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PMID: 7515008 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

The 5' end of yeast 5.8S rRNA is generated by exonucleases from an upstream cleavage site.

The EMBO journal ·Vol. 13 ·No. 10 ·1994-05-15 ·Pages 2452-63

Henry Y, Wood H, Morrissey JP, Petfalski E, Kearsey S, Tollervey D

Abstract

We have developed techniques for the detailed analysis of cis-acting sequences in the pre-rRNA of Saccharomyces cerevisiae and used these to study the processing of internal transcribed spacer 1 (ITS1) leading to the synthesis of 5.8S rRNA. As is the case for many eukaryotes, the 5' end of yeast 5.8S rRNA is heterogeneous; we designate the major, short form 5.8S(S), and the minor form (which is seven or eight nucleotides longer) 5.8S(L). These RNAs do not have a precursor/product relationship, but result from the use of alternative processing pathways. In the major pathway, a previously unidentified processing site in ITS1, designated A3, is cleaved. A 10 nucleotide deletion at site A3 strongly inhibits processing of A3 and the synthesis of 5.8S(S); processing is predominantly transferred to the alternative 5.8S(L) pathway. Site A3 lies 76 nucleotides 5' to the end of 5.8S(S), and acts as an entry site for 5'-->3' exonuclease digestion which generates the 5' end of 5.8S(S). This pathway is inhibited in strains mutant for XRN1p and RAT1p. Both of these proteins have been reported to have 5'-->3' exonuclease activity in vitro. Formation of 5.8S(L) is increased by mutations at A3 in cis or in RAT1p and XRN1p in trans, and is kinetically faster than 5.8S(S) synthesis.

MeSH Terms
Base Sequence DNA Mutational Analysis DNA, Ribosomal/genetics Exonucleases/metabolism Genetic Variation Molecular Sequence Data RNA/biosynthesis RNA Precursors/genetics,metabolism RNA Processing, Post-Transcriptional RNA, Ribosomal, 5.8S/biosynthesis,genetics Regulatory Sequences, Nucleic Acid/genetics Saccharomyces cerevisiae/genetics Sequence Deletion
Chemicals
DNA, Ribosomal RNA Precursors RNA, Ribosomal, 5.8S RNA, recombinant RNA Exonucleases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Henry Y
EMBL, Heidelberg, Germany.
Wood H
Morrissey J P
Petfalski E
Kearsey S
Tollervey D
References (44)
44 references, click to expand
  1. A temperature sensitive mutant of Saccharomyces cerevisiae defective in pre-rRNA processing.
    Nucleic Acids Res. 1991 Sep 25;19(18):5059-64 PMID: 1923772
  2. Rat nucleolar 7-2 RNA is homologous to mouse mitochondrial RNase mitochondrial RNA-processing RNA.
    J Biol Chem. 1989 Sep 5;264(25):14835-9 PMID: 2475491
  3. Functional analysis of transcribed spacers of yeast ribosomal DNA.
    EMBO J. 1990 Dec;9(12):3989-96 PMID: 2249660
  4. Antisense oligonucleotides made of 2'-O-alkylRNA: their properties and applications in RNA biochemistry.
    FEBS Lett. 1993 Jun 28;325(1-2):123-7 PMID: 7685712
  5. Depletion of U14 small nuclear RNA (snR128) disrupts production of 18S rRNA in Saccharomyces cerevisiae.
    Mol Cell Biol. 1990 Mar;10(3):1145-52 PMID: 2406561
  6. Depletion of U3 small nucleolar RNA inhibits cleavage in the 5' external transcribed spacer of yeast pre-ribosomal RNA and impairs formation of 18S ribosomal RNA.
    EMBO J. 1991 Dec;10(13):4231-9 PMID: 1756730
  7. Saccharomyces cerevisiae contains an RNase MRP that cleaves at a conserved mitochondrial RNA sequence implicated in replication priming.
    Mol Cell Biol. 1992 Jun;12(6):2561-9 PMID: 1588958
  8. A U3 snoRNP protein with homology to splicing factor PRP4 and G beta domains is required for ribosomal RNA processing.
    EMBO J. 1993 Jun;12(6):2549-58 PMID: 8508778
  9. The RNA of RNase MRP is required for normal processing of ribosomal RNA.
    Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):659-63 PMID: 8290578
  10. The nucleotide sequence of the intergenic region between the 5.8S and 26S rRNA genes of the yeast ribosomal RNA operon. Possible implications for the interaction between 5.8S and 26S rRNA and the processing of the primary transcript.
    Nucleic Acids Res. 1981 Oct 10;9(19):4847-62 PMID: 7312619
  11. Secondary methylation of yeast ribosomal precursor RNA.
    Eur J Biochem. 1977 May 2;75(1):311-8 PMID: 405217
  12. An essential yeast gene with homology to the exonuclease-encoding XRN1/KEM1 gene also encodes a protein with exoribonuclease activity.
    Mol Cell Biol. 1993 Jan;13(1):341-50 PMID: 8417335
  13. Fragments of the internal transcribed spacer 1 of pre-rRNA accumulate in Saccharomyces cerevisiae lacking 5'----3' exoribonuclease 1.
    J Bacteriol. 1991 Nov;173(21):7024-8 PMID: 1938905
  14. Identification and functional analysis of two U3 binding sites on yeast pre-ribosomal RNA.
    EMBO J. 1992 Apr;11(4):1531-42 PMID: 1563354
  15. Purification and characterization of a Saccharomyces cerevisiae exoribonuclease which yields 5'-mononucleotides by a 5' leads to 3' mode of hydrolysis.
    J Biol Chem. 1980 Apr 10;255(7):3080-5 PMID: 6244307
  16. A novel endoribonuclease cleaves at a priming site of mouse mitochondrial DNA replication.
    EMBO J. 1987 Feb;6(2):409-17 PMID: 3582365
  17. GAR1 is an essential small nucleolar RNP protein required for pre-rRNA processing in yeast.
    EMBO J. 1992 Feb;11(2):673-82 PMID: 1531632
  18. Nuclear RNase MRP is required for correct processing of pre-5.8S rRNA in Saccharomyces cerevisiae.
    Mol Cell Biol. 1993 Dec;13(12):7935-41 PMID: 8247008
  19. Functional analysis of internal transcribed spacer 2 of Saccharomyces cerevisiae ribosomal DNA.
    J Mol Biol. 1992 Feb 20;223(4):899-910 PMID: 1538404
  20. rar mutations which increase artificial chromosome stability in Saccharomyces cerevisiae identify transcription and recombination proteins.
    Nucleic Acids Res. 1991 Apr 11;19(7):1385-91 PMID: 2027746
  21. A system for the analysis of yeast ribosomal DNA mutations.
    Mol Cell Biol. 1989 Feb;9(2):551-9 PMID: 2540422
  22. Antisense probes containing 2-aminoadenosine allow efficient depletion of U5 snRNP from HeLa splicing extracts.
    Nucleic Acids Res. 1991 Jun 25;19(12):3193-8 PMID: 1648201
  23. A mammalian mitochondrial RNA processing activity contains nucleus-encoded RNA.
    Science. 1987 Mar 6;235(4793):1178-84 PMID: 2434997
  24. Ribosomal RNA synthesis in Saccharomyces cerevisiae.
    J Mol Biol. 1972 Mar 28;65(2):227-42 PMID: 4557192
  25. Internal transcribed spacer 1 of the yeast precursor ribosomal RNA. Higher order structure and common structural motifs.
    Biochemistry. 1990 Jun 26;29(25):5911-8 PMID: 2116901
  26. Isolation and characterization of yeast ribosomal RNA precursors and preribosomes.
    Methods Enzymol. 1989;180:96-109 PMID: 2693913
  27. Recombination and RNA processing: a common strand?
    Trends Cell Biol. 1991 Nov;1(5):110-2 PMID: 14731541
  28. Some characteristics of processing sites in ribosomal precursor RNA of yeast.
    Nucleic Acids Res. 1980 Jul 11;8(13):2907-20 PMID: 6253896
  29. Synthesis of large rRNAs by RNA polymerase II in mutants of Saccharomyces cerevisiae defective in RNA polymerase I.
    Proc Natl Acad Sci U S A. 1991 May 1;88(9):3962-6 PMID: 2023944
  30. Yeast site-specific ribonucleoprotein endoribonuclease MRP contains an RNA component homologous to mammalian RNase MRP RNA and essential for cell viability.
    Genes Dev. 1992 Oct;6(10):1975-85 PMID: 1398074
  31. Fungal small nuclear ribonucleoproteins share properties with plant and vertebrate U-snRNPs.
    EMBO J. 1987 Feb;6(2):469-76 PMID: 2953599
  32. A new rRNA processing mutant of Saccharomyces cerevisiae.
    Nucleic Acids Res. 1992 Jan 25;20(2):295-301 PMID: 1741255
  33. Structure of the yeast TAP1 protein: dependence of transcription activation on the DNA context of the target gene.
    Mol Cell Biol. 1993 Jun;13(6):3434-44 PMID: 8497260
  34. Characterization of the XRN1 gene encoding a 5'-->3' exoribonuclease: sequence data and analysis of disparate protein and mRNA levels of gene-disrupted yeast cells.
    Gene. 1992 Oct 12;120(1):51-7 PMID: 1398123
  35. Primary and secondary structure of U8 small nuclear RNA.
    J Biol Chem. 1985 Sep 15;260(20):10930-5 PMID: 2411727
  36. The numerous modified nucleotides in eukaryotic ribosomal RNA.
    Prog Nucleic Acid Res Mol Biol. 1990;39:241-303 PMID: 2247610
  37. Isolation and characterization of temperature-sensitive mutations in RPA190, the gene encoding the largest subunit of RNA polymerase I from Saccharomyces cerevisiae.
    Mol Cell Biol. 1988 Oct;8(10):3997-4008 PMID: 3054507
  38. 7-2/MRP RNAs in plant and mammalian cells: association with higher order structures in the nucleolus.
    EMBO J. 1992 Oct;11(10):3737-46 PMID: 1382978
  39. The small nucleolar RNP protein NOP1 (fibrillarin) is required for pre-rRNA processing in yeast.
    EMBO J. 1991 Mar;10(3):573-83 PMID: 1825809
  40. Gene RRN4 in Saccharomyces cerevisiae encodes the A12.2 subunit of RNA polymerase I and is essential only at high temperatures.
    Mol Cell Biol. 1993 Jan;13(1):114-22 PMID: 8417319
  41. TAP1, a yeast gene that activates the expression of a tRNA gene with a defective internal promoter.
    Mol Cell Biol. 1993 Jun;13(6):3424-33 PMID: 8497259
  42. Characterization and subcellular localization of 7-8 S RNAs of Novikoff hepatoma.
    J Biol Chem. 1981 Aug 25;256(16):8452-7 PMID: 6167578
  43. Yeast cells lacking 5'-->3' exoribonuclease 1 contain mRNA species that are poly(A) deficient and partially lack the 5' cap structure.
    Mol Cell Biol. 1993 Aug;13(8):4826-35 PMID: 8336719
  44. Yeast snR30 is a small nucleolar RNA required for 18S rRNA synthesis.
    Mol Cell Biol. 1993 Apr;13(4):2469-77 PMID: 8455623
Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
1994-05-15
Pages
2452-63
Language
English
Region
England
NLM ID
8208664
PMCID
PMC395111
Subset
IM
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