Lipid bodies are present in most plant cells and not just in storage tissue
s, such as seeds, as is often assumed. There is a growing number of protein
s that are associated with lipid bodies in different plant tissues. In seed
s, the most common class of lipid-body protein is the oleosins, which are f
ound on the surfaces on lipid bodies in all desiccation tolerant plants but
are absent from lipid bodies in the seeds of desiccation-sensitive plants,
e.g. cocoa or neem. The absence of oleosins in these seeds is not. problem
atic during dehydration but leads to a fatal coalescence of lipid bodies af
ter germination, A class of anther-specific proteins has a precursor form t
hat contains an oleosin-like hydrophobic domain and is initially localised
on lipid bodies in the tapetum. However, the oleosin-like domain is cleaved
off after release into the anther locule and the mature proteins, which ar
e the major protein components of the pollen coat, contain no oleosin-like
sequences. Therefore these proteins, which have been named "pollenins", use
their oleosin-like domain as a novel form of cleavable targeting sequence.
A third type of lipid-body protein is caleosin, which also has endoplasmic
reticulum associated isoforms and may be involved in lipid-body biogenesis
and membrane trafficking. Analysis of the expression patterns of oleosin a
nd caleosin genes/proteins revealed an unexpected localisation in young roo
t tips, as confirmed by expressing promoter-GUS constructs in transgenic pl
ants. Several other classes of storage product-related genes hitherto belie
ved to seed-specific are also transiently expressed in root tips following
seed germination, We discuss the implications of these findings for root de
velopment and the use of "seed-specific" gene promoters in general.