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PMID: 2577506 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Deletion analysis of the polyadenylation signal of a pea ribulose-1,5-bisphosphate carboxylase small-subunit gene.

Plant molecular biology ·Vol. 13 ·No. 2 ·1989-08-00 ·Pages 125-38

Hunt AG, MacDonald MH

Abstract

The polyadenylation signal of a pea gene for the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase (rbcS) has been analyzed by deletion mutagenesis and Ti plasmid-mediated gene transfer. Sequences between 6 and 137 bases upstream from the normal polyadenylation sites in this gene (bases -6 to -137) are required for functioning of these sites. In addition, bases -111 to -235 can affect 3' end formation by altering the pattern of 3' termini seen in various transcription units. Sequences between 37 and 95 bases upstream from a cryptic polyadenylation site in this gene [A. G. Hunt, DNA 7: 329-336 (1988)] are necessary for mRNA 3' end formation at this site. At least two different parts of the 3' region of this rbcS gene can serve as a downstream element for polyadenylation at the normal poly(A) addition sites in this gene. Our studies indicate that: 1. the upstream sequences required for polyadenylation in plants are different from those defined in mammalian RNA polymerase II transcription units; 2. sequences 100 or more bases upstream and downstream from poly(A) addition sites in this gene can affect poly(A) addition site choice; and 3. there are apparently redundant downstream elements for polyadenylation in this gene.

Related Genes
MeSH Terms
Base Sequence Chromosome Deletion DNA/genetics DNA Mutational Analysis DNA Probes Fabaceae/genetics,metabolism Molecular Sequence Data Plants/genetics,metabolism Plants, Genetically Modified/genetics,metabolism Plants, Medicinal Plasmids Poly A/genetics,metabolism RNA, Messenger/genetics,metabolism Ribulose-Bisphosphate Carboxylase/genetics,metabolism Transcription, Genetic
Chemicals
DNA Probes RNA, Messenger Poly A DNA Ribulose-Bisphosphate Carboxylase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hunt A G
Department of Agronomy, University of Kentucky, Lexington 40546-0091.
MacDonald M H
References (21)
21 references, click to expand
  1. 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.
    EMBO J. 1986 Nov;5(11):2915-22 PMID: 3024968
  2. Studies on transformation of Escherichia coli with plasmids.
    J Mol Biol. 1983 Jun 5;166(4):557-80 PMID: 6345791
  3. Inhibition of RNA cleavage but not polyadenylation by a point mutation in mRNA 3' consensus sequence AAUAAA.
    Nature. 1983 Oct 13-19;305(5935):600-5 PMID: 6194440
  4. Putative polyadenylation signals in nuclear genes of higher plants: a compilation and analysis.
    Nucleic Acids Res. 1987 Dec 10;15(23):9627-40 PMID: 3697078
  5. Ti plasmid vector for the introduction of DNA into plant cells without alteration of their normal regeneration capacity.
    EMBO J. 1983;2(12):2143-50 PMID: 16453482
  6. Requirement of A-A-U-A-A-A and adjacent downstream sequences for SV40 early polyadenylation.
    Nucleic Acids Res. 1986 Jun 25;14(12):4939-52 PMID: 3014439
  7. Photoregulated expression of a pea rbcS gene in leaves of transgenic plants.
    EMBO J. 1985 Dec 1;4(12):3063-8 PMID: 16453648
  8. Tissue-specific and light-regulated expression of a pea nuclear gene encoding the small subunit of ribulose-1,5-bisphosphate carboxylase.
    EMBO J. 1984 Aug;3(8):1671-9 PMID: 6479146
  9. Design and construction of a versatile system for the expression of foreign genes in plants.
    Gene. 1987;61(1):1-11 PMID: 3443303
  10. Plant cells do not properly recognize animal gene polyadenylation signals.
    Plant Mol Biol. 1987 Jan;8(1):23-35 PMID: 24302521
  11. A functional mRNA polyadenylation signal is required for transcription termination by RNA polymerase II.
    Genes Dev. 1988 Apr;2(4):440-52 PMID: 2836265
  12. Transcription termination within the E1A gene of adenovirus induced by insertion of the mouse beta-major globin terminator element.
    Cell. 1985 Apr;40(4):897-905 PMID: 2580640
  13. mRNA transcripts of several plant genes are polyadenylated at multiple sites in vivo.
    Nucleic Acids Res. 1986 Mar 11;14(5):2229-40 PMID: 3960719
  14. A simple and general method for transferring genes into plants.
    Science. 1985 Mar 8;227(4691):1229-31 PMID: 17757866
  15. Monocot and dicot pre-mRNAs are processed with different efficiencies in transgenic tobacco.
    EMBO J. 1986 Oct;5(10):2419-25 PMID: 16453710
  16. Transcription termination and the regulation of gene expression.
    Annu Rev Biochem. 1986;55:339-72 PMID: 3527045
  17. Analysis of mRNA 3' end formation by modification interference: the only modifications which prevent processing lie in AAUAAA and the poly(A) site.
    EMBO J. 1987 Dec 20;6(13):4177-84 PMID: 3443104
  18. Identification of sequences involved in the polyadenylation of higher plant nuclear transcripts using Agrobacterium T-DNA genes as models.
    EMBO J. 1983;2(3):419-26 PMID: 11894958
  19. Sequencing end-labeled DNA with base-specific chemical cleavages.
    Methods Enzymol. 1980;65(1):499-560 PMID: 6246368
  20. 3' non-coding region sequences in eukaryotic messenger RNA.
    Nature. 1976 Sep 16;263(5574):211-4 PMID: 822353
  21. Identification and characterization of cryptic polyadenylation sites in the 3' region of a pea ribulose-1,5-bisphosphate carboxylase small subunit gene.
    DNA. 1988 Jun;7(5):329-36 PMID: 3042319
Article Info
Journal
Plant molecular biology
Abbr.
Plant Mol Biol
ISSN
0167-4412
Published
1989-08-00
Pages
125-38
Language
English
Region
Netherlands
NLM ID
9106343
Subset
IM
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