Department of Botany, College of Life Sciences, Hunan Normal University, Changsha, 410081, China.
CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan, 430074, China.
BMC Genomics. 2024 Apr 1;25(1):322. doi: 10.1186/s12864-024-10247-9.
Primulina hunanensis, a troglobitic plant within the Primulina genus of Gesneriaceae family, exhibits robust resilience to arid conditions and holds great horticultural potential as an ornamental plant. The work of chloroplast genome (cpDNA) has been recently accomplished, however, the mitochondrial genome (mtDNA) that is crucial for plant evolution has not been reported.
In this study, we sequenced and assembled the P. hunanensis complete mtDNA, and elucidated its evolutionary and phylogenetic relationships. The assembled mtDNA spans 575,242 bp with 43.54% GC content, encompassing 60 genes, including 37 protein-coding genes (PCGs), 20 tRNA genes, and 3 rRNA genes. Notably, high number of repetitive sequences in the mtDNA and substantial sequence translocation from chloroplasts to mitochondria were observed. To determine the evolutionary and taxonomic positioning of P. hunanensis, a phylogenetic tree was constructed using mitochondrial PCGs from P. hunanensis and 32 other taxa. Furthermore, an exploration of PCGs relative synonymous codon usage, identification of RNA editing events, and an investigation of collinearity with closely related species were conducted.
This study reports the initial assembly and annotation of P. hunanensis mtDNA, contributing to the limited mtDNA repository for Gesneriaceae plants and advancing our understanding of their evolution for improved utilization and conservation.
湖南省报春苣苔(Primulina hunanensis)是苦苣苔科报春苣苔属的一种地下生植物,具有很强的耐旱能力,具有很大的园艺观赏潜力。叶绿体基因组(cpDNA)的工作最近已经完成,然而,对于植物进化至关重要的线粒体基因组(mtDNA)尚未报道。
在本研究中,我们对 P. hunanensis 的完整 mtDNA 进行了测序和组装,并阐明了其进化和系统发育关系。组装的 mtDNA 跨度为 575,242 bp,GC 含量为 43.54%,包含 60 个基因,包括 37 个蛋白质编码基因(PCGs)、20 个 tRNA 基因和 3 个 rRNA 基因。值得注意的是,mtDNA 中存在大量的重复序列,并且大量的序列从叶绿体转移到线粒体。为了确定 P. hunanensis 的进化和分类地位,我们使用来自 P. hunanensis 和 32 个其他类群的线粒体 PCGs 构建了系统发育树。此外,我们还研究了 PCGs 的相对同义密码子使用、RNA 编辑事件的鉴定以及与近缘物种的共线性。
本研究报告了 P. hunanensis mtDNA 的初步组装和注释,为苦苣苔科植物有限的 mtDNA 库做出了贡献,并增进了我们对其进化的理解,以促进其更好的利用和保护。