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Navarro, T.

Publications and source records attributed to Navarro, T..

4 recordsLinked to original sources

Diploid potato lines for the study and improvement of starch metabolism and structure

Diploid potato breeding enables faster genetic improvement via selection against deleterious alleles in inbred lines, unlike breeding by intercrossing tetraploid varieties. Starch is the major source of calories in potato tubers, but the starch properties of diploid lines have rarely been reported. In this study, we provide a comprehensive characterisation of tuber and starch properties in two diploid lines that are early isolates from the Solynta breeding program, B26 and B100, and their F1 hybrids. B100 produced fewer, but larger tubers compared to B26, and both diploid lines produced tubers that are smaller than the tetraploid variety, Clearwater Russet. The low tuber yield of B100 correlates with its high self-compatibility and fruit production. Pruning of fruits in B100 significantly increased total tuber yield per plant by stimulating more tuber initiations, but had no effect on average tuber weight, starch content or starch structure. Among the diploid, hybrid and tetraploid lines examined, there were no differences in the total starch content of tubers. Although amylopectin structure and amylose content were similar between the two diploid lines and the tetraploid comparison, B26 had elevated levels of resistant starch and a striking elongated granule morphology. Our results showcase the variation in source-sink relations and starch structure in diploid potato breeding material, demonstrating their potential for research into the genetics underpinning metabolic and quality traits.

plant biology↗

Expanding the fly eye gene regulatory network: from Drosophila to the hoverfly Episyrphus balteatus.

Comparing developmental mechanisms across long evolutionary distances is challenging, especially when the level of description in the compared species is very disparate. This is the case for the gene regulatory network (GRN) that underlies the development of compound eyes in insects, where the very detailed level description of the network in the fruit fly Drosophila melanogaster contrasts with the knowledge of the network in other well studied insects, such as the flour beetle Tribolium or the desert locust Schistocerca. It is not even known to what extent the Drosophila eye GRN is typical of flies (diptera). Here we have introduced the marmalade fly Episyrphus balteatus (Syrphidae), separated from Drosophila approximately 90 MYrs, as a fly species to compare the mechanisms of compound eye development. The Episyrphus eye develops from an imaginal disc which is, in the overall, similar to that of Drosophila. By generating parallel data sets in Episyrphus and Drosophila to maximize comparability, our results show how the genes known to participate in the early specification of the Drosophila eye and the onset of its differentiation are likely participating in the eye GRN of Episyrphus, further expanding the set of conserved genes/nodes in this network. This gene set might be the basis for further explorations of the developmental mechanisms involved in compound eye development beyond flies. By combining RNAseq and ATACseq profiling with TF motifs we derive the first eye GRN in Episyrphus. When built using Episyrphus/Drosophila conserved nodes, the resulting GRN model exhibited abundant internal connectivity, suggesting that, as proposed in Drosophila, the GRN is knitted with many regulatory feedbacks. Using link conservation as a criterion for discovering new regulatory interactions, we find that the AML1/Runx transcription factor lozenge (lz) is a negative regulator of the retinal determination gene dachshund (dac) in Drosophila. However, although many of the predicted regulatory links are conserved, a large number of regulatory connections seem species-specific, even among conserved nodes. This suggests quite a significant regulatory rewiring during the 90Myr period separating Episyrphus and Drosophila.

developmental biology↗

Feedback control of organ size precision is mediated by BMP2-regulated apoptosis in the Drosophila eye

Biological processes are intrinsically noisy and yet, the result of development -like the species-specific size and shape of organs- is usually remarkably precise. This precision suggests the existence of mechanisms of feedback control that ensure that deviations from a target size are minimized. Still, we have very limited understanding of how these mechanisms operate. Here, we investigate the problem of organ size precision using the Drosophila eye. The size of the adult eye depends on the rates at which eye progenitor cells grow and differentiate. We first find that the progenitor net growth rate results from the balance between their proliferation and apoptosis, with this latter contributing to determining both final eye size and its variability. In turn, apoptosis of progenitor cells is hampered by Dpp, a BMP2/4 signaling molecule transiently produced by early differentiating retinal cells. Our genetic and computational experiments show how the status of retinal differentiation is communicated to progenitors through the differentiation-dependent production of Dpp which, by adjusting the rate of apoptosis, exerts a feedback control over the net growth of progenitors to reduce final eye size variability.

developmental biology↗

Dynamic Hh signaling can generate temporal information during tissue patterning

The differentiation of tissues and organs requires that cells exchange information in space and time. Spatial information is often conveyed by morphogens, molecules that disperse across receiving cells generating signaling gradients. Cells translate such concentration gradients into space-dependent patterns of gene expression and cellular behavior [1, 2]. But could morphogen gradients also convey developmental time? Here, investigating the developmental role of Hh on a component of the Drosophila visual system, the ocellar retina, we discovered that ocellar cells use the non-linear gradient of Hh as a temporal cue, collectively performing the biological equivalent of a mathematical logarithmic transformation. In this way, a morphogen diffusing from a non-moving source is decoded as a wave of differentiating photoreceptors that travels at constant speed throughout the retinal epithelium.

developmental biology↗