Iglesias Dianella, Donato Capote Marcos de, Méndez Tenorio Alfonso, Valdivia Ana Victoria, Gutiérrez-García Claudia, Paul Sujay, Iqbal Hafiz M N, Villarreal María Luisa, Sharma Ashutosh
Centro de Investigación en Biotecnología, Universidad Autónoma del Estado de Morelos, Cuernavaca 62210, CP, Mexico.
Centre of Bioengineering, NatProLab, School of Engineering and Sciences, Tecnologico de Monterrey, Querétaro 76130, CP, Mexico.
Plants (Basel). 2022 Jul 20;11(14):1879. doi: 10.3390/plants11141879.
spp. is popularly used in Mexican traditional medicine. Some populations of exert anxiolytic and sedative effects due to the presence of the modified triterpenoids galphimines. However, the galphimine synthesis pathway has not yet been elucidated. Hence, in this study, a comparative transcriptome analysis between two contrasting populations of spp., a galphimine-producer, and a non-galphimine-producer, is performed using RNA-Seq in the Illumina Next Seq 550 platform to identify putative candidates genes that encode enzymes of this metabolic pathway. Transcriptome functional annotation was performed using the Blast2GO in levels of gene ontology. For differential expression analysis, edgeR, pheatmap, and Genie3 library were used. To validate transcriptome data, qPCR was conducted. In producer and non-producer plants of both populations of spp., most of the transcripts were grouped in the Molecular Function level of gene ontology. A total of 680 differentially expressed transcripts between producer and non-producer plants were detected. In galphimine-producer plants, a larger number of highly expressed transcripts related to acyclic and polycyclic terpene synthesis were identified. As putative candidate genes involved in the galphimine synthesis pathway, P450 family members and enzymes with kinase activity were identified.
某植物物种在墨西哥传统医学中广泛使用。由于存在修饰的三萜类化合物加尔菲明,该植物的一些种群具有抗焦虑和镇静作用。然而,加尔菲明的合成途径尚未阐明。因此,在本研究中,使用Illumina Next Seq 550平台上的RNA-Seq对该植物物种的两个对比种群(一个加尔菲明生产者和一个非加尔菲明生产者)进行了比较转录组分析,以鉴定编码该代谢途径酶的推定候选基因。使用Blast2GO在基因本体水平上进行转录组功能注释。对于差异表达分析,使用了edgeR、pheatmap和Genie3库。为了验证转录组数据,进行了qPCR。在该植物物种的两个种群的生产者和非生产者植物中,大多数转录本被归类在基因本体的分子功能水平。在生产者和非生产者植物之间共检测到680个差异表达的转录本。在加尔菲明生产者植物中,鉴定出了大量与无环和多环萜烯合成相关的高表达转录本。作为参与加尔菲明合成途径的推定候选基因,鉴定出了细胞色素P450家族成员和具有激酶活性的酶。