Preservation of Solanum pimpinellifolium genomic fragments in recombinant genotypes improved the fruit quality of tomato

Five recombinant inbred lines obtained from the F₂ generation of an interspecific cross between cultivar, Caimanta (Cai, Solanum lycopersicum) and wild accession, LA722 (P, S. pimpinellifolium) were crossed to obtain the second cycle hybrids (SCH). Eleven fruit quality traits were assessed in evaluating phenotypic variability among genotypes P, Cai, F₁ (Cai × P), five RILs, and 10 SCH. One of the five recombinant inbred lines and three SCH had higher values than P, as the best genotype for shelf life. Sequence-related amplified polymorphism was used as the molecular method for detecting polymorphism among these 18 genotypes. The percentage of polymorphism in RILs and SCH was 61% and 66% respectively. Moreover, some bands detected in P were present in SCH. Several multivariate analyses were performed to find agreement between the phenotypic variability observed for fruit quality traits and the polymorphism obtained from sequence-related amplified polymorphism markers. A general Procrustes analysis estimated that there was a consensus proportion of 75% between phenotypic and molecular data. There was considerable preservation of some bands from the wild genotype, which could increase the variability in fruit quality traits in populations where the genetic diversity is limited.     

Mesophyll cells of C4 plants have fewer chloroplasts than those of closely related C3 plants

The evolution of C₄ photosynthesis from C₃ ancestors eliminates ribulose bisphosphate carboxylation in the mesophyll (M) cell chloroplast while activating phosphoenolpyruvate (PEP) carboxylation in the cytosol. These changes may lead to fewer chloroplasts and different chloroplast positioning within M cells. To evaluate these possibilities, we compared chloroplast number, size and position in M cells of closely related C₃, C₃–C₄ intermediate and C₄ species from 12 lineages of C₄ evolution. All C₃ species had more chloroplasts per M cell area than their C₄ relatives in high‐light growth conditions. C₃ species also had higher chloroplast coverage of the M cell periphery than C₄ species, particularly opposite intercellular air spaces. In M cells from 10 of the 12 C₄ lineages, a greater fraction of the chloroplast envelope was pulled away from the plasmalemma in the C₄ species than their C₃ relatives. C₃–C₄ intermediate species generally exhibited similar patterns as their C₃ relatives. We interpret these results to reflect adaptive shifts that facilitate efficient C₄ function by enhancing diffusive access to the site of primary carbon fixation in the cytosol. Fewer chloroplasts in C₄ M cells would also reduce shading of the bundle sheath chloroplasts, which also generate energy required by C₄ photosynthesis.     

Phenotypic and molecular characterization of selected tomato recombinant inbred lines derived from the cross <Emphasis Type="Italic">Solanum lycopersicum</Emphasis> × <Emphasis Type="Italic">S. pimpinellifolium</Emphasis>

An important trait defining fresh tomato marketability is fruit shelf life. Exotic germplasm of Solanum pimpinellifolium is able to prolong shelf life. Sixteen recombinant inbred lines with differing values of shelf life and fruit weight were derived by antagonistic-divergent selection from an interspecific cross involving Solanum pimpinellifolium. The objective of this study was to evaluate these recombinant inbred lines for many fruit quality traits such as diameter, height, size, acidity, colour, firmness, shelf life and weight, and to characterize them by amplified fragment length polymorphism markers. For most traits, a wide range of genetic variability was found and a wide range of molecular variation was also detected. Both sets of data allowed the identification of recombinant inbred lines by means of cluster analysis and principal component analysis. Genetic association among some amplified fragment length polymorphism markers and fruit quality traits, suggested by the principal component analysis, could be identified by single point analysis. Potential molecular markers underlying agronomical traits were detected in these recombinant inbred lines.