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Spliceosomal small nuclear ribonucleoprotein particles repeatedly cycle through Cajal bodies
D Stanek, J Pridalova-Hnilicova, I Novotny, M Huranova, M Blazikova, X Wen, AK Sapra, KM Neugebauer
Language English Country United States
NLK
Free Medical Journals
from 1992 to 2 months ago
PubMed Central
from 1992 to 2 months ago
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from 1989-11-01
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from 1997-01-01
- MeSH
- Biomarkers metabolism MeSH
- Coiled Bodies metabolism MeSH
- Financing, Organized MeSH
- HeLa Cells MeSH
- Humans MeSH
- RNA, Small Interfering metabolism MeSH
- Ribonucleoprotein, U4-U6 Small Nuclear metabolism MeSH
- Ribonucleoprotein, U5 Small Nuclear metabolism MeSH
- Survival of Motor Neuron 1 Protein metabolism MeSH
- Ribonucleoproteins, Small Nuclear metabolism MeSH
- Spliceosomes metabolism MeSH
- Carrier Proteins metabolism MeSH
- Check Tag
- Humans MeSH
The Cajal body (CB) is a nuclear structure closely associated with import and biogenesis of small nuclear ribonucleoprotein particles (snRNPs). Here, we tested whether CBs also contain mature snRNPs and whether CB integrity depends on the ongoing snRNP splicing cycle. Sm proteins tagged with photoactivatable and color-maturing variants of fluorescent proteins were used to monitor snRNP behavior in living cells over time; mature snRNPs accumulated in CBs, traveled from one CB to another, and they were not preferentially replaced by newly imported snRNPs. To test whether CB integrity depends on the snRNP splicing cycle, two human orthologues of yeast proteins involved in distinct steps in spliceosome disassembly after splicing, hPrp22 and hNtr1, were depleted by small interfering RNA treatment. Surprisingly, depletion of either protein led to the accumulation of U4/U6 snRNPs in CBs, suggesting that reassembly of the U4/U6.U5 tri-snRNP was delayed. Accordingly, a relative decrease in U5 snRNPs compared with U4/U6 snRNPs was observed in CBs, as well as in nuclear extracts of treated cells. Together, the data show that particular phases of the spliceosome cycle are compartmentalized in living cells, with reassembly of the tri-snRNP occurring in CBs.
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- $a The Cajal body (CB) is a nuclear structure closely associated with import and biogenesis of small nuclear ribonucleoprotein particles (snRNPs). Here, we tested whether CBs also contain mature snRNPs and whether CB integrity depends on the ongoing snRNP splicing cycle. Sm proteins tagged with photoactivatable and color-maturing variants of fluorescent proteins were used to monitor snRNP behavior in living cells over time; mature snRNPs accumulated in CBs, traveled from one CB to another, and they were not preferentially replaced by newly imported snRNPs. To test whether CB integrity depends on the snRNP splicing cycle, two human orthologues of yeast proteins involved in distinct steps in spliceosome disassembly after splicing, hPrp22 and hNtr1, were depleted by small interfering RNA treatment. Surprisingly, depletion of either protein led to the accumulation of U4/U6 snRNPs in CBs, suggesting that reassembly of the U4/U6.U5 tri-snRNP was delayed. Accordingly, a relative decrease in U5 snRNPs compared with U4/U6 snRNPs was observed in CBs, as well as in nuclear extracts of treated cells. Together, the data show that particular phases of the spliceosome cycle are compartmentalized in living cells, with reassembly of the tri-snRNP occurring in CBs.
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