Abstract
In order to identify catalytically important amino acid changes within the second-largest subunit of yeast RNA polymerase III, we mutagenized selected regions of its gene (RET1) and devised in vivo assays for both increased and decreased transcription termination by this enzyme. Using as the reporter gene a mutant SUP4-o tRNA gene that in one case terminates prematurely and in the other case fails to terminate, we screened mutagenized RET1 libraries for reduced and increased transcription termination, respectively. The gain in suppression phenotype was in both cases scored as a reduction in the accumulation of red pigment in yeast strains harboring the ade2-1 ochre mutation. Termination-altering mutations were obtained in regions of the RET1 gene encoding amino acids 300 to 325, 455 to 486, 487 to 521, and 1061 to 1082 of the protein. In degree of amino acid sequence conservation, these range from highly variable in the first to highly conserved in the last two regions. Residues 300 to 325 yielded mainly reduced-termination mutants, while in region 1061 to 1082, increased-termination mutants were obtained exclusively. All mutants recovered, while causing gain of suppression with one SUP4 allele, brought about a reduction in suppression with the other allele, thus confirming that the phenotype is due to altered termination rather than an elevated level of transcription initiation. In vitro transcription reactions performed with extracts from several strong mutants demonstrated that the mutant polymerases respond to RNA terminator sequences in a manner that matches their in vivo termination phenotypes.
Full Text
The Full Text of this article is available as a PDF (471.3 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Allison D. S., Goh S. H., Hall B. D. The promoter sequence of a yeast tRNAtyr gene. Cell. 1983 Sep;34(2):655–664. doi: 10.1016/0092-8674(83)90398-7. [DOI] [PubMed] [Google Scholar]
- Allison D. S., Hall B. D. Effects of alterations in the 3' flanking sequence on in vivo and in vitro expression of the yeast SUP4-o tRNATyr gene. EMBO J. 1985 Oct;4(10):2657–2664. doi: 10.1002/j.1460-2075.1985.tb03984.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Arndt K. M., Chamberlin M. J. RNA chain elongation by Escherichia coli RNA polymerase. Factors affecting the stability of elongating ternary complexes. J Mol Biol. 1990 May 5;213(1):79–108. doi: 10.1016/S0022-2836(05)80123-8. [DOI] [PubMed] [Google Scholar]
- Baker R. E., Hall B. D. Structural features of yeast tRNA genes which affect transcription factor binding. EMBO J. 1984 Dec 1;3(12):2793–2800. doi: 10.1002/j.1460-2075.1984.tb02211.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benner S. A., Gerloff D. Patterns of divergence in homologous proteins as indicators of secondary and tertiary structure: a prediction of the structure of the catalytic domain of protein kinases. Adv Enzyme Regul. 1991;31:121–181. doi: 10.1016/0065-2571(91)90012-b. [DOI] [PubMed] [Google Scholar]
- Bogenhagen D. F., Brown D. D. Nucleotide sequences in Xenopus 5S DNA required for transcription termination. Cell. 1981 Apr;24(1):261–270. doi: 10.1016/0092-8674(81)90522-5. [DOI] [PubMed] [Google Scholar]
- Bonner G., Patra D., Lafer E. M., Sousa R. Mutations in T7 RNA polymerase that support the proposal for a common polymerase active site structure. EMBO J. 1992 Oct;11(10):3767–3775. doi: 10.1002/j.1460-2075.1992.tb05462.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Braus G., Furter R., Prantl F., Niederberger P., Hütter R. Arrangement of genes TRP1 and TRP3 of Saccharomyces cerevisiae strains. Arch Microbiol. 1985 Sep;142(4):383–388. doi: 10.1007/BF00491908. [DOI] [PubMed] [Google Scholar]
- Campbell F. E., Jr, Setzer D. R. Transcription termination by RNA polymerase III: uncoupling of polymerase release from termination signal recognition. Mol Cell Biol. 1992 May;12(5):2260–2272. doi: 10.1128/mcb.12.5.2260. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Connelly S., Manley J. L. A functional mRNA polyadenylation signal is required for transcription termination by RNA polymerase II. Genes Dev. 1988 Apr;2(4):440–452. doi: 10.1101/gad.2.4.440. [DOI] [PubMed] [Google Scholar]
- Cozzarelli N. R., Gerrard S. P., Schlissel M., Brown D. D., Bogenhagen D. F. Purified RNA polymerase III accurately and efficiently terminates transcription of 5S RNA genes. Cell. 1983 Oct;34(3):829–835. doi: 10.1016/0092-8674(83)90540-8. [DOI] [PubMed] [Google Scholar]
- Eggermont J., Proudfoot N. J. Poly(A) signals and transcriptional pause sites combine to prevent interference between RNA polymerase II promoters. EMBO J. 1993 Jun;12(6):2539–2548. doi: 10.1002/j.1460-2075.1993.tb05909.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Enriquez-Harris P., Levitt N., Briggs D., Proudfoot N. J. A pause site for RNA polymerase II is associated with termination of transcription. EMBO J. 1991 Jul;10(7):1833–1842. doi: 10.1002/j.1460-2075.1991.tb07709.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grachev M. A., Kolocheva T. I., Lukhtanov E. A., Mustaev A. A. Studies on the functional topography of Escherichia coli RNA polymerase. Highly selective affinity labelling by analogues of initiating substrates. Eur J Biochem. 1987 Feb 16;163(1):113–121. doi: 10.1111/j.1432-1033.1987.tb10743.x. [DOI] [PubMed] [Google Scholar]
- Grachev M. A., Lukhtanov E. A., Mustaev A. A., Zaychikov E. F., Abdukayumov M. N., Rabinov I. V., Richter V. I., Skoblov Y. S., Chistyakov P. G. Studies of the functional topography of Escherichia coli RNA polymerase. A method for localization of the sites of affinity labelling. Eur J Biochem. 1989 Apr 1;180(3):577–585. doi: 10.1111/j.1432-1033.1989.tb14684.x. [DOI] [PubMed] [Google Scholar]
- Hermes J. D., Blacklow S. C., Knowles J. R. Searching sequence space by definably random mutagenesis: improving the catalytic potency of an enzyme. Proc Natl Acad Sci U S A. 1990 Jan;87(2):696–700. doi: 10.1073/pnas.87.2.696. [DOI] [PMC free article] [PubMed] [Google Scholar]
- James P., Hall B. D. ret1-1, a yeast mutant affecting transcription termination by RNA polymerase III. Genetics. 1990 Jun;125(2):293–303. doi: 10.1093/genetics/125.2.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
- James P., Whelen S., Hall B. D. The RET1 gene of yeast encodes the second-largest subunit of RNA polymerase III. Structural analysis of the wild-type and ret1-1 mutant alleles. J Biol Chem. 1991 Mar 25;266(9):5616–5624. [PubMed] [Google Scholar]
- Jin D. J., Gross C. A. Mapping and sequencing of mutations in the Escherichia coli rpoB gene that lead to rifampicin resistance. J Mol Biol. 1988 Jul 5;202(1):45–58. doi: 10.1016/0022-2836(88)90517-7. [DOI] [PubMed] [Google Scholar]
- Jin D. J., Gross C. A. RpoB8, a rifampicin-resistant termination-proficient RNA polymerase, has an increased Km for purine nucleotides during transcription elongation. J Biol Chem. 1991 Aug 5;266(22):14478–14485. [PubMed] [Google Scholar]
- Jin D. J., Walter W. A., Gross C. A. Characterization of the termination phenotypes of rifampicin-resistant mutants. J Mol Biol. 1988 Jul 20;202(2):245–253. doi: 10.1016/0022-2836(88)90455-x. [DOI] [PubMed] [Google Scholar]
- Ju Q. D., Morrow B. E., Warner J. R. REB1, a yeast DNA-binding protein with many targets, is essential for growth and bears some resemblance to the oncogene myb. Mol Cell Biol. 1990 Oct;10(10):5226–5234. doi: 10.1128/mcb.10.10.5226. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kashlev M. V., Bass I. A., Lebedev A. N., Kaliaeva E. S., Nikiforov V. G. Deletsionno-insertsionnoe kartirovanie oblasti, ne sushchestvennoi dlia funktsionirovaniia beta-sub"edinitsy RNK-polimerazy Escherichia coli. Genetika. 1989 Mar;25(3):396–405. [PubMed] [Google Scholar]
- Kashlev M., Nudler E., Goldfarb A., White T., Kutter E. Bacteriophage T4 Alc protein: a transcription termination factor sensing local modification of DNA. Cell. 1993 Oct 8;75(1):147–154. [PubMed] [Google Scholar]
- Kolodziej P. A., Young R. A. Mutations in the three largest subunits of yeast RNA polymerase II that affect enzyme assembly. Mol Cell Biol. 1991 Sep;11(9):4669–4678. doi: 10.1128/mcb.11.9.4669. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kuhn A., Bartsch I., Grummt I. Specific interaction of the murine transcription termination factor TTF I with class-I RNA polymerases. Nature. 1990 Apr 5;344(6266):559–562. doi: 10.1038/344559a0. [DOI] [PubMed] [Google Scholar]
- Landick R., Stewart J., Lee D. N. Amino acid changes in conserved regions of the beta-subunit of Escherichia coli RNA polymerase alter transcription pausing and termination. Genes Dev. 1990 Sep;4(9):1623–1636. doi: 10.1101/gad.4.9.1623. [DOI] [PubMed] [Google Scholar]
- Lang W. H., Reeder R. H. The REB1 site is an essential component of a terminator for RNA polymerase I in Saccharomyces cerevisiae. Mol Cell Biol. 1993 Jan;13(1):649–658. doi: 10.1128/mcb.13.1.649. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lau L. F., Roberts J. W., Wu R. RNA polymerase pausing and transcript release at the lambda tR1 terminator in vitro. J Biol Chem. 1983 Aug 10;258(15):9391–9397. [PubMed] [Google Scholar]
- Manley J. L., Proudfoot N. J., Platt T. RNA 3'-end formation. Genes Dev. 1989 Dec;3(12B):2218–2222. doi: 10.1101/gad.3.12b.2218. [DOI] [PubMed] [Google Scholar]
- Mann C., Buhler J. M., Treich I., Sentenac A. RPC40, a unique gene for a subunit shared between yeast RNA polymerases A and C. Cell. 1987 Feb 27;48(4):627–637. doi: 10.1016/0092-8674(87)90241-8. [DOI] [PubMed] [Google Scholar]
- Martin C., Okamura S., Young R. Genetic exploration of interactive domains in RNA polymerase II subunits. Mol Cell Biol. 1990 May;10(5):1908–1914. doi: 10.1128/mcb.10.5.1908. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mazabraud A., Scherly D., Müller F., Rungger D., Clarkson S. G. Structure and transcription termination of a lysine tRNA gene from Xenopus laevis. J Mol Biol. 1987 Jun 20;195(4):835–845. doi: 10.1016/0022-2836(87)90488-8. [DOI] [PubMed] [Google Scholar]
- Morgan W. D., Bear D. G., von Hippel P. H. Rho-dependent termination of transcription. II. Kinetics of mRNA elongation during transcription from the bacteriophage lambda PR promoter. J Biol Chem. 1983 Aug 10;258(15):9565–9574. [PubMed] [Google Scholar]
- Mustaev A., Kashlev M., Lee J. Y., Polyakov A., Lebedev A., Zalenskaya K., Grachev M., Goldfarb A., Nikiforov V. Mapping of the priming substrate contacts in the active center of Escherichia coli RNA polymerase. J Biol Chem. 1991 Dec 15;266(35):23927–23931. [PubMed] [Google Scholar]
- Nakamaye K. L., Eckstein F. Inhibition of restriction endonuclease Nci I cleavage by phosphorothioate groups and its application to oligonucleotide-directed mutagenesis. Nucleic Acids Res. 1986 Dec 22;14(24):9679–9698. doi: 10.1093/nar/14.24.9679. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Osumi-Davis P. A., de Aguilera M. C., Woody R. W., Woody A. Y. Asp537, Asp812 are essential and Lys631, His811 are catalytically significant in bacteriophage T7 RNA polymerase activity. J Mol Biol. 1992 Jul 5;226(1):37–45. doi: 10.1016/0022-2836(92)90122-z. [DOI] [PubMed] [Google Scholar]
- Pelletier H., Sawaya M. R., Kumar A., Wilson S. H., Kraut J. Structures of ternary complexes of rat DNA polymerase beta, a DNA template-primer, and ddCTP. Science. 1994 Jun 24;264(5167):1891–1903. [PubMed] [Google Scholar]
- Polesky A. H., Dahlberg M. E., Benkovic S. J., Grindley N. D., Joyce C. M. Side chains involved in catalysis of the polymerase reaction of DNA polymerase I from Escherichia coli. J Biol Chem. 1992 Apr 25;267(12):8417–8428. [PubMed] [Google Scholar]
- Riva M., Schäffner A. R., Sentenac A., Hartmann G. R., Mustaev A. A., Zaychikov E. F., Grachev M. A. Active site labeling of the RNA polymerases A, B, and C from yeast. J Biol Chem. 1987 Oct 25;262(30):14377–14380. [PubMed] [Google Scholar]
- Ruteshouser E. C., Richardson J. P. Identification and characterization of transcription termination sites in the Escherichia coli lacZ gene. J Mol Biol. 1989 Jul 5;208(1):23–43. doi: 10.1016/0022-2836(89)90085-5. [DOI] [PubMed] [Google Scholar]
- Sawaya M. R., Pelletier H., Kumar A., Wilson S. H., Kraut J. Crystal structure of rat DNA polymerase beta: evidence for a common polymerase mechanism. Science. 1994 Jun 24;264(5167):1930–1935. doi: 10.1126/science.7516581. [DOI] [PubMed] [Google Scholar]
- Schulz W., Zillig W. Rifampicin inhibition of RNA synthesis by destabilisation of DNA-RNA polymerase-oligonucleotide-complexes. Nucleic Acids Res. 1981 Dec 21;9(24):6889–6906. doi: 10.1093/nar/9.24.6889. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Severinov K., Kashlev M., Severinova E., Bass I., McWilliams K., Kutter E., Nikiforov V., Snyder L., Goldfarb A. A non-essential domain of Escherichia coli RNA polymerase required for the action of the termination factor Alc. J Biol Chem. 1994 May 13;269(19):14254–14259. [PubMed] [Google Scholar]
- Sikorski R. S., Hieter P. A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae. Genetics. 1989 May;122(1):19–27. doi: 10.1093/genetics/122.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smid A., Finsterer M., Grummt I. Limited proteolysis unmasks specific DNA-binding of the murine RNA polymerase I-specific transcription termination factor TTFI. J Mol Biol. 1992 Oct 5;227(3):635–647. doi: 10.1016/0022-2836(92)90213-4. [DOI] [PubMed] [Google Scholar]
- Suzuki M. SPXX, a frequent sequence motif in gene regulatory proteins. J Mol Biol. 1989 May 5;207(1):61–84. doi: 10.1016/0022-2836(89)90441-5. [DOI] [PubMed] [Google Scholar]
- Sweetser D., Nonet M., Young R. A. Prokaryotic and eukaryotic RNA polymerases have homologous core subunits. Proc Natl Acad Sci U S A. 1987 Mar;84(5):1192–1196. doi: 10.1073/pnas.84.5.1192. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vieira J., Messing J. Production of single-stranded plasmid DNA. Methods Enzymol. 1987;153:3–11. doi: 10.1016/0076-6879(87)53044-0. [DOI] [PubMed] [Google Scholar]
- Watson J. B., Chandler D. W., Gralla J. D. Specific termination of in vitro transcription by calf thymus RNA polymerase III. Nucleic Acids Res. 1984 Jul 11;12(13):5369–5384. doi: 10.1093/nar/12.13.5369. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yager T. D., von Hippel P. H. A thermodynamic analysis of RNA transcript elongation and termination in Escherichia coli. Biochemistry. 1991 Jan 29;30(4):1097–1118. doi: 10.1021/bi00218a032. [DOI] [PubMed] [Google Scholar]
- von Hippel P. H., Yager T. D. Transcript elongation and termination are competitive kinetic processes. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2307–2311. doi: 10.1073/pnas.88.6.2307. [DOI] [PMC free article] [PubMed] [Google Scholar]