Upstream sequences other than AAUAAA are required for efficient messenger RNA 3'-end formation in plants.
Open Access
- 1 December 1990
- journal article
- Published by Oxford University Press (OUP) in Plant Cell
- Vol. 2 (12) , 1261-1272
- https://doi.org/10.1105/tpc.2.12.1261
Abstract
We have characterized the upstream nucleotide sequences involved in mRNA 39-end formation in the 39 regions of the cauliflower mosaic virus (CaMV) 19S/35S transcription unit and a pea gene encoding ribulose-1,5-bisphosphate carboxylase small subunit (rbcS). Sequences between 57 bases and 181 bases upstream from the CaMV polyadenylation site were required for efficient polyadenylation at this site. In addition, an AAUAAA sequence located 13 bases to 18 bases upstream from this site was also important for efficient mRNA 39-end formation. An element located between 60 bases and 137 bases upstream from the poly(A) addition sites in a pea rbcS gene was needed for functioning of these sites. The CaMV -181/-57 and rbcS -137/-60 elements were different in location and sequence composition from upstream sequences needed for polyadenylation in mammalian genes, but resembled the signals that direct mRNA 39-end formation in yeast. However, the role of the AAUAAA motif in 39-end formation in the CaMV 39 region was reminiscent of mRNA polyadenylation in animals. We suggest that multiple elements are involved in mRNA 39-end formation in plants, and that interactions of different components of the plant polyadenylation apparatus with their respective sequence elements and with each other are needed for efficient mRNA 39-end formation.Keywords
This publication has 24 references indexed in Scilit:
- Proximity to the promoter inhibits recognition of cauliflower mosaic virus polyadenylation signalNature, 1990
- Different 3' end regions strongly influence the level of gene expression in plant cells.Plant Cell, 1989
- 3′ cleavage and polyadenylation of mRNA precursors in vitro requires a poly(A) polymerase, a cleavage factor, and a snRNPCell, 1988
- Identification and Characterization of Cryptic Polyadenylation Sites in the 3′ Region of a Pea Ribulose-1,5-Bisphosphate Carboxylase Small Subunit GeneDNA, 1988
- Multiple factors are required for poly(A) addition to a mRNA 3' end.Genes & Development, 1988
- Multiple factors are required for specific RNA cleavage at a poly(A) addition site.Genes & Development, 1988
- A functional mRNA polyadenylation signal is required for transcription termination by RNA polymerase II.Genes & Development, 1988
- Separation and characterization of a poly(A) polymerase and a cleavage/specificity factor required for pre-mRNA polyadenylationCell, 1988
- TRANSCRIPTION TERMINATION AND THE REGULATION OF GENE EXPRESSIONAnnual Review of Biochemistry, 1986
- Requirement of a downstream sequence for generation of a poly(A) addition siteCell, 1984