Higher plants elaborate much of their architecture post-embryonically
through development initiated at the tips of shoots(1,2) During vegeta
tive growth, leaf primordia arise at predictable sires to give charact
eristic leaf arrangements, or phyllotaxies(3,4). How these sites are d
etermined is a long-standing question(5,6) that bears on the nature of
pattern-formation mechanisms in plants, Fate-mapping studies in sever
al species indicate that each leaf primordium becomes organized from a
group of 100-200 cells on the flank of the shoot apes'. Although mole
cular studies indicate that the regulated expression of specific homeo
box genes plays some part in this determination process(8-11), mechani
sms that regulate the timing and position of leaf initiation are less
well understood. Here we describe a gene from maize, terminal ear 1. P
atterns of expression of this gene in the shoot and phenotypes of muta
nts indicate a role for terminal ear 1 in regulating leaf initiation.
The te1 gene product contains conserved RNA-binding motifs, indicating
that it may function through an RNA-binding activity.