Gaete-Eastman Carlos, Stappung Yazmina, Molinett Sebastián, Urbina Daniela, Moya-Leon María Alejandra, Herrera Raúl
Laboratorio de Fisiología Vegetal y Genética Molecular, Instituto de Ciencias Biológicas, Universidad de Talca, Talca, Chile.
Front Plant Sci. 2022 Sep 20;13:976901. doi: 10.3389/fpls.2022.976901. eCollection 2022.
(Chilean strawberry) is a native species that produces fruit with an exotic pinkish color and a fruity aroma. It has a non-climacteric pattern of fruit ripening, and it is the mother of the commercial x . The ripening of fruit seems stimulated by ABA, and a complete set of genes participate in its softening, color, and aroma development. In addition, a set of transcription factors regulate the entire process, but few of them have been described. Over the last two decades, RNA-seq was used to identify genes at three fruit development/ripening stages, named C2 (unripe, large green) to C4 (full ripe), in whole fruit and fruit without achenes. A total of 204,754 contigs were assembled considering all samples, obtaining an N50 of 1.125 bp. Differentially expressed genes (DEGs) between two samples were identified, obtaining a total of 77,181 DEGs. Transcripts for genes involved in ABA biosynthesis present high and differential expression during the C2, C3, and C4 stages. Besides, contigs corresponding to ABA receptors, which interact with a regulatory network, are also differentially expressed. Genes associated with cell wall remodeling and those involved in flavonoid synthesis were also differentially expressed. An interaction network was built considering differentially expressed genes for the phenylpropanoid and flavonoid molecular pathways and having FcMYB1 as a transcription factor regulator. Identifying key genes could give an option to control the ripening of this non-climacteric fruit.
智利草莓是一种本土物种,其果实呈奇异的粉红色,具有果香。它具有非跃变型果实成熟模式,是商业品种x的母本。果实成熟似乎受脱落酸(ABA)刺激,一组完整的基因参与其软化、颜色和香气的形成。此外,一组转录因子调控整个过程,但其中很少有被描述的。在过去二十年中,RNA测序被用于鉴定全果和无子瘦果果实三个果实发育/成熟阶段(命名为C2,未成熟,大绿色,至C4,完全成熟)的基因。考虑所有样本共组装了204,754个重叠群,N50为1125碱基对。鉴定了两个样本之间的差异表达基因(DEG),共获得77,181个DEG。参与ABA生物合成的基因转录本在C2、C3和C4阶段呈现高表达且差异表达。此外,与ABA受体对应的重叠群也差异表达,ABA受体与调控网络相互作用。与细胞壁重塑相关的基因以及参与类黄酮合成的基因也差异表达。构建了一个相互作用网络,考虑了苯丙烷类和类黄酮分子途径的差异表达基因,并以FcMYB1作为转录因子调控因子。鉴定关键基因可能为控制这种非跃变型果实的成熟提供一种选择。