5
Views
9
CrossRef citations to date
0
Altmetric
Gene Expression

Signals That Produce 3′ Termini in CYC1 mRNA of the Yeast Saccharomyces cerevisiae

, , &
Pages 7836-7849 | Received 11 Jun 1993, Accepted 16 Sep 1993, Published online: 31 Mar 2023

References

  • Boss, J. M., S. Gillam, R. S. Zitomer, and M. Smith. 1981. Sequence of the yeast iso-1-cytochrome c mRNA. J. Biol. Chem. 256:12958–12961.
  • Butler, J. S., and T. Platt. 1988. RNA processing generates the mature 3′ end of yeast CYC1 messenger RNA in vitro. Science 242:1270–1274.
  • Cardillo, T. Unpublished data.
  • Ceseareni, G. Unpublished data.
  • Fitzgerald, M., and T. Shenk. 1981. The sequence 5′-AAUAAA-3′ forms part of the recognition site for polyadenyl-ation of late SV40 mRNAs. Cell 24:251–260.
  • Heidmann, S., B. Obermaier, K. Vogel, and H. Domdey. 1992. Identification of pre-mRNA polyadenylation sites in Saccharomyces cerevisiae. Mol. Cell. Biol. 12:4215–4229.
  • Henikoff, S., and E. H. Cohen. 1984. Sequences responsible for transcription termination on a gene segment in Saccharomyces cerevisiae. Mol. Cell. Biol. 4:1515–1520.
  • Hyman, L. A., S. H. Seiler, J. Whoiskey, and C. L. Moore. 1991. Point mutations upstream of the yeast ADH2 poly(A) site significantly reduce the efficiency of 3′ end formation. Mol. Cell. Biol. 11:2004–2012.
  • Irniger, S., C. M. Egli, and G. Braus. 1991. Different classes of polyadenylation sites in the yeast Saccharomyces cerevisiae. Mol. Cell. Biol. 11:3060–3069.
  • Irniger, S., H. Sanfaçon, C. M. Egli, and G. H. Braus. 1992. Different sequence elements are required for function of the cauliflower mosaic virus polyadenylation site in Saccharomyces cerevisiae compared to plants. Mol. Cell. Biol. 12:2322–2330.
  • Kunkel, T. A., J. D. Roberts, and R. A. Zakoar. 1987. Rapid and efficient site-specific mutagenesis without phenotypic selection. Methods Enzymol. 154:367–382.
  • Maxam, A. M., and W. Gilbert. 1980. Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol. 65:499–559.
  • Osborn, B. I., and L. Guarente. 1989. Mutational analysis of a yeast transcriptional terminator. Proc. Natl. Acad. Sci. USA 86:4097–4101.
  • Proudfoot, N. J.%% 1991. Poly(A) signals. Cell 64:671–671.
  • Proudfoot, N. J., and G. G. Brownlee. 1976. 3′ non-coding region sequences in eukaryotic messenger RNA. Nature (London) 263:211–214.
  • Rose, M. D., P. Novick, J. H. Thomas, D. Botstein, and G. R. Fink. 1987. A Saccharomyces cerevisiae genomic bank based on a centromere-containing shuttle vector. Gene 60:237–243.
  • Russo, P., W.-Z. Li, D. M. Hampsey, K. S. Zaret, and F. Sherman. 1991. Distinct cis-acting signals enhance 3′ endpoint formation of CYC1 mRNA in the yeast Saccharomyces cerevisiae. EMBO J. 10:563–571.
  • Russo, P., and F. Sherman. 1989. Transcription terminates near the poly(A) site in the CYC1 gene of the yeast Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. USA 86:8348–8352.
  • Sherman, F., and P. P. Slonimski. 1964. Respiration-deficient mutants of yeast. II. Biochemistry. Biochim. Biophys. Acta 90:1–15.
  • Yu, K., and R. T. Elder. 1989. Some of the signals for 3′-end formation in transcription of the Saccharomyces cerevisiae Ty-D15 element are immediately downstream of the initiation site. Mol. Cell. Biol. 9:2431–2444.
  • Zaret, K. S., and F. Sherman. 1982. DNA sequence required for efficient transcription termination in yeast. Cell 28:563–573.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.