Our understanding of how the 3' ends of mRNAs are formed in plants is
rudimentary compared to what we know about this process in other eukar
yotes. The salient features of plant pre-mRNAs that signal cleavage an
d polyadenylation remain obscure, and the biochemical mechanism is as
yet wholly uncharacterised. Nevertheless, despite the lack of universa
lly conserved cis-acting motifs, a common underlying architecture is e
merging from functional analyses of plant poly(A) signals, allowing me
aningful comparison with components of poly(A) signals in other eukary
otes. A plant poly(A) signal consists of one or more near-upstream ele
ments (NUE), each directing processing at a poly(A) site a short dista
nce downstream of it, and an extensive far-upstream element (FUE) that
enhances processing efficiency at all sites. By analogy with other sy
stems, a model for a plant 3'-end processing complex can be proposed.
Plant poly(A) polymerases have been isolated and partially characteris
ed. These, together with hints that some processing factors are conser
ved in different organisms, opens promising avenues toward initial cha
racterisation of the trans-acting factors involved in 3'-end formation
of mRNAs in higher plants.