Bulle Mallesham, Venkatapuram Ajay Kumar, Abbagani Sadanandam, Kirti P B
Agri Biotech Foundation, PJTS Agricultural University Campus, Rajendranagar, Hyderabad 500030, Telangana, India.
International Centre for Genetic Engineering and Biotechnology (ICGEB), Aruna Asaf Ali Marg, New Delhi 110067, India.
J Genet Eng Biotechnol. 2024 Jun;22(2):100380. doi: 10.1016/j.jgeb.2024.100380. Epub 2024 Apr 30.
An effective CRISPR/Cas9 reagent delivery system has been developed in a commercially significant crop, the chilli pepper using a construct harboring two distinct gRNAs targeting exons 14 and 15 of the Phytoene desaturase (CaPDS) gene, whose loss-of-function mutation causes a photo-bleaching phenotype and impairs the biosynthesis of carotenoids. The construct carrying two sgRNAs was observed to create visible albino phenotypes in cotyledons regenerating on a medium containing 80 mg/L kanamycin, and plants regenerated therefrom after biolistic-mediated transfer of CRISPR/Cas9 reagents into chilli pepper cells. Analysis of CRISPR/Cas9 genome-editing events, including kanamycin screening of mutants and assessing homozygosity using the T7 endonuclease assay (T7E1), revealed 62.5 % of transformed plants exhibited successful editing at the target region and displayed both albino and mosaic phenotypes. Interestingly, the sequence analysis showed that insertions and substitutions were present in all the plant lines in the targeted CaPDS region. The detected mutations were mostly 12- to 24-bp deletions that disrupted the exon-intron junction, along with base substitutions and the insertion of 1-bp at the protospacer adjacent motif (PAM) region of the target site. The reduction in essential photosynthetic pigments (chlorophyll a, chlorophyll b and carotenoid) in knockout chilli pepper lines provided further evidence that the CaPDS gene had been functionally disrupted. In this present study, we report that the biolistic delivery of CRISPR/Cas9 reagents into chilli peppers is very effective and produces multiple mutation events in a short span of time.
利用携带两个靶向八氢番茄红素去饱和酶(CaPDS)基因第14和15外显子的不同gRNA构建体,在具有商业价值的作物辣椒中开发了一种有效的CRISPR/Cas9试剂递送系统,该基因功能丧失突变会导致光漂白表型并损害类胡萝卜素的生物合成。观察到携带两个sgRNA的构建体在含有80mg/L卡那霉素的培养基上再生的子叶中产生可见的白化表型,并且在通过生物弹道介导将CRISPR/Cas9试剂转移到辣椒细胞后从中再生出植株。对CRISPR/Cas9基因组编辑事件的分析,包括对突变体进行卡那霉素筛选和使用T7核酸内切酶检测(T7E1)评估纯合性,结果显示62.5%的转化植株在靶区域成功编辑并表现出白化和镶嵌表型。有趣的是,序列分析表明在所有植物系的靶向CaPDS区域中存在插入和替换。检测到的突变大多是12至24bp的缺失,这些缺失破坏了外显子 - 内含子连接,同时还有碱基替换以及在靶位点的原间隔相邻基序(PAM)区域插入1bp。敲除辣椒品系中必需光合色素(叶绿素a、叶绿素b和类胡萝卜素)的减少进一步证明CaPDS基因已被功能性破坏。在本研究中,我们报告将CRISPR/Cas9试剂通过生物弹道递送至辣椒中非常有效,并且能在短时间内产生多个突变事件。