Browsing by Author "Núñez Lillo, Gerardo"

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    Fruit sugar hub: gene regulatory network associated with soluble solids content (SSC) in Prunus persica
    (2024) Núñez Lillo, Gerardo; Lillo Carmona, Victoria; Pérez Donoso, Alonso Gastón; Pedreschi, Romina; Campos Vargas, Reinaldo; Meneses Araya, Claudio Antonio
    Chilean peach growers have achieved worldwide recognition for their high-quality fruit products. Among the main factors influencing peach fruit quality, sweetness is pivotal for maintaining the market's competitiveness. Numerous studies have been conducted in different peach-segregating populations to unravel SSC regulation. However, different cultivars may also have distinct genetic conformation, and other factors, such as environmental conditions, can significantly impact SSC. Using a transcriptomic approach with a gene co-expression network analysis, we aimed to identify the regulatory mechanism that controls the sugar accumulation process in an 'O × N' peach population. This population was previously studied through genomic analysis, associating LG5 with the genetic control of the SSC trait. The results obtained in this study allowed us to identify 91 differentially expressed genes located on chromosome 5 of the peach genome as putative new regulators of sugar accumulation in peach, together with a regulatory network that involves genes directly associated with sugar transport (PpSWEET15), cellulose biosynthesis (PpCSLG2), flavonoid biosynthesis (PpPAL1), pectin modifications (PpPG, PpPL and PpPMEi), expansins (PpEXPA1 and PpEXPA8) and several transcription factors (PpC3H67, PpHB7, PpRVE1 and PpCBF4) involved with the SSC phenotype. These results contribute to a better understanding of the genetic control of the SSC trait for future breeding programs in peaches.
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    Sup4h5-L19 activation tagging line partially restores root hair growth in p4h5 mutant by introducing small transcriptomic changes in Arabidopsis thaliana
    (2024) Urzúa Lehuedé, Tomás; Núñez Lillo, Gerardo; Salgado Salter, Juan; Achá, Romina; Ibeas, Miguel Anguel; Meneses Araya, Claudio Antonio; Estévez, José M.
    An specific group of 2-oxoglutarate (2OG) dioxygenases named as Prolyl 4-Hydroxylases (P4H) produce trans-4-hydroxyproline (Hyp/O) from peptidyl-proline, catalyzing proline hydroxylation of cell wall glycoproteins EXT, AGPs, and HRGPs in plant cells, a crucial modification for O-glycosylation. Out of the Arabidopsis thaliana 13 P4Hs, P4H5 regulate root hair cell elongation and T-DNA insertional p4h5 mutant has arrested cell elongation and shortened root hairs. P4H5 selectively hydroxylates EXT proline units indicating that EXT proline hydroxylation as an essential modification for root hair growth. In this work, we isolate an activation-tagging line called Sup4h5-L19/p4h5 (p4h5-L19) that partially suppressed root hair phenotype in the p4h5 mutant background. The T-DNA insertion site was mapped by Thermal Asymmetric Interlaced PCR (TAIL-PCR) followed by PCR product sequencing and the T-DNA is inserted at the beginning of the sixth exon of the AT3G17750 gene, an uncharacterized cytosolic kinase. By analyzing expression changes and mutants analysis in this loci, no clear direct effect was detected. By RNA-seq analysis, it become clear that p4h5-L19 may largely reverse the genetic alterations caused by the p4h5 mutant in Wt Col-0, particularly at 10°C where there is an increase in root hair growth, with a total of 14 genes that have been activated and 83 genes that have been suppressed due to the enhancer of the activation tagging L19 in p4h5 L19 compared to p4h5. Among these genes, 3 of them, Tonoplast Intrinsic Proteins (TIPs), were identified to be root hair specific (TIP1;1, TIP2;2, and TIP2;3) and the corresponding mutants for two of them (TIP1;1 and TIP2;3) showed reduced root hair growth response at low temperature. This study unmasked new components of the root hair growth response at low temperature that works independently of the O-glycosyated EXTs in the cell walls.
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    Two antagonistic gene regulatory networks drive Arabidopsis root hair growth at low temperature linked to a low-nutrient environment
    (WILEY, 2025) Urzúa Lehuede, Tomás; Berdion Gabarain, Victoria; Ibeas, Miguel Angel; Salinas Grenet, Hernán; Achá Escobar, Romina; Moyano, Tomás C.; Ferrero, Lucía; Núñez Lillo, Gerardo; Pérez Díaz, Jorge; Perotti, María Florencia; Natali Miguel, Virginia; Spies, Fiorella Paola; Rosas, Miguel A.; Kawamura, Ayako; Rodríguez García, Diana R.; Kim, Ah-Ram; Nolan, Trevor; Moreno, Adrian A.; Sugimoto, Keiko; Perrimon, Norbert; Sanguinet, Karen A.; Meneses Araya, Claudio Antonio; Chan, Raquel L.; Ariel, Federico; Alvárez, José M.; Estévez, José M.
    Root hair (RH) cells can elongate to several hundred times their initial size, and are an ideal model system for investigating cell size control. Their development is influenced by both endogenous and external signals, which are combined to form an integrative response. Surprisingly, a low-temperature condition of 10 degrees C causes increased RH growth in Arabidopsis and in several monocots, even when the development of the rest of the plant is halted. Previously, we demonstrated a strong correlation between RH growth response and a significant decrease in nutrient availability in the growth medium under low-temperature conditions. However, the molecular basis responsible for receiving and transmitting signals related to the availability of nutrients in the soil, and their relation to plant development, remain largely unknown. We have discovered two antagonic gene regulatory networks (GRNs) controlling RH early transcriptome responses to low temperature. One GNR enhances RH growth and it is commanded by the transcription factors (TFs) ROOT HAIR DEFECTIVE 6 (RHD6), HAIR DEFECTIVE 6-LIKE 2 and 4 (RSL2-RSL4) and a member of the homeodomain leucine zipper (HD-Zip I) group I 16 (AtHB16). On the other hand, a second GRN was identified as a negative regulator of RH growth at low temperature and it is composed by the trihelix TF GT2-LIKE1 (GTL1) and the associated DF1, a previously unidentified MYB-like TF (AT2G01060) and several members of HD-Zip I group (AtHB3, AtHB13, AtHB20, AtHB23). Functional analysis of both GRNs highlights a complex regulation of RH growth response to low temperature, and more importantly, these discoveries enhance our comprehension of how plants synchronize RH growth in response to variations in temperature at the cellular level.