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. 1997 Sep 1;25(17):3465–3470. doi: 10.1093/nar/25.17.3465

Specific polyadenylation and purification of total messenger RNA from Escherichia coli.

R R Amara 1, S Vijaya 1
PMCID: PMC146910  PMID: 9254705

Abstract

Obtaining pure mRNA preparations from prokaryotes has been difficult, if not impossible, for want of a poly(A) tail on these messages. We have used poly(A) polymerase from yeast to effect specific polyadenylation of Escherichia coli polysomal mRNA in the presence of magnesium and manganese. The polyadenylated total mRNA, which could be subsequently purified by binding to and elution from oligo(dT) beads, had a size range of 0.4-4.0 kb. We have used hybridization to a specific plasmid-encoded gene to further confirm that the polyadenylated species represented mRNA. Withdrawal of Mg2+ from the polyadenylation reaction resulted in addition of poly(A) to 16S rRNA despite the presence of Mn2+, indicating the vital role of Mg2+ in maintaining the native structure of polysomes. Complete dissociation of polysomes into ribosomal subunits resulted in quantitative polyadenylation of both 16S and 23S rRNA species. Chromosomal lacZ gene-derived messages were quantitatively recovered in the oligo(dT)-bound fraction, as demonstrated by RT-PCR analysis. Potential advantages that accrue from the availability of pure total mRNA from prokaryotes is discussed.

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Selected References

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  1. Abu Kwaik Y., Pederson L. L. The use of differential display-PCR to isolate and characterize a Legionella pneumophila locus induced during the intracellular infection of macrophages. Mol Microbiol. 1996 Aug;21(3):543–556. doi: 10.1111/j.1365-2958.1996.tb02563.x. [DOI] [PubMed] [Google Scholar]
  2. Jay G., Kaempfer R. Initiation of protein synthesis. Binding of messenger RNA. J Biol Chem. 1975 Aug 10;250(15):5742–5748. [PubMed] [Google Scholar]
  3. Lee S. W., Tomasetto C., Sager R. Positive selection of candidate tumor-suppressor genes by subtractive hybridization. Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2825–2829. doi: 10.1073/pnas.88.7.2825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Liang P., Pardee A. B. Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction. Science. 1992 Aug 14;257(5072):967–971. doi: 10.1126/science.1354393. [DOI] [PubMed] [Google Scholar]
  5. Lingner J., Radtke I., Wahle E., Keller W. Purification and characterization of poly(A) polymerase from Saccharomyces cerevisiae. J Biol Chem. 1991 May 15;266(14):8741–8746. [PubMed] [Google Scholar]
  6. Moazed D., Van Stolk B. J., Douthwaite S., Noller H. F. Interconversion of active and inactive 30 S ribosomal subunits is accompanied by a conformational change in the decoding region of 16 S rRNA. J Mol Biol. 1986 Oct 5;191(3):483–493. doi: 10.1016/0022-2836(86)90143-9. [DOI] [PubMed] [Google Scholar]
  7. Nakazato H., Venkatesan S., Edmonds M. Polyadenylic acid sequences in E. coli messenger RNA. Nature. 1975 Jul 10;256(5513):144–146. doi: 10.1038/256144a0. [DOI] [PubMed] [Google Scholar]
  8. Perry R. P., Kelley D. E., LaTorre J. Lack of polyadenylic acid sequences in the messenger RNA of E. coli. Biochem Biophys Res Commun. 1972 Sep 26;48(6):1593–1600. doi: 10.1016/0006-291x(72)90896-0. [DOI] [PubMed] [Google Scholar]
  9. Perry R. P., La Torre J., Kelley D. E., Greenberg J. R. On the lability of poly(A) sequences during extraction of messenger RNA from polyribosomes. Biochim Biophys Acta. 1972 Mar 14;262(2):220–226. doi: 10.1016/0005-2787(72)90236-5. [DOI] [PubMed] [Google Scholar]
  10. Roskoski R., Jr Role of divalent cations on the association of rat liver ribosomal subunits. Arch Biochem Biophys. 1969 Mar;130(1):561–566. doi: 10.1016/0003-9861(69)90071-x. [DOI] [PubMed] [Google Scholar]
  11. Studier F. W., Rosenberg A. H., Dunn J. J., Dubendorff J. W. Use of T7 RNA polymerase to direct expression of cloned genes. Methods Enzymol. 1990;185:60–89. doi: 10.1016/0076-6879(90)85008-c. [DOI] [PubMed] [Google Scholar]
  12. Tal M. Metal ions and ribosomal conformation. Biochim Biophys Acta. 1969 Nov 19;195(1):76–86. doi: 10.1016/0005-2787(69)90604-2. [DOI] [PubMed] [Google Scholar]
  13. Tissieres A., Schlessinger D., Gros F. AMINO ACID INCORPORATION INTO PROTEINS BY ESCHERICHIA COLI RIBOSOMES. Proc Natl Acad Sci U S A. 1960 Nov;46(11):1450–1463. doi: 10.1073/pnas.46.11.1450. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Weiss R. L., Kimes B. W., Morris D. R. Cations and ribosome structure. 3. Effects on the 30S and 50S subunits of replacing bound Mg 2+ by inorganic cations. Biochemistry. 1973 Jan 30;12(3):450–456. doi: 10.1021/bi00727a014. [DOI] [PubMed] [Google Scholar]
  15. Weiss R. L., Morris D. R. Cations and ribosome structure. I. Effects on the 30S subunit of substituting polyamines for magnesium ion. Biochemistry. 1973 Jan 30;12(3):435–441. doi: 10.1021/bi00727a012. [DOI] [PubMed] [Google Scholar]

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