Protein Cryoprotective Activity of a Cytosolic Small Heat Shock Protein That Accumulates Constitutively in Chestnut Stems and Is Up-Regulated by Low and High Temperatures

Heat shock, and other stresses that cause protein misfolding and aggregation, trigger the accumulation of heat shock proteins (HSPs) in virtually all organisms. Among the HSPs of higher plants, those belonging to the small HSP (sHSP) family remain the least characterized in functional terms. We anal...

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Published inPlant physiology (Bethesda) Vol. 134; no. 4; pp. 1708 - 1717
Main Authors Maria-Angeles Lopez-Matas, Paulina Nuñez, Alvaro Soto, Allona, Isabel, Casado, Rosa, Collada, Carmen, Maria-Angeles Guevara, Aragoncillo, Cipriano, Gomez, Luis
Format Journal Article
LanguageEnglish
Published Rockville, MD American Society of Plant Biologists 01.04.2004
American Society of Plant Physiologists
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RNA
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Abstract Heat shock, and other stresses that cause protein misfolding and aggregation, trigger the accumulation of heat shock proteins (HSPs) in virtually all organisms. Among the HSPs of higher plants, those belonging to the small HSP (sHSP) family remain the least characterized in functional terms. We analyzed the occurrence of sHSPs in vegetative organs of Castanea sativa (sweet chestnut), a temperate woody species that exhibits remarkable freezing tolerance. A constitutive sHSP subject to seasonal periodic changes of abundance was immunodetected in stems. This protein was identified by matrix-assisted laser-desorption ionization time of flight mass spectrometry and internal peptide sequencing as CsHSP17.5, a cytosolic class I sHSP previously described in cotyledons. Expression of the corresponding gene in stems was confirmed through cDNA cloning and reverse transcription-PCR. Stem protein and mRNA profiles indicated that CsHSP17.5 is significantly up-regulated in spring and fall, reaching maximal levels in late summer and, especially, in winter. In addition, cold exposure was found to quickly activate shsp gene expression in both stems and roots of chestnut seedlings kept in growth chambers. Our main finding is that purified CsHSP17.5 is very effective in protecting the cold-labile enzyme lactate dehydrogenase from freeze-induced inactivation (on a molar basis, CsHSP17.5 is about 400 times more effective as cryoprotectant than hen egg-white lysozyme). Consistent with these observations, repeated freezing/thawing did not affect appreciably the chaperone activity of diluted CsHSP17.5 nor its ability to form dodecameric complexes in vitro. Taken together, these results substantiate the hypothesis that sHSPs can play relevant roles in the acquisition of freezing tolerance.
AbstractList Heat shock, and other stresses that cause protein misfolding and aggregation, trigger the accumulation of heat shock proteins (HSPs) in virtually all organisms. Among the HSPs of higher plants, those belonging to the small HSP (sHSP) family remain the least characterized in functional terms. We analyzed the occurrence of sHSPs in vegetative organs of Castanea sativa (sweet chestnut), a temperate woody species that exhibits remarkable freezing tolerance. A constitutive sHSP subject to seasonal periodic changes of abundance was immunodetected in stems. This protein was identified by matrix-assisted laser-desorption ionization time of flight mass spectrometry and internal peptide sequencing as CsHSP17.5, a cytosolic class I sHSP previously described in cotyledons. Expression of the corresponding gene in stems was confirmed through cDNA cloning and reverse transcription-PCR. Stem protein and mRNA profiles indicated that CsHSP17.5 is significantly up-regulated in spring and fall, reaching maximal levels in late summer and, especially, in winter. In addition, cold exposure was found to quickly activate shsp gene expression in both stems and roots of chestnut seedlings kept in growth chambers. Our main finding is that purified CsHSP17.5 is very effective in protecting the cold-labile enzyme lactate dehydrogenase from freeze-induced inactivation (on a molar basis, CsHSP17.5 is about 400 times more effective as cryoprotectant than hen egg-white lysozyme). Consistent with these observations, repeated freezing/thawing did not affect appreciably the chaperone activity of diluted CsHSP17.5 nor its ability to form dodecameric complexes in vitro. Taken together, these results substantiate the hypothesis that sHSPs can play relevant roles in the acquisition of freezing tolerance.
Heat shock, and other stresses that cause protein misfolding and aggregation, trigger the accumulation of heat shock proteins (HSPs) in virtually all organisms. Among the HSPs of higher plants, those belonging to the small HSP (sHSP) family remain the least characterized in functional terms. We analyzed the occurrence of sHSPs in vegetative organs of Castanea sativa (sweet chestnut), a temperate woody species that exhibits remarkable freezing tolerance. A constitutive sHSP subject to seasonal periodic changes of abundance was immunodetected in stems. This protein was identified by matrix-assisted laser-desorption ionization time of flight mass spectrometry and internal peptide sequencing as CsHSP17.5, a cytosolic class I sHSP previously described in cotyledons. Expression of the corresponding gene in stems was confirmed through cDNA cloning and reverse transcription-PCR. Stem protein and mRNA profiles indicated that CsHSP17.5 is significantly up-regulated in spring and fall, reaching maximal levels in late summer and, especially, in winter. In addition, cold exposure was found to quickly activate shsp gene expression in both stems and roots of chestnut seedlings kept in growth chambers. Our main finding is that purified CsHSP17.5 is very effective in protecting the cold-labile enzyme lactate dehydrogenase from freeze-induced inactivation (on a molar basis, CsHSP17.5 is about 400 times more effective as cryoprotectant than hen egg-white lysozyme). Consistent with these observations, repeated freezing/thawing did not affect appreciably the chaperone activity of diluted CsHSP17.5 nor its ability to form dodecameric complexes in vitro. Taken together, these results substantiate the hypothesis that sHSPs can play relevant roles in the acquisition of freezing tolerance.Heat shock, and other stresses that cause protein misfolding and aggregation, trigger the accumulation of heat shock proteins (HSPs) in virtually all organisms. Among the HSPs of higher plants, those belonging to the small HSP (sHSP) family remain the least characterized in functional terms. We analyzed the occurrence of sHSPs in vegetative organs of Castanea sativa (sweet chestnut), a temperate woody species that exhibits remarkable freezing tolerance. A constitutive sHSP subject to seasonal periodic changes of abundance was immunodetected in stems. This protein was identified by matrix-assisted laser-desorption ionization time of flight mass spectrometry and internal peptide sequencing as CsHSP17.5, a cytosolic class I sHSP previously described in cotyledons. Expression of the corresponding gene in stems was confirmed through cDNA cloning and reverse transcription-PCR. Stem protein and mRNA profiles indicated that CsHSP17.5 is significantly up-regulated in spring and fall, reaching maximal levels in late summer and, especially, in winter. In addition, cold exposure was found to quickly activate shsp gene expression in both stems and roots of chestnut seedlings kept in growth chambers. Our main finding is that purified CsHSP17.5 is very effective in protecting the cold-labile enzyme lactate dehydrogenase from freeze-induced inactivation (on a molar basis, CsHSP17.5 is about 400 times more effective as cryoprotectant than hen egg-white lysozyme). Consistent with these observations, repeated freezing/thawing did not affect appreciably the chaperone activity of diluted CsHSP17.5 nor its ability to form dodecameric complexes in vitro. Taken together, these results substantiate the hypothesis that sHSPs can play relevant roles in the acquisition of freezing tolerance.
Heat shock, and other stresses that cause protein misfolding and aggregation, trigger the accumulation of heat shock proteins (HSPs) in virtually all organisms. Among the HSPs of higher plants, those belonging to the small HSP (sHSP) family remain the least characterized in functional terms. We analyzed the occurrence of sHSPs in vegetative organs of Castanea sativa (sweet chestnut), a temperate woody species that exhibits remarkable freezing tolerance. A constitutive sHSP subject to seasonal periodic changes of abundance was immunodetected in stems. This protein was identified by matrix-assisted laser-desorption ionization time of flight mass spectrometry and internal peptide sequencing as CsHSP17.5, a cytosolic class I sHSP previously described in cotyledons. Expression of the corresponding gene in stems was confirmed through cDNA cloning and reverse transcription-PCR. Stem protein and mRNA profiles indicated that CsHSP17.5 is significantly up-regulated in spring and fall, reaching maximal levels in late summer and, especially, in winter. In addition, cold exposure was found to quickly activate shsp gene expression in both stems and roots of chestnut seedlings kept in growth chambers. Our main finding is that purified CsHSP17.5 is very effective in protecting the cold-labile enzyme lactate dehydrogenase from freeze-induced inactivation (on a molar basis, CsHSP17.5 is about 400 times more effective as cryoprotectant than hen egg-white lysozyme). Consistent with these observations, repeated freezing/thawing did not affect appreciably the chaperone activity of diluted CsHSP17.5 nor its ability to form dodecameric complexes in vitro. Taken together, these results substantiate the hypothesis that sHSPs can play relevant roles in the acquisition of freezing tolerance.
Author Alvaro Soto
Paulina Nuñez
Maria-Angeles Guevara
Gomez, Luis
Collada, Carmen
Allona, Isabel
Aragoncillo, Cipriano
Casado, Rosa
Maria-Angeles Lopez-Matas
AuthorAffiliation Departamento de Biotecnología, Escuela Técnica Superior de Ingenieros de Montes, Universidad Politecnica de Madrid, E–28040 Madrid, Spain
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Issue 4
Keywords Temperature
Cotyledon
Cold
Root
Transcription
Enzyme
Growth
Tolerance
Fagaceae
Gene expression
Castanea sativa
L-Lactate dehydrogenase
Stress
Stem
Complementary DNA
Gene
Dicotyledones
Angiospermae
Heat shock protein
Spermatophyta
Oxidoreductases
Low temperature
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content type line 23
Corresponding author; e-mail lgomez@montes.upm.es; fax 34–91–3366387.
Article, publication date, and citation information can be found at www.plantphysiol.org/cgi/doi/10.1104/pp.103.035857.
Present address: Departamento de Silvicultura, Facultad de Ciencias Forestales, Universidad de Chile, Santiago, Chile.
This work was supported by Plan Nacional de Biotecnología, Ministerio de Ciencia y Tecnología, Spain (grant no. BIO99–0931) and by Comunidad Autónoma de Madrid (grant no. 07M/0047/2000).
Present address: Centro de Investigación Forestal-CIFOR, Instituto Nacional de Investigaciones Agrarias, Ministerio de Agricultura, Pesca y Alimentación, E–28040 Madrid, Spain.
Present address: Facultad de Ciencias, Centro de Biología Molecular Severo Ochoa, Universidad Autónoma de Madrid, E–28049 Madrid, Spain.
OpenAccessLink https://academic.oup.com/plphys/article-pdf/134/4/1708/38702349/plphys_v134_4_1708.pdf
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Snippet Heat shock, and other stresses that cause protein misfolding and aggregation, trigger the accumulation of heat shock proteins (HSPs) in virtually all...
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SubjectTerms Acclimatization
Acclimatization - genetics
Acclimatization - physiology
Agricultural and forest climatology and meteorology. Irrigation. Drainage
Agricultural and forest meteorology
Agronomy. Soil science and plant productions
Amino Acid Sequence
amino acid sequences
Analytical, structural and metabolic biochemistry
Binding and carrier proteins
bioaccumulation
Biological and medical sciences
Castanea sativa
Cell biochemistry
Cell physiology
chemistry
chestnuts
Climatic adaptation. Acclimatization
Cloning, Molecular
cold
cold stress
Complementary DNA
cytosol
DNA, Complementary
DNA, Complementary - chemistry
DNA, Complementary - genetics
Environmental Stress and Adaptation
enzyme activity
Fagaceae
Fagaceae - genetics
Fagaceae - metabolism
Fagaceae - physiology
Freezing
Fundamental and applied biological sciences. Psychology
gene expression regulation
Gene Expression Regulation, Plant
General agronomy. Plant production
genetics
Heat-Shock Proteins
Heat-Shock Proteins - genetics
Heat-Shock Proteins - metabolism
lactate dehydrogenase
Low temperature
messenger RNA
Metabolism
Molecular Sequence Data
Nitrogen metabolism
nucleotide sequences
physiology
Plant physiology and development
plant proteins
Plant Proteins - genetics
Plant Proteins - metabolism
plant response
Plant Stems
Plant Stems - genetics
Plant Stems - metabolism
Plant Stems - physiology
Plants
Proteins
RNA
RNA, Messenger
RNA, Messenger - genetics
RNA, Messenger - metabolism
seasonal variation
Seedlings
Sequence Analysis, DNA
Small heat shock proteins
Stems
Temperature
Title Protein Cryoprotective Activity of a Cytosolic Small Heat Shock Protein That Accumulates Constitutively in Chestnut Stems and Is Up-Regulated by Low and High Temperatures
URI https://www.jstor.org/stable/4281703
https://www.ncbi.nlm.nih.gov/pubmed/15064380
https://www.proquest.com/docview/49160580
https://www.proquest.com/docview/71826997
https://pubmed.ncbi.nlm.nih.gov/PMC419844
Volume 134
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