Pseudouridylation of yeast U2 snRNA is catalyzed by either an RNA-guided or RNA-independent mechanism

Yeast U2 small nuclear RNA (snRNA) contains three pseudouridines (Ψ35, Ψ42, and Ψ44). Pus7p and Pus1p catalyze the formation of Ψ35 and Ψ44, respectively, but the mechanism of Ψ42 formation remains unclear. Using a U2 substrate containing a single 32 P radiolabel at position 42, we screened a GST‐OR...

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Veröffentlicht in:The EMBO journal 2005-07, Vol.24 (13), p.2403-2413
Hauptverfasser: Ma, X, Yang, C, Alexandrov, A, Grayhack, E.J, Behm-Ansmant, I, Yu, Y.T
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creator Ma, X
Yang, C
Alexandrov, A
Grayhack, E.J
Behm-Ansmant, I
Yu, Y.T
description Yeast U2 small nuclear RNA (snRNA) contains three pseudouridines (Ψ35, Ψ42, and Ψ44). Pus7p and Pus1p catalyze the formation of Ψ35 and Ψ44, respectively, but the mechanism of Ψ42 formation remains unclear. Using a U2 substrate containing a single 32 P radiolabel at position 42, we screened a GST‐ORF library for pseudouridylase activity. Surprisingly, we found a Ψ42‐specific pseudouridylase activity that coincided with Nhp2p, a protein component of a Box H/ACA sno/scaRNP (small nucleolar/Cajal body‐specific ribonucleoprotein). When isolated by tandem affinity purification (TAP), the other protein components of the H/ACA sno/scaRNP also copurified with the pseudouridylase activity. Micrococcal nuclease‐treated TAP preparations were devoid of pseudouridylase activity; however, activity was restored upon addition of RNAs from TAP preparations. Pseudouridylation reconstitution using RNAs from a Box H/ACA RNA library identified snR81, a snoRNA known to guide rRNA pseudouridylation, as the Ψ42‐specific guide RNA. Using the snR81‐deletion strain, Nhp2p‐ or Cbf5p‐conditional depletion strain, and a cbf5 mutation strain, we further demonstrated that the pseudouridylase activity is dependent on snR81 snoRNP in vivo . Our data indicate that snRNA pseudouridylation can be catalyzed by both RNA‐dependent and RNA‐independent mechanisms.
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Pus7p and Pus1p catalyze the formation of Ψ35 and Ψ44, respectively, but the mechanism of Ψ42 formation remains unclear. Using a U2 substrate containing a single 32 P radiolabel at position 42, we screened a GST‐ORF library for pseudouridylase activity. Surprisingly, we found a Ψ42‐specific pseudouridylase activity that coincided with Nhp2p, a protein component of a Box H/ACA sno/scaRNP (small nucleolar/Cajal body‐specific ribonucleoprotein). When isolated by tandem affinity purification (TAP), the other protein components of the H/ACA sno/scaRNP also copurified with the pseudouridylase activity. Micrococcal nuclease‐treated TAP preparations were devoid of pseudouridylase activity; however, activity was restored upon addition of RNAs from TAP preparations. Pseudouridylation reconstitution using RNAs from a Box H/ACA RNA library identified snR81, a snoRNA known to guide rRNA pseudouridylation, as the Ψ42‐specific guide RNA. Using the snR81‐deletion strain, Nhp2p‐ or Cbf5p‐conditional depletion strain, and a cbf5 mutation strain, we further demonstrated that the pseudouridylase activity is dependent on snR81 snoRNP in vivo . 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Pus7p and Pus1p catalyze the formation of Ψ35 and Ψ44, respectively, but the mechanism of Ψ42 formation remains unclear. Using a U2 substrate containing a single 32 P radiolabel at position 42, we screened a GST‐ORF library for pseudouridylase activity. Surprisingly, we found a Ψ42‐specific pseudouridylase activity that coincided with Nhp2p, a protein component of a Box H/ACA sno/scaRNP (small nucleolar/Cajal body‐specific ribonucleoprotein). When isolated by tandem affinity purification (TAP), the other protein components of the H/ACA sno/scaRNP also copurified with the pseudouridylase activity. Micrococcal nuclease‐treated TAP preparations were devoid of pseudouridylase activity; however, activity was restored upon addition of RNAs from TAP preparations. Pseudouridylation reconstitution using RNAs from a Box H/ACA RNA library identified snR81, a snoRNA known to guide rRNA pseudouridylation, as the Ψ42‐specific guide RNA. 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Pus7p and Pus1p catalyze the formation of Ψ35 and Ψ44, respectively, but the mechanism of Ψ42 formation remains unclear. Using a U2 substrate containing a single 32 P radiolabel at position 42, we screened a GST‐ORF library for pseudouridylase activity. Surprisingly, we found a Ψ42‐specific pseudouridylase activity that coincided with Nhp2p, a protein component of a Box H/ACA sno/scaRNP (small nucleolar/Cajal body‐specific ribonucleoprotein). When isolated by tandem affinity purification (TAP), the other protein components of the H/ACA sno/scaRNP also copurified with the pseudouridylase activity. Micrococcal nuclease‐treated TAP preparations were devoid of pseudouridylase activity; however, activity was restored upon addition of RNAs from TAP preparations. Pseudouridylation reconstitution using RNAs from a Box H/ACA RNA library identified snR81, a snoRNA known to guide rRNA pseudouridylation, as the Ψ42‐specific guide RNA. 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subjects Catalysis
EMBO36
Gene Library
Hydro-Lyases - metabolism
Microtubule-Associated Proteins - metabolism
Mutation
Nuclear Proteins - metabolism
pseudouridine
Pseudouridine - metabolism
pseudouridylase
pseudouridylation
pseudouridylation reconstitution
Ribonucleoproteins, Small Nuclear - metabolism
Ribonucleoproteins, Small Nucleolar - metabolism
ribonucleosides
RNA pseudouridylation
RNA, Fungal - metabolism
RNA, Small Nuclear - chemistry
RNA, Small Nuclear - metabolism
RNA, Small Nucleolar - metabolism
S. cerevisiae
Saccharomyces cerevisiae
Saccharomyces cerevisiae - metabolism
Saccharomyces cerevisiae Proteins - metabolism
small nuclear RNA
snR81 snoRNP
U2 snRNA
Yeasts
title Pseudouridylation of yeast U2 snRNA is catalyzed by either an RNA-guided or RNA-independent mechanism
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