Leucine aminopeptidase RNAs, proteins, and activities increase in responseto water deficit, salinity, and the wound signals systemin, methyl jasmonate, and abscisic acid
Ws. Chao et al., Leucine aminopeptidase RNAs, proteins, and activities increase in responseto water deficit, salinity, and the wound signals systemin, methyl jasmonate, and abscisic acid, PLANT PHYSL, 120(4), 1999, pp. 979-992
LapA RNAs, proteins, and activities increased in response to systemin, meth
yl jasmonate, abscisic acid (ABA), ethylene, water deficit, and salinity in
tomato (Lycopersicon esculentum). Salicylic acid inhibited wound-induced i
ncreases of LapA RNAs. Experiments using the ABA-deficient flacca mutant in
dicated that ABA was essential for wound and systemin induction of LapA, an
d ABA and systemin acted synergistically to induce LapA gene expression. in
contrast, pin2 (proteinase inhibitor 2) was not dependent on exogenous ABA
. Whereas both LapA and le4 (L. esculentum dehydrin) were up-regulated by i
ncreases in ABA, salinity, and water deficit, only LapA was regulated by oc
tadecanoid pathway signals. Comparison of LapA expression with that of the
PR-1 (pathogenesis-related 1) and GluB (basic beta-1,3-glucanase) genes ind
icated that these PR protein genes were modulated by a systemin-independent
jasmonic acid-signaling pathway. These studies showed that at least four s
ignaling pathways were utilized during tomato wound and defense responses.
Analysis of the expression of a LapA1:GUS gene in transgenic plants indicat
ed that the LapA I promoter was active during floral and fruit development
and was used during vegetative growth only in response to wounding, Pseudom
onas syringae pv tomato infection, or wound signals. This comprehensive und
erstanding of the regulation of LapA genes indicated that this regulatory p
rogram is distinct from the wound-induced pin2, ABA-responsive le4, and PR
protein genes.