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A near-upstream element in a plant polyadenylation signal consists of more than six nucleotides

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Abstract

A plant polyadenylation signal consists of three distinct components: a far-upstream element (FUE) that can control utilization of several polyadenylation sites, one or more near-upstream elements (NUEs) that control utilization of each site in a transcription unit, and polyadenylation site (CSs) themselves. NUEs have previously been suggested to be related to the mammalian polyadenylation signal AAUAAA. However, many plant genes do not contain AAUAAA-like motifs near their polyadenylation sites. To better understand the nature of NUEs, we conducted a systematic analysis of the NUE for one polyadenylation site (site 1) in the pea rbcS-E9 gene; this NUE lacks an AAUAAA motif. Linker substitution studies showed that the NUE for site 1 in this gene resides in the sequence AAAUGGAAA. Single-nucleotide substitutions in this domain had modest effects on the functioning of this NUE. Replacement of part of this sequence with the sequence AAUAAA increased the efficiency of this NUE. However, alteration of nucleotides immediately 3′ of the AAUAAA reversed this effect. Our results indicate that the NUE for site 1 consists of as many as 9 nucleotides, that these 9 bases do not include an element that is intolerant of single base changes, that the sequence AAUAAA can function as a NUE for site 1, and that sequences flanking AAUAAA can affect the efficiency of functioning as a NUE.

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References

  1. Connelly S, Manley JL: A functional mRNA polyadenylation signal is required for transcription termination by RNA polymerase II. Genes Devel 2: 440–452 (1988).

    Google Scholar 

  2. Falck-Pedersen E, Logan J, Shenk T, Darnell JE: Transcription termination within the E1A gene of adenovirus induced by the insertion of the mouse β-major globin terminator element. Cell 40: 897–905 (1985).

    Google Scholar 

  3. Heidmann S, Schindewolf C, Stumpf G, Domdey H: Flexibility and interchangeability of polyadenylation signals in Saccharomyces cerevisiae. Mol Cell Biol 14: 4633–4642 (1994).

    Google Scholar 

  4. Hunt AG: Identification and characterization of cryptic polyadenylation sites in the 3′ region of a pea ribulose-1,5-bisphosphate carboxylase small subunit gene. DNA 7: 329–336 (1988).

    Google Scholar 

  5. Hunt AG: Messenger RNA 3′ end formation in plants. Annu Rev Plant Physiol Plant Mol Biol 45: 47–60 (1994).

    Google Scholar 

  6. Irniger S, Sanfaçon H, Egli CM, Braus GH: Different sequence elements are required for function of the cauli-flower mosaic virus polyadenylation site in Saccharomyces cerevisiae compared with plants. Mol Cell Biol 12: 2322–2330 (1992).

    Google Scholar 

  7. Luehrsen KR, Walbot V: Intron creation and polyadenylation in maize are directed by AU-rich RNA. Genes Devel 8: 1117–1130 (1994).

    Google Scholar 

  8. MacDonald MH, Mogen BD, Hunt AG: Characterization of the polyadenylation signal of the T-DNA-encoded octopine synthase gene. Nucl Acids Res 19: 5575–5581 (1991).

    Google Scholar 

  9. Mogen BD, MacDonald MH, Graybosch R, Hunt AG: Upstream sequences other than AAUAAA are required for efficient messenger RNA 3′ end formation in plants. Plant Cell 2: 1261–1272 (1990).

    Google Scholar 

  10. Mogen BD, MacDonald MH, Leggewie G, Hunt AG: Several distinct types of sequence elements are required for efficient mRNA 3′ end formation in a pea rbcS gene. Mol Cell Biol 12: 5406–5414 (1992).

    Google Scholar 

  11. Niwa M, Berget SM: Mutation of the AAUAAA polyadenylation signal depresses in vitro splicing of proximal but not distal introns. Genes Devel 5: 2086–2095 (1991).

    Google Scholar 

  12. Niwa M, Rose SD, Berget SM: In vitro polyadenylation is stimulated by the presence of an upstream intron. Genes Devel 4: 1552–1559 (1990).

    Google Scholar 

  13. Ohtsubo N, Iwabuchi M: The conserved 3′-flanking sequence, AATGGAAATG, of the wheat histone H3 gene is necessary for the accurate 3′-end formation of mRNA. Nucl Acids Res 22: 1052–1058 (1994).

    Google Scholar 

  14. Proudfoot NJ: Poly[A] signals. Cell 64: 671–674 (1991).

    Google Scholar 

  15. Rothnie HM, Reid J, Hohn T: The contribution of AAUAAA and the upstream element UUUGUA to the efficiency of mRNA 3′ end formation in plants. EMBO J 13: 2200–2210 (1994).

    Google Scholar 

  16. Russo P, Li WZ, Guo Z, Sherman F: Signals that produce 3′ termini in CYC1 mRNA of the yeast Saccharomyces cerevisiae. Mol Cell Biol 13: 7836–7849 (1993).

    Google Scholar 

  17. Russo P, Sherman F: Transcription terminates near the poly(A) site in the CYC1 gene of the yeast Saccharomyces cerevisiae. Proc Natl Acad Sci USA 86: 8348–8352 (1989).

    Google Scholar 

  18. Sachs A, Wahle E: Poly(A) tail metabolism and function in eucaryotes. J Biol Chem 268: 22955–22958 (1993).

    Google Scholar 

  19. Sanfaçon H: Analysis of figwort mosaic virus (plant pararetrovirus) polyadenylation signal. Virology 198: 39–49 (1994).

    Google Scholar 

  20. Sanfaçon H, Brodmann P, Hohn T: A dissection of the cauliflower mosaic virus polyadenylation signal. Genes Devel 5: 141–149 (1991).

    Google Scholar 

  21. Sheets M, Ogg S, Wickens M: Point mutations in AAUAAA and the poly(A) addition site: effects on the accuracy and efficiency of cleavage and polyadenylation in vitro. Nucl Acids Res 18: 5799–5805 (1990).

    Google Scholar 

  22. Wahle E, Keller W: The biochemistry of 3′-end cleavage and polyadenylation of messenger RNA precursors. Annu Rev Biochem 61: 419–440 (1992).

    Google Scholar 

  23. Whitelaw E, Proudfoot N: α-Thallassaemia caused by a poly(A) site mutation reveals that transcriptional termination is linked to 3′ end processing in the human α-2 globin gene. EMBO J 5: 2915–2922 (1986).

    Google Scholar 

  24. Wu L, Ueda T, Messing J: 3′-end processing of the maize 27 kDa zein mRNA. Plant J 4: 535–544 (1993).

    Google Scholar 

  25. Wu L, Ueda T, Messing J: Sequence and spatial requirements for the tissue- and species- independent 3′-end processing mechanism of plant mRNA. Mol Cell Biol 14: 6829–6838 (1994).

    Google Scholar 

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Li, Q., Hunt, A.G. A near-upstream element in a plant polyadenylation signal consists of more than six nucleotides. Plant Mol Biol 28, 927–934 (1995). https://doi.org/10.1007/BF00042076

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