Proline rich proteins (PRPs), earlier famous as animal salivary proteins, have now been proven as indispensable plant proteins. They are highly rich in proline amino acid residues at the N-terminus whereas a characteristic eight cysteine motif is located at the C-terminus. The PRPs support a number of developmental processes from germination to plant death. Under normal environmental conditions, PRP genes express customarily in different plant parts depending on the specific function to be carried out. During abiotic stresses, PRP genes exhibit an uneven pattern of transcriptional regulation depending on the time and intensity of stress. Transgenic plants overexpressing PRP genes show an enhanced tolerance to abiotic stresses. This review focuses on contemporary functions of PRPs during stresses and proposes that PRPs are involved in the regulation of free cellular proline content during stress in a well synchronized manner.
In montane Drosophila species, cold-induced plastic changes in energy metabolites are likely developed to cope with cold and starvation stress. Adult Drosophila immigrans reared at 15°C were acclimated at 0°C or 7°C for durations of up to 6 days (fed or unfed conditions). Such flies were tested for plastic changes in resistance to cold or starvation stress as well as for possible accumulation and utilization of four energy metabolites (body lipids, proline, trehalose and glycogen). Adults acclimated at 7°C revealed a greater increase in cold tolerance than flies acclimated at 0°C. Different durations of cold acclimation at 7°C led to increased level of body lipids only in fed flies which were utilized under starvation stress. However, such plastic responses were not observed in the flies acclimated at 0°C, which remained unfed due to chill-coma. These observations suggest a possible role of feeding to improve starvation resistance only in the flies acclimated at 7°C with food. Cold acclimated D. immigrans flies revealed improved cold resistance through a possible reshuffling of trehalose and glycogen; and starvation-induced proline which was utilized under cold stress durations. Finally, greater reduction in mean daily fecundity due to cold or starvation was observed in 0°C acclimated flies as compared to 7°C acclimated flies. Thus, cold acclimation conditions (0°C or 7°C) greatly impact resistance to cold and starvation in D. immigrans.
Plastic responses to multiple environmental stressors in wet or dry seasonal populations of tropical Drosophila species have received less attention. We tested plastic effects of heat hardening, acclimation to drought or starvation, and changes in trehalose, proline and body lipids in Drosophila ananassae flies reared under wet or dry season-specific conditions. Wet season flies revealed significant increase in heat knockdown, starvation resistance and body lipids after heat hardening. However, accumulation of proline was observed only after desiccation acclimation of dry season flies while wet season flies elicited no proline but trehalose only. Therefore, drought-induced proline can be a marker metabolite for dry-season flies. Further, partial utilization of proline and trehalose under heat hardening reflects their possible thermoprotective effects. Heat hardening elicited cross-protection to starvation stress. Stressor-specific accumulation or utilization as well as rates of metabolic change for each energy metabolite were significantly higher in wet-season flies than dry-season flies. Energy metabolite changes due to inter-related stressors (heat versus desiccation or starvation) resulted in possible maintenance of energetic homeostasis in wet- or dry-season flies. Thus, low or high humidity-induced plastic changes in energy metabolites can provide cross-protection to seasonally varying climatic stressors.
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