Yin Xiangzhen, Zhang Yingxin, Chen Yuhong, Wang Jingqiao, Wang Richard R-C, Fan Chengming, Hu Zanmin
State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Innovation Academy for Seed Design, Chinese Academy of Sciences, Beijing, China.
College of Agriculture, Yangtze University, Jingzhou, China.
Front Plant Sci. 2021 Oct 4;12:743792. doi: 10.3389/fpls.2021.743792. eCollection 2021.
Plant artificial minichromosomes are the next-generation technology for plant genetic engineering and represent an independent platform for expressing foreign genes and the tools for studying the structure and function of chromosomes. Minichromosomes have been successfully produced by telomere-mediated chromosome truncation in several plants. However, previous studies have primarily focused on the construction and rough characterization of minichromosomes, while the development of stably inherited minichromosomes and their precise characterization and tracking over different generations have rarely been demonstrated. In this study, a 0.35-kb direct repeat of the telomeric sequence was transformed into to produce artificial minichromosomes, which were analyzed by multifluorescence hybridization (multi-FISH), Southern hybridization, and primer extension telomere rapid amplification (PETRA). The stably inherited minichromosomes C2 and C4 were developed by crossing transgenic plants with wild-type plants and then selfing the hybrids. Notably, two truncation sites on chromosomes C2 and C4, respectively, were identified by resequencing; thus, the artificial minichromosomes were tracked over different generations with insertion site-specific PCR. This study provided two stably inherited minichromosomes in oilseed rape and describes approaches to precisely characterize the truncation position and track the minichromosomes in offspring through multi-FISH, genome resequencing, and insertion site-specific PCR.
植物人工微型染色体是植物基因工程的下一代技术,代表了一个用于表达外源基因的独立平台以及研究染色体结构和功能的工具。微型染色体已通过端粒介导的染色体截断在几种植物中成功产生。然而,以往的研究主要集中在微型染色体的构建和粗略表征上,而稳定遗传的微型染色体的开发及其在不同世代中的精确表征和追踪则鲜有报道。在本研究中,将0.35 kb的端粒序列直接重复序列转化以产生人工微型染色体,通过多荧光原位杂交(multi-FISH)、Southern杂交和引物延伸端粒快速扩增(PETRA)对其进行分析。通过将转基因植物与野生型植物杂交,然后使杂种自交,开发出了稳定遗传的微型染色体C2和C4。值得注意的是,通过重测序分别鉴定了染色体C2和C4上的两个截断位点;因此,利用插入位点特异性PCR在不同世代中追踪人工微型染色体。本研究在油菜中提供了两个稳定遗传的微型染色体,并描述了通过多荧光原位杂交、基因组重测序和插入位点特异性PCR精确表征截断位置并在后代中追踪微型染色体的方法。