Interaction of U6 snRNA with a sequence required for function of the nematode SL RNA in trans-splicing

Nematode trans-spliced leader (SL) RNAs are composed of two domains, an exon [the 22-nucleotide spliced leader] and a small nuclear RNA (snRNA)-like sequence. Participation in vitro of the spliced leader RNA in trans-splicing reactions is independent of the exon sequence or size and instead depends...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 1992-12, Vol.258 (5089), p.1775-1780
Hauptverfasser: Hannon, G.J. (Cold Spring Harbor Laboratory, Cold Spring Harbor, NY), Maroney, P.A, Yu, Y.T, Hannon, G.E, Nilsent, T.W
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container_end_page 1780
container_issue 5089
container_start_page 1775
container_title Science (American Association for the Advancement of Science)
container_volume 258
creator Hannon, G.J. (Cold Spring Harbor Laboratory, Cold Spring Harbor, NY)
Maroney, P.A
Yu, Y.T
Hannon, G.E
Nilsent, T.W
description Nematode trans-spliced leader (SL) RNAs are composed of two domains, an exon [the 22-nucleotide spliced leader] and a small nuclear RNA (snRNA)-like sequence. Participation in vitro of the spliced leader RNA in trans-splicing reactions is independent of the exon sequence or size and instead depends on features contained in the snRNA-like domain of the molecule. Chemical modification interference analysis has revealed that two short sequence elements in the snRNA-like domain are necessary for SL RNA activity. These elements are sufficient for such activity because when added to a 72-nucleotide fragment of a nematode U1 snRNA, this hybrid RNA could participate in trans-splicing reactions in vitro. One of the critical sequence elements may function by base-pairing with U6 snRNA, an essential U snRNA for both cis- and trans-splicing
doi_str_mv 10.1126/science.1465612
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Participation in vitro of the spliced leader RNA in trans-splicing reactions is independent of the exon sequence or size and instead depends on features contained in the snRNA-like domain of the molecule. Chemical modification interference analysis has revealed that two short sequence elements in the snRNA-like domain are necessary for SL RNA activity. These elements are sufficient for such activity because when added to a 72-nucleotide fragment of a nematode U1 snRNA, this hybrid RNA could participate in trans-splicing reactions in vitro. One of the critical sequence elements may function by base-pairing with U6 snRNA, an essential U snRNA for both cis- and trans-splicing</abstract><cop>Washington, DC</cop><pub>American Society for the Advancement of Science</pub><pmid>1465612</pmid><doi>10.1126/science.1465612</doi><tpages>6</tpages></addata></record>
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source American Association for the Advancement of Science; Jstor Complete Legacy; MEDLINE
subjects Analysis
Animals
ARN
ASCARIS
Ascaris - genetics
Base Sequence
Binding Sites
Biological and medical sciences
CAENORHABDITIS ELEGANS
Exons
Fundamental and applied biological sciences. Psychology
Gels
Genetic engineering
Models, Structural
Molecular and cellular biology
Molecular genetics
Molecular Sequence Data
Molecules
Nematodes
Nucleic Acid Conformation
NUCLEOTIDE
Nucleotide sequence
Nucleotides
NUCLEOTIDOS
Purines
RNA
RNA Splicing
RNA, Messenger - genetics
RNA, Messenger - metabolism
RNA, Small Nuclear - chemistry
RNA, Small Nuclear - genetics
RNA, Small Nuclear - metabolism
Small nuclear RNA
Spliced leader RNA
Trans splicing
Transcription. Transcription factor. Splicing. Rna processing
title Interaction of U6 snRNA with a sequence required for function of the nematode SL RNA in trans-splicing
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