Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture and Rural Affairs, Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, Wuhan 430062, China.
College of Life Science and Technology, Huazhong Agricultural University, Wuhan 430070, China.
Int J Mol Sci. 2023 Dec 22;25(1):174. doi: 10.3390/ijms25010174.
The genome-wide long hairpin RNA interference (lhRNAi) library is an important resource for plant gene function research. Molecularly characterizing lhRNAi mutant lines is crucial for identifying candidate genes associated with corresponding phenotypes. In this study, a dwarf and sterile line named P198 was screened from the () RNAi library. Three different methods confirmed that eight copies of T-DNA are present in the P198 genome. However, only four insertion positions were identified in three chromosomes using fusion primer and nested integrated polymerase chain reaction. Therefore, the T-DNA insertion sites and copy number were further investigated using Oxford Nanopore Technologies (ONT) sequencing, and it was found that at least seven copies of T-DNA were inserted into three insertion sites. Based on the obtained T-DNA insertion sites and hairpin RNA (hpRNA) cassette sequences, three candidate genes related to the P198 phenotype were identified. Furthermore, the potential differentially expressed genes and pathways involved in the dwarfism and sterility phenotype of P198 were investigated by RNA-seq. These results demonstrate the advantage of applying ONT sequencing to investigate the molecular characteristics of transgenic lines and expand our understanding of the complex molecular mechanism of dwarfism and male sterility in .
全基因组长发夹 RNA 干扰 (lhRNAi) 文库是植物基因功能研究的重要资源。对 lhRNAi 突变体进行分子特征分析对于鉴定与相应表型相关的候选基因至关重要。本研究从 () RNAi 文库中筛选出一个矮化不育株系 P198。三种不同的方法证实 P198 基因组中存在 8 个拷贝的 T-DNA。然而,使用融合引物和嵌套整合聚合酶链反应仅在三条染色体上鉴定出四个插入位置。因此,使用 Oxford Nanopore Technologies (ONT) 测序进一步研究了 T-DNA 插入位点和拷贝数,发现至少有 7 个拷贝的 T-DNA 插入到三个插入位点。基于获得的 T-DNA 插入位点和发夹 RNA (hpRNA) 盒序列,鉴定出与 P198 表型相关的三个候选基因。此外,通过 RNA-seq 研究了 P198 矮化不育表型涉及的潜在差异表达基因和途径。这些结果表明,应用 ONT 测序来研究转基因株系的分子特征具有优势,并扩展了我们对矮化和雄性不育复杂分子机制的理解。