Abstract:Ripening of climacteric fruits is a complex physiological phenomenon, which makes berries attractive/palatable and also determines their nutritional characteristics. We report here a comparative proteomic investigation on tomato fruits from a regional and commercial elite ecotype during maturation. Several hundreds of protein components were resolved on 2-DE gels (pH range 4-7) stained with colloidal Coomassie; almost 57% presented overlapping gel coordinates between the two compared varieties. Specific protei… Show more
“…The mechanisms governing the differentiation of plastids such as the conversion of proplastids to chloroplasts or chloroplasts to chromoplasts have received little attention and are barely mentioned in recent reviews on plastid proteomics (Armbruster et al, 2011;van Wijk and Baginsky, 2011). The pattern of changes in protein abundance reported here is in agreement with proteomic data generated in whole fruit by others (Rocco et al, 2006;Faurobert et al, 2007). The western blots of six proteins representative of several metabolic or regulatory pathways give a pattern of changes that is similar to proteomic analysis.…”
Section: Proteins Involved In Energy Provision and Translocation Actisupporting
confidence: 78%
“…Forty-seven proteins have been identified both in the plastid proteome described in this work and in the whole fruit proteome of Rocco et al (2006) and Faurobert et al (2007). Although the tomato varieties and the quantification methods were very different, the ratios of abundance between the three stages of plastid development (MG, B, and R) were identical or similar, thus confirming the accuracy of the quantification methods.…”
Section: Proteomic Specificities Of the Three Stages Of Plastid Diffementioning
confidence: 49%
“…Proteomic data on the whole tomato fruit are available in which quantitative data on plastidial proteins can be encountered (Rocco et al, 2006;Faurobert et al, 2007). Forty-seven proteins have been identified both in the plastid proteome described in this work and in the whole fruit proteome of Rocco et al (2006) and Faurobert et al (2007).…”
Section: Proteomic Specificities Of the Three Stages Of Plastid Diffementioning
confidence: 99%
“…Another signal peptidase, plastidic signal peptidase (PLSP1, Solyc12g007120) involved in thylakoid development through its involvement in processing the Toc75 envelope protein and 0E33 thylakoid luminal protein (Shipman-Roston et al, 2010) was absent at the R stage, which is consistent with thylakoid dismantling. (Schauer et al, 2006;Deborde et al, 2009;Moing et al, 2011), proteomics (Rocco et al, 2006;Faurobert et al, 2007;Palma et al, 2011), and more recently, a combination of all of them . However these technologies have been scarcely used in the study of subcellular organelles such as chromoplasts.…”
Section: Proteins Involved In Energy Provision and Translocation Actimentioning
A comparative proteomic approach was performed to identify differentially expressed proteins in plastids at three stages of tomato (Solanum lycopersicum) fruit ripening (mature-green, breaker, red). Stringent curation and processing of the data from three independent replicates identified 1,932 proteins among which 1,529 were quantified by spectral counting. The quantification procedures have been subsequently validated by immunoblot analysis of six proteins representative of distinct metabolic or regulatory pathways. Among the main features of the chloroplast-to-chromoplast transition revealed by the study, chromoplastogenesis appears to be associated with major metabolic shifts: (1) strong decrease in abundance of proteins of light reactions (photosynthesis, Calvin cycle, photorespiration) and carbohydrate metabolism (starch synthesis/degradation), mostly between breaker and red stages and (2) increase in terpenoid biosynthesis (including carotenoids) and stress-response proteins (ascorbate-glutathione cycle, abiotic stress, redox, heat shock). These metabolic shifts are preceded by the accumulation of plastid-encoded acetyl Coenzyme A carboxylase D proteins accounting for the generation of a storage matrix that will accumulate carotenoids. Of particular note is the high abundance of proteins involved in providing energy and in metabolites import. Structural differentiation of the chromoplast is characterized by a sharp and continuous decrease of thylakoid proteins whereas envelope and stroma proteins remain remarkably stable. This is coincident with the disruption of the machinery for thylakoids and photosystem biogenesis (vesicular trafficking, provision of material for thylakoid biosynthesis, photosystems assembly) and the loss of the plastid division machinery. Altogether, the data provide new insights on the chromoplast differentiation process while enriching our knowledge of the plant plastid proteome.
“…The mechanisms governing the differentiation of plastids such as the conversion of proplastids to chloroplasts or chloroplasts to chromoplasts have received little attention and are barely mentioned in recent reviews on plastid proteomics (Armbruster et al, 2011;van Wijk and Baginsky, 2011). The pattern of changes in protein abundance reported here is in agreement with proteomic data generated in whole fruit by others (Rocco et al, 2006;Faurobert et al, 2007). The western blots of six proteins representative of several metabolic or regulatory pathways give a pattern of changes that is similar to proteomic analysis.…”
Section: Proteins Involved In Energy Provision and Translocation Actisupporting
confidence: 78%
“…Forty-seven proteins have been identified both in the plastid proteome described in this work and in the whole fruit proteome of Rocco et al (2006) and Faurobert et al (2007). Although the tomato varieties and the quantification methods were very different, the ratios of abundance between the three stages of plastid development (MG, B, and R) were identical or similar, thus confirming the accuracy of the quantification methods.…”
Section: Proteomic Specificities Of the Three Stages Of Plastid Diffementioning
confidence: 49%
“…Proteomic data on the whole tomato fruit are available in which quantitative data on plastidial proteins can be encountered (Rocco et al, 2006;Faurobert et al, 2007). Forty-seven proteins have been identified both in the plastid proteome described in this work and in the whole fruit proteome of Rocco et al (2006) and Faurobert et al (2007).…”
Section: Proteomic Specificities Of the Three Stages Of Plastid Diffementioning
confidence: 99%
“…Another signal peptidase, plastidic signal peptidase (PLSP1, Solyc12g007120) involved in thylakoid development through its involvement in processing the Toc75 envelope protein and 0E33 thylakoid luminal protein (Shipman-Roston et al, 2010) was absent at the R stage, which is consistent with thylakoid dismantling. (Schauer et al, 2006;Deborde et al, 2009;Moing et al, 2011), proteomics (Rocco et al, 2006;Faurobert et al, 2007;Palma et al, 2011), and more recently, a combination of all of them . However these technologies have been scarcely used in the study of subcellular organelles such as chromoplasts.…”
Section: Proteins Involved In Energy Provision and Translocation Actimentioning
A comparative proteomic approach was performed to identify differentially expressed proteins in plastids at three stages of tomato (Solanum lycopersicum) fruit ripening (mature-green, breaker, red). Stringent curation and processing of the data from three independent replicates identified 1,932 proteins among which 1,529 were quantified by spectral counting. The quantification procedures have been subsequently validated by immunoblot analysis of six proteins representative of distinct metabolic or regulatory pathways. Among the main features of the chloroplast-to-chromoplast transition revealed by the study, chromoplastogenesis appears to be associated with major metabolic shifts: (1) strong decrease in abundance of proteins of light reactions (photosynthesis, Calvin cycle, photorespiration) and carbohydrate metabolism (starch synthesis/degradation), mostly between breaker and red stages and (2) increase in terpenoid biosynthesis (including carotenoids) and stress-response proteins (ascorbate-glutathione cycle, abiotic stress, redox, heat shock). These metabolic shifts are preceded by the accumulation of plastid-encoded acetyl Coenzyme A carboxylase D proteins accounting for the generation of a storage matrix that will accumulate carotenoids. Of particular note is the high abundance of proteins involved in providing energy and in metabolites import. Structural differentiation of the chromoplast is characterized by a sharp and continuous decrease of thylakoid proteins whereas envelope and stroma proteins remain remarkably stable. This is coincident with the disruption of the machinery for thylakoids and photosystem biogenesis (vesicular trafficking, provision of material for thylakoid biosynthesis, photosystems assembly) and the loss of the plastid division machinery. Altogether, the data provide new insights on the chromoplast differentiation process while enriching our knowledge of the plant plastid proteome.
“…Due to its economic importance, as well as many favorable genetic and agricultural features, it has also become a model species for molecular studies aimed at improving fruit quality (Giovannoni, 2004;Rocco et al, 2006) and resistance toward pathogens (Ercolano et al, 2012). Tomato is affected by over 200 diseases induced by viruses, bacteria, fungi or nematodes (Jones et al, 1991), which are the cause of severe annual yield losses worldwide.…”
a b s t r a c tGrafting can enhance the tolerance of vegetable crops to soilborne diseases. The aim of this study was to investigate whether different tomato scionerootstock combinations may affect the plant susceptibility to Fusarium oxysporum f. sp. radicis-lycopersici (FORL), the causal agent of crown and root rot. A proteomic approach was used to investigate whenever the protein repertoire of the rootstock can be modified by FORL infection, in relation to cultivar susceptibility/tolerance to the disease. To this purpose, plants of tomato hybrids with different vigor, "Costoluto Genovese" (less vigorous) and "Kadima" (more vigorous), were grafted onto "Cuore di Bue" and "Natalia" hybrids, sensitive and tolerant versus FORL infections, respectively. Disease symptoms, plant biomasses, and protein expression patterns were evaluated 45 days after FORL inoculation. The extent of vascular discoloration caused by FORL in tomato plants grafted on "Natalia" rootstock (0.12e0.37 cm) was significantly lower than that of plants grafted on sensitive "Cuore di Bue" (1.75e6.50 cm). FORL symptoms significantly differed between "Costoluto Genovese" and "Kadima" scions only when grafted on sensitive rootstock. Shoot FW of non-inoculated "Kadima"/"Cuore di Bue" combination was 35% lower than "Kadima"/"Natalia", whereas no difference was manifested in inoculated plants. Shoot FW of inoculated "Costoluto Genovese"/"Cuore di Bue" combination was decreased of 39%, whereas that of "Costoluto Genovese"/"Natalia" of 11%, compared to control plants. Proteomic results showed a higher representation of proteins associated with pathogen infection in the tolerant rootstock, compared to the sensitive one, meaning a direct involvement of plant defence mechanisms in the tomato response to the pathogen challenge.
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