splicing.

The most plausible explanation for the existence of intervening sequences is that they are the remnants of a parasitic sequence that spread through the genome of some early cell-type. In order that the sequence not inactivate a coding region into which it inserted itself, the coding region arranged that it splice itself out of mRNA. Thus, although the parasitic sequence might have inserted into the middle of an essential gene, the gene was not inactivated. After transcription, and before translation, the RNA copy of the gene containing the sequence was cut and spliced to recover the intact uninterrupted gene. Now that the intervening sequences are there, the cell is beginning to make use of them. One example is regulating the use of alternative splice sites to generate one or another gene product from a single gene.

Both the discovery of messenger splicing and a clear demonstration of splicing used adenovirus RNA. The virus provided a convenient source of DNA for hybridization reactions and RNA extracted from adeno-infected cultured cells was a rich source of viral RNA. Electron microscopy of hybrids formed between adenovirus mRNA and a fragment of the adenovirus genome coding for the coat hexon protein was performed to locate the transcriptional unit. Curiously, the hybrids which formed lacked the expected structure. Many nucleotides at one end of the RNA failed to hybridize to the hexon DNA (Fig. 1). One of the ways splicing was discovered was tracking down the source of this extraneous RNA. Further experiments with longer DNA fragments located DNA complementary to this RNA, but it was far away from the virus hexon gene (Fig. 2). The RNA as extracted from the cells had to have been synthesized, and then cut and spliced several times.

Fig1. RNA-DNA hybrid between a single-stranded fragment of adenovirus DNA and hexon mRNA extracted from cells. The RNA and DNA are not complementary at the 5’ end of the mRNA.

Fig2. Hybridization of adenovirus hexon mRNA to adenovirus DNA from a region well upstream from the hexon gene. The regions a, b, c and d of viral RNA hybridize, but the regions between these segments are missing from the RNA, and the DNA accordingly loops out.

Gel electrophoresis provides a convenient assay to detect splicing and to locate the spliced regions. Hybridization of DNA to messenger RNA that has been spliced to remove introns yields duplexes and loops as shown in Fig. 3. The locations and sizes can be determined by digestion with S1 and ExoVII nucleases followed by electrophoresis on denaturing gels and on gels that preserve the integrity of RNA-DNA duplexes. Since S1 nuclease digests single-stranded RNA and DNA and can act endonucleolytically, it removes all single-stranded or unpaired regions from RNA and DNA. ExoVII, however, digests only single stranded DNA, and only from the ends. This enzyme therefore provides the additional information necessary to determine intron and exon sizes and locations. After digestion with these enzymes, the oligonucleotides can be separated according to size by electrophoresis on polyacrylamide gels. Gels run with normal buffer near neutral pH provide the sizes of the double-stranded duplex molecules, and gels run at alkaline pH provide the molecular weights of the denatured, single-stranded oligonucleotides.

Fig3. Endonuclease S1 is used to digest single-stranded regions of RNA and DNA, and exonuclease Exo VII is used to digest single-stranded DNA exonucleolytically. The DNA is labeled in these experiments. After digestions, electrophoresis on neutral gels analyzes duplexes, and electrophoresis on alkaline gels denatures and analyzes the sizes of fragments.

مواضيع ذات صلة

Involvement of the U1 snRNP Particle in Splicing

البادئ (Promoter)

تضاعف الدنا

The Clinical Utility of Genomics in Hematologic Malignancies

Termination

Polymerase Elongation Rate

فائدة القفازات

الحلزون المزدوج للدنا

تركيب الدنا

Melted DNA Under RNA Polymerase

Measurement of Binding and Initiation Rates

Structural Variation