Nishihara Masahiro, Hirabuchi Akiko, Goto Fumina, Watanabe Aiko, Yoshida Chiharu, Washiashi Rie, Odashima Masashi, Nemoto Keiichirou
Iwate Biotechnology Research Center, 22-174-4 Narita, Kitakami, Iwate 024-0003, Japan.
Iwate Agricultural Research Center, 20-1 Narita, Kitakami, Iwate 024-0003, Japan.
Plant Biotechnol (Tokyo). 2023 Sep 25;40(3):229-236. doi: 10.5511/plantbiotechnology.23.0424a.
Japanese cultivated gentians are highly valued ornamental flowers in Japan, but the flower shape is mostly limited to the single-flower type, unlike other flowers such as roses and carnations. To overcome this limitation, we used the CRISPR/Cas9 genome editing system to increase double-flowered genetic resources in gentians. Our approach targeted an () floral homeotic gene (), which is responsible for the natural mutation that causes double flowers in gentians. We designed two targets in exon 1 of for genome editing and found that 9 of 12 herbicide-resistant shoots had biallelic mutations in the target regions of . These nine lines all produced double flowers, with stamens converted into petaloid organs, similar to the natural mutant. We also analyzed the off-target effects of , which is homologous to , and found that such effects occurred in gentian genome editing but with low frequency. Furthermore, we successfully produced transgene-free genome-edited plants (null segregants) by crossing with wild-type pollen. F seedlings were subjected to PCR analysis to determine whether foreign DNA sequences, two partial regions of the CaMV35S promoter and gene, were present in the genome. As a result, foreign genes were segregated at a 1 : 1 ratio, indicating successful null segregant production. Using PCR analysis, we confirmed that four representative null segregants did not contain transfer DNA. In summary, our study demonstrates that the CRISPR/Cas9 system can efficiently produce double-flowered gentians, and null segregants can also be obtained. These genome-edited plants are valuable genetic resources for future gentian breeding programs.
日本栽培的龙胆是日本备受珍视的观赏花卉,但花型大多局限于单花类型,不像玫瑰和康乃馨等其他花卉。为克服这一局限,我们利用CRISPR/Cas9基因组编辑系统增加龙胆的重瓣遗传资源。我们的方法靶向一个()花同源异型基因(),该基因负责导致龙胆重瓣的自然突变。我们在的外显子1中设计了两个用于基因组编辑的靶点,发现12株抗除草剂芽苗中有9株在的靶点区域存在双等位基因突变。这9个株系均产生了重瓣花,雄蕊转化为花瓣状器官,类似于自然突变体。我们还分析了与同源的的脱靶效应,发现这种效应在龙胆基因组编辑中发生,但频率较低。此外,我们通过与野生型花粉杂交成功培育出无转基因的基因组编辑植株(纯合分离株)。对F幼苗进行PCR分析,以确定基因组中是否存在外源DNA序列,即CaMV35S启动子和基因的两个部分区域。结果,外源基因以1:1的比例分离,表明成功产生了纯合分离株。通过PCR分析,我们证实4个代表性的纯合分离株不含转移DNA。总之,我们的研究表明,CRISPR/Cas9系统可以高效培育出重瓣龙胆,并且也能获得纯合分离株。这些基因组编辑植株是未来龙胆育种计划的宝贵遗传资源。