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Gimeno-Paez, E.

Publications and source records attributed to Gimeno-Paez, E..

2 recordsLinked to original sources

Characterization of a dominant SmNac-like gene as a candidate for photosensitivity in the fruit peel of eggplant

Anthocyanins in the fruit peel of photosensitive eggplants exhibit a different distribution pattern compared to the photo-insensitive ones. The latter exhibits a uniform anthocyanin content, whereas photosensitive eggplants lack anthocyanin accumulation in areas not exposed to light, such as under the calyx, or have lower concentrations in less-exposed areas. In the current research work, genetic analysis of F1 and F2 populations revealed that the photo-insensitive phenotype in eggplants follows an autosomal dominant inheritance with a 3:1 ratio, indicating that the photosensitive trait is regulated by a single dominant gene. To locate and narrow down the genomic region underlying photosensitivity, a segregating F2 population was used for bulked segregant analysis sequencing (BSA-seq) and compared with previous QTLs identified in previous developed eggplants populations (ILs and MAGIC population). The accumulation of QTLs at the end of chromosome 10 postulate that chromose region as a hot spot for anthocyanin related traits. In our population all the QTLs considered overlap between the genomic region 84,1-87,9 Mb. Moreover, no DNA mutations in the progenitors of the eggplant accessions used were found. A RNA-seq analysis of bagged photosensitive and photo- insensitive eggplants was performed, as a result we identified the SmNAC1-like protein gene as a promising gene to be involved in fruit photosensitivity trait. In the photo-insensitive accession (IVIA- 371) SmNAC1-like protein was depply repressed compare to the photosensitive accession (ASI-S-1). No consistent mutations in the coding sequences (CDS) of SmNac-like protein locus among all the different eggplants accessions used were found, suggesting that other layer of regulation maybe acting in our eggplant accessions. These findings provide new insight into the regulation of the molecular mechanisms of anthocyanin biosynthesis in eggplant as point out for the first time the possible role of NAC transcription factors in the anthocyanin biosynthesis in eggplant.

plant biology↗

Agronomic treatments combined with embryo rescue for rapid generation advancement in tomato speed breeding

Unlike other major crops, little research has been performed on tomato for reducing generation time for speed breeding. We evaluated several agronomic treatments for reducing the generation time of tomato in the M82 (determinate) and Moneymaker (indeterminate) varieties and evaluated the best combination in conjunction with embryo rescue. In a first experiment under the autumn cycle, five container sizes, from 0.2 1 (XS) to 6 1 (XL), were evaluated. We found that plants from the XL containers exhibited better development and required less time from sowing to anthesis (DSA) and for anthesis to fruit ripening (DAR). In a second experiment, using XL containers in the autumn-winter cycle, we evaluated cold priming at the cotyledonary stage, water stress, P supplementation, and K supplementation on generation time. We found that, compared to the control, cold priming significantly reduced the number of leaves and plant height to first inflorescence as well as DSA (2.7 d), while K supplementation reduced DAR (8.8 d). No effects of these treatments were observed for other growth of physiological traits. In a third experiment with XL containers in the spring-summer cycle, the combination of cold priming plus K supplementation was tested, confirming the significant effect of the combination on generation time (2.9 d for DSA and 3.9 d for DAR). Embryo rescue during the cell expansion cycle (average of 22.0 d and 23.3 d after anthesis for M82 and Moneymaker, respectively) allowed shortening the generation time by 8.7 d in M82 and 11.6 d in Moneymaker compared to the in planta fruit ripening. The combination of agronomic treatments with embryo rescue can make an effective contribution to increase the number of generations per year for speed breeding in tomato from the current three to four.

plant biology↗