Small heat shock proteins and stress tolerance in plants.

By Weining Sun, M. Van Montagu, N. Verbruggen. Biochimica et Biophysica Acta, 2002

646 citations recorded by the source corpus.

Subfields: Insect Science, Materials Chemistry, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/06ce0a18f0994f5645756a4bc03c5654d69ba336

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Citations in the corpus

Physiology and molecular biology of stress tolerance in plants (2006, background): “Expression of heat shock proteins and heat shock factors (proteinaceous factors that stimulate expression of heat shock proteins as well as other heat tolerance genes) results in increased thermotolerance in many plants (Sun et al., 2002).”
Small heat shock proteins genes are differentially expressed in distinct varieties of common bean (2003, background): “In the absence of environmental stress, the sHSP expression in plants is restricted to certain stages of development such as embryogenesis, germination, pollen development, and fruit maturation (Sun et al., 2002).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “The resultant plasmid has the”
Plant heat-shock proteins: A mini review (2011, neutral): “The sHsps cannot refold non-native proteins, but they can bind to partially folded or denatured substrates proteins, preventing irreversible unfolding or wrong protein aggregation (Sun et al., 2002).”
Plant tolerance to high temperature in a changing environment: scientific fundamentals and production of heat stress-tolerant crops (2013, background): “Of the HSP gene family, induction of small HSP gene expression and protein accumulation upon environmental stresses point to the hypothesis that these proteins play an important role in stress tolerance (Sun et al., 2002).”
Cold stress and acclimation - what is important for metabolic adjustment? (2010, background): “Small HSPs are not themselves able to refold non-native proteins, but do facilitate refolding effected by HSP70 and HSP100 (Sun et al. 2002; Mogk et al. 2003).”
Gene function beyond the single trait: natural variation, gene effects, and evolutionary ecology in Arabidopsis thaliana (2005, background): “…to CO 2 concentration are strongly dependent on the environment, in particular to drought stress (Woodward et al. 2002) and N concentration [mutant studies: (Sun et al. 2002), natural accessions: (Zhang & Lechowicz 1995)] but still the mechanistic basis of this variation is poorly understood.”
Growth, lipid peroxidation and photosynthesis in two tall fescue cultivars differing in heat tolerance (2009, background): “Chloroplasts are the main sites for generating ROS under both stressed and unstressed conditions, and it is one of the organelles in leaf tissues of plants most sensitive to high temperature stress (Xu et al. 1995, Sun et al. 2002).”