A mutation in GRS1, a glycyl-tRNA synthetase, affects 3'-end formation in Saccharomyces cerevisiae.

3'-end formation is a complex and incompletely understood process involving both cis-acting and trans-acting factors. As part of an effort to examine the mechanisms of transcription termination by RNA polymerase II, a mutant hunt for strains defective in 3'-end formation was conducted. Following random mutagenesis, a temperature-sensitive strain exhibiting several phenotypes consistent with a role in transcription termination was isolated. First, readthrough of a terminator increases significantly in the mutant strain. Accordingly, RNA analysis indicates a decrease in the level of terminated transcripts, both in vivo and in vitro. Moreover, a plasmid stability assay in which high levels of readthrough lead to high levels of plasmid loss and transcription run-on analysis also demonstrate defective termination of transcription. Examination of polyadenylation and cleavage by the mutant strain indicates these processes are not affected. These results represent the first example of a transcription termination factor in Saccharomyces cerevisiae that affects transcription termination independent of 3'-end processing of mRNA. Complementation studies identified GRS1, an aminoacyl-tRNA synthetase, as the complementing gene. Sequence analysis of grs1-1 in the mutant strain revealed that nucleotides 1656 and 1657 were both C to T transitions, resulting in a single amino acid change of proline to phenylalanine. Further studies revealed GRS1 is essential, and the grs1-1 allele confers the temperature-sensitive growth defect associated with the mutant strain. Finally, we observed structures with some similarity to tRNA molecules within the 3'-end of various yeast genes. On the basis of our results, we suggest Grs1p is a transcription termination factor that may interact with the 3'-end of pre-mRNA to promote 3'-end formation.

[1]  H. Domdey,et al.  Mutations in a Peptidylprolyl-cis/trans-isomerase Gene Lead to a Defect in 3′-End Formation of a Pre-mRNA inSaccharomyces cerevisiae * , 1999, The Journal of Biological Chemistry.

[2]  E. Lund,et al.  Proofreading and aminoacylation of tRNAs before export from the nucleus. , 1998, Science.

[3]  H. Himeno,et al.  [A bacterial RNA that functions both as a tRNA and an mRNA]. , 1998, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

[4]  P. Schimmel,et al.  All You Need Is RNA , 1998, Science.

[5]  Michael W. Briggs,et al.  Rrp6p, the Yeast Homologue of the Human PM-Scl 100-kDa Autoantigen, Is Essential for Efficient 5.8 S rRNA 3′ End Formation* , 1998, The Journal of Biological Chemistry.

[6]  L. Minvielle-Sebastia,et al.  Coupling termination of transcription to messenger RNA maturation in yeast. , 1998, Science.

[7]  J Abelson,et al.  Evolution of a transfer RNA gene through a point mutation in the anticodon. , 1998, Science.

[8]  M. Giacca,et al.  Transcriptional interference perturbs the binding of Sp1 to the HIV-1 promoter. , 1998, Nucleic acids research.

[9]  P. Schimmel,et al.  Maintaining genetic code through adaptations of tRNA synthetases to taxonomic domains. , 1997, Trends in biochemical sciences.

[10]  J. Manley,et al.  Mechanism and regulation of mRNA polyadenylation. , 1997, Genes & development.

[11]  C. Springer,et al.  The Adjacent Yeast Genes ARO4 and HIS7Carry No Intergenic Region* , 1997, The Journal of Biological Chemistry.

[12]  L. Minvielle-Sebastia,et al.  A multisubunit 3′ end processing factor from yeast containing poly(A) polymerase and homologues of the subunits of mammalian cleavage and polyadenylation specificity factor , 1997, The EMBO journal.

[13]  L. Minvielle-Sebastia,et al.  A comparison of mammalian and yeast pre-mRNA 3'-end processing. , 1997, Current opinion in cell biology.

[14]  E J Steinmetz,et al.  Pre-mRNA Processing and the CTD of RNA Polymerase II: The Tail That Wags the Dog? , 1997, Cell.

[15]  N. Nameki,et al.  Recognition of tRNA(Gly) by three widely diverged glycyl-tRNA synthetases. , 1997, Journal of molecular biology.

[16]  J. Brune,et al.  Structural features in a brittle–ductile wax model of continental extension , 1997, nature.

[17]  C. Ball,et al.  Genetic and physical maps of Saccharomyces cerevisiae. , 1997, Nature.

[18]  M. Wickens,et al.  The C-terminal domain of RNA polymerase II couples mRNA processing to transcription , 1997, Nature.

[19]  E. Westhof,et al.  A Tyrosyl-tRNA Synthetase Recognizes a Conserved tRNA-like Structural Motif in the Group I Intron Catalytic Core , 1996, Cell.

[20]  E. Wahle,et al.  The biochemistry of polyadenylation. , 1996, Trends in biochemical sciences.

[21]  J. Butler,et al.  RNA polymerase III defects suppress a conditional-lethal poly(A) polymerase mutation in Saccharomyces cerevisiae. , 1996, Genetics.

[22]  Thomas Fiedler,et al.  A new efficient gene disruption cassette for repeated use in budding yeast , 1996, Nucleic Acids Res..

[23]  D. H. Gauss,et al.  Glycyl-tRNA synthetase. , 1996, Biological chemistry Hoppe-Seyler.

[24]  J P Sarsero,et al.  Some novel transcription attenuation mechanisms used by bacteria. , 1996, Biochimie.

[25]  D. Moras,et al.  Crystal structure of glycyl‐tRNA synthetase from Thermus thermophilus. , 1995, The EMBO journal.

[26]  P. Russo Saccharomyces cerevisiae mRNA 3′ end forming signals are also involved in transcription termination , 1995, Yeast.

[27]  T. Platt,et al.  REF2 encodes an RNA-binding protein directly involved in yeast mRNA 3'-end formation , 1995, Molecular and cellular biology.

[28]  G. Mohr,et al.  A tyrosyl-tRNA synthetase can function similarly to an RNA structure in the Tetrahymena ribozyme , 1994, Nature.

[29]  C. Moore,et al.  Termination and pausing of RNA polymerase II downstream of yeast polyadenylation sites , 1993, Molecular and cellular biology.

[30]  Gerald R. Fink,et al.  Guide to yeast genetics and molecular biology , 1993 .

[31]  N. Proudfoot,et al.  Poly(A) signals and transcriptional pause sites combine to prevent interference between RNA polymerase II promoters. , 1993, The EMBO journal.

[32]  K. Redding,et al.  An efficient procedure for multiple transformations of yeast in parallel. , 1993, BioTechniques.

[33]  C. Peebles,et al.  PTA1, an essential gene of Saccharomyces cerevisiae affecting pre-tRNA processing , 1992, Molecular and cellular biology.

[34]  C. Moore,et al.  Separation of factors required for cleavage and polyadenylation of yeast pre-mRNA , 1992, Molecular and cellular biology.

[35]  R. Schiestl,et al.  Improved method for high efficiency transformation of intact yeast cells. , 1992, Nucleic acids research.

[36]  S. Dwight,et al.  Genetic and physical maps of Saccharomyces cerevisiae. , 1997, Methods in enzymology.

[37]  R. Knippers,et al.  Binding of human glutaminyl-tRNA synthetase to a specific site of its mRNA. , 1991, Nucleic Acids Research.

[38]  C. Pleij,et al.  tRNA‐like structures , 1991 .

[39]  C. Moore,et al.  Point mutations upstream of the yeast ADH2 poly(A) site significantly reduce the efficiency of 3'-end formation , 1991, Molecular and cellular biology.

[40]  R. J. Kelleher,et al.  RNA polymerase II transcription in vitro. , 1991, Methods in enzymology.

[41]  A. Lambowitz,et al.  Involvement of aminoacyl-tRNA synthetases and other proteins in group I and group II intron splicing. , 1990, Trends in biochemical sciences.

[42]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[43]  V. Walbot,et al.  RNA pseudoknot domain of tobacco mosaic virus can functionally substitute for a poly(A) tail in plant and animal cells. , 1990, Genes & development.

[44]  F. Sherman,et al.  Transcription terminates near the poly(A) site in the CYC1 gene of the yeast Saccharomyces cerevisiae. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[45]  J. Butler,et al.  RNA processing generates the mature 3' end of yeast CYC1 messenger RNA in vitro. , 1988, Science.

[46]  R. W. Davis,et al.  Transcription interferes with elements important for chromosome maintenance in Saccharomyces cerevisiae , 1988, Molecular and cellular biology.

[47]  R. Kornberg,et al.  Accurate initiation at RNA polymerase II promoters in extracts from Saccharomyces cerevisiae. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[48]  D. Botstein,et al.  A Saccharomyces cerevisiae genomic plasmid bank based on a centromere-containing shuttle vector. , 1987, Gene.

[49]  N. Proudfoot,et al.  Alpha‐thalassaemia caused by a poly(A) site mutation reveals that transcriptional termination is linked to 3′ end processing in the human alpha 2 globin gene. , 1986, The EMBO journal.

[50]  N. Proudfoot Transcriptional interference and termination between duplicated α-globin gene constructs suggests a novel mechanism for gene regulation , 1986, Nature.

[51]  G. Fink,et al.  Laboratory course manual for methods in yeast genetics , 1986 .

[52]  Ronald W. Davis,et al.  Mitotic stability of yeast chromosomes: A colony color assay that measures nondisjunction and chromosome loss , 1985, Cell.

[53]  L. Hartwell,et al.  Genetic analysis of the mitotic transmission of minichromosomes , 1985, Cell.

[54]  R. W. Davis,et al.  Sequences that regulate the divergent GAL1-GAL10 promoter in Saccharomyces cerevisiae , 1984, Molecular and cellular biology.

[55]  F. Sherman,et al.  DNA sequence required for efficient transcription termination in yeast , 1982, Cell.