Transgenic potato plants expressing soybean beta-1,3-endoglucanase gene exhibit an increased resistance to Phytophthora infestans.

Soybean beta-1,3-endoglucanase represents a model system for studies on early plant responses to infection by fungal pathogens, and it has been implicated in the release of elicitors from fungal cell walls. In the present study, potato plants were transformed with the soybean beta-1,3-endoglucanase cDNA via Agrobacterium delivery system. The transfer of the gene into potato genome was confirmed by (i) PCR amplification, (ii) Northern blot analyses, and (iii) an increase in the activity of beta-1,3-endoglucanase in transgenic plants. The transformation resulted in an increased resistance of selected transgenic plants to infection by Phytophthora infestans, an important pathogen.

Protein-synthesizing activity of maize-shoot chromatin : I. Conditions and component requirements.

The evidence presented in this paper suggests that purified plant chromatin, similar to mammalian (SR Umansky et al., Eur J Biochem 1980 105: 117-129), has the ability to incorporate amino acids into acid precipitable material. The polypeptide-synthesizing system of chromatin seems to differ substantially from the classical polyribosomal translation mechanism in cytoplasm. When chromatin purified from 5-day-old etiolated maize (Zea mays) shoots was incubated with (14)C-labeled amino acids, label was incorporated into the trichloroacetic acid precipitable product. Chloramphenicol, pactamycin, and actinomycin D inhibited the incorporation almost completely, whereas treatment with cycloheximide, puromycin, or aurintricarboxylic acid did not affect the labeling. Preincubation with pancreatic RNase was also without effect, but treatment of chromatin with DNase I caused about 25% depression of label incorporation. A wheat germ translation system or its single components have no effect on the chromatin polypeptide-synthesizing activity beyond that expected for a simple addition. The protein-synthesizing system is tightly bound to chromatin and could not be removed by dissociation in 1 molar NaCl. The mean molecular weight of the major protein fraction synthesized in the presence of chromatin was 21 to 24 kilodaltons.

RNA synthesis in newly isolated and cultivated mesophyll protoplasts.

Tobacco leaf mesophyll protoplasts exhibit low incorporation of [3H]uridine and 32P into RNA, up to 12 h of cultivation, irrespective of the presence of phytohormones. After 24 h of cultivation a dramatic increase in RNA synthesis is observed; it is the highest in the heterogeneous nucleoplasmic RNA fraction. The protoplasts cultivated in the absence of phytohormones show lower incorporation of precursors.

Preferential stimulation of the plant mRNA synthesis by gibberellic acid.

1. Treatment of the etiolated maize seedlings with the plant hormone, gibberellic acid results in a significant enhancement of heavy polyribosome formation. 2. This is accompanied by highly increased incorporation of the labelled RNA precursors into RNA engaged in the polyribosomal complex, as well as by an increased rate of protein synthesis in vivo. 3. Determination of the specific radioactivity of particular RNA classes isolated from polyribosomes reveals that gibberellic acid stimulates mostly the synthesis of the rapidly labelled, non-ribosomal RNA fraction. 4. A considerable amount of this rapidly labelled RNA fraction, whose synthesis is preferentially stimulated by exogenous gibberellic acid contains poly(A) sequences, as shown by affinity chromatography on oligo (dT)-cellulose indicating that phytohormone causes an increased transcription of mRNA in etiolated maize seedlings. 5. When [3H]adenosine served as the RNA precursor it was found that the ratio between the heteropolymeric and polyadenylic parts of the poly(A)-RNA chain markedly changed under gibberellin treatment, suggesting that, in addition to an increased rate of mRNA synthesis, the plant hormone also affects the process of post-transcriptional polyadenylation of the newly made mRNA precursors. Possible extension of the polyadenylate segment in the presence of gibberellin may account for a longer functional half-life of the mRNA synthesized in plants treated with the phytohormone, and may explain significantly enhanced heavy polyribosome formation, as well as a higher efficiency of protein synthesis in plants treated with gibberellic acid.