EXPRESSION OF GENES FOR PHENYLALANINE AMMONIA-LYASE AND 8-HYDROXY-3-METHYLGLUTARYL COA REDUCTASE IN AGED POTATO-TUBERS INFECTED WITH PHYTOPHTHORA-INFESTANS

Citation
H. Yoshioka et al., EXPRESSION OF GENES FOR PHENYLALANINE AMMONIA-LYASE AND 8-HYDROXY-3-METHYLGLUTARYL COA REDUCTASE IN AGED POTATO-TUBERS INFECTED WITH PHYTOPHTHORA-INFESTANS, Plant and Cell Physiology, 37(1), 1996, pp. 81-90
Citations number
54
Categorie Soggetti
Plant Sciences
Journal title
ISSN journal
00320781
Volume
37
Issue
1
Year of publication
1996
Pages
81 - 90
Database
ISI
SICI code
0032-0781(1996)37:1<81:EOGFPA>2.0.ZU;2-H
Abstract
In comparison with tissues of unaged potato tubers, tissues of aged tu bers rapidly express features of resistance, such as hypersensitive ce ll death, browning and the accumulation of phytoalexins in response to infection by an incompatible race of Phytophthora infestans. Expressi on of two putative defense genes, namely, genes for 3-hydroxy-3-methyl glutaryl CoA reductase (HMGR) and phenylalanine ammonia-lyase (PAL), a nd the activities of the corresponding enzymes were determined in aged , inoculated potato discs. The level of HMGR activity was higher after inoculation with an incompatible than with a compatible race of the p athogen. The levels of the transcripts in the total RNA were, however, nearly identical in both cases. When we examined polysomal RNA, we fo und an enhanced level of transcripts for HMGR only in tissues that had been infected with the incompatible race. Furthermore, comparison of the patterns of distribution of HMGR mRNA associated with polysomes in two gradients revealed modulation of HMGR at the level of initiation of translation. These results suggest that the activity of HMGR in age d potato tubers that have been attacked by P. infestans might be regul ated, in part, at the post-transcriptional level in a race-cultivar-sp ecific manner. By contrast, the levels of PAL mRNA in both the total a nd the polysomal RNA fractions, as well as the enzymatic activity, wer e higher in the incompatible than in the compatible interaction. The r esults suggest that the activity of PAL is regulated differentially at the transcriptional level during the interactions.