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Research Article

Early commitment of yeast pre-mRNA to the spliceosome pathway.

P Legrain, B Seraphin, M Rosbash
P Legrain
Department of Biology, Brandeis University, Waltham, Massachusetts 02254.
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B Seraphin
Department of Biology, Brandeis University, Waltham, Massachusetts 02254.
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M Rosbash
Department of Biology, Brandeis University, Waltham, Massachusetts 02254.
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DOI: 10.1128/MCB.8.9.3755
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ABSTRACT

Pre-mRNA splicing in vitro is preceded by complex formation (spliceosome assembly). U2 small nuclear RNA (snRNA) is found in the earliest form of the spliceosome detected by native gel electrophoresis, both in Saccharomyces cerevisiae and in metazoan extracts. To examine the requirements for the formation of this early complex (band III) in yeast extracts, we cleaved the U2 snRNA by oligonucleotide-directed RNase H digestion. U2 snRNA depletion by this means inhibits both splicing and band III formation. Using this depleted extract, we were able to design a chase experiment which shows that a pre-mRNA substrate is committed to the spliceosome assembly pathway in the absence of functional U2 snRNP. Interactions occurring during the commitment step are highly resistant to the addition of an excess of unlabeled substrate and require little or no ATP. Sequence requirements for this commitment step have been analyzed by competition experiments with deletion mutants: both the 5' splice site consensus sequence and the branch point TACTAAC box sequence are necessary. These experiments strongly suggest that the initial assembly process requires a trans-acting factor(s) (RNA and/or proteins) that recognizes and stably binds to the two consensus sequences of the pre-mRNA prior to U2 snRNP binding.

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Early commitment of yeast pre-mRNA to the spliceosome pathway.
P Legrain, B Seraphin, M Rosbash
Molecular and Cellular Biology Sep 1988, 8 (9) 3755-3760; DOI: 10.1128/MCB.8.9.3755

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Early commitment of yeast pre-mRNA to the spliceosome pathway.
P Legrain, B Seraphin, M Rosbash
Molecular and Cellular Biology Sep 1988, 8 (9) 3755-3760; DOI: 10.1128/MCB.8.9.3755
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