Malaysian Agricultural Research and Development Institute (MARDI), P.O. Box 12301, Kuala Lumpur 50774, Malaysia.
Department of Microbiology, Faculty of Biotechnology & Biomolecular Sciences, Universiti Putra Malaysia, UPM Serdang 43400, Selangor Darul Ehsan, Malaysia.
Molecules. 2014 Jun 19;19(6):8350-62. doi: 10.3390/molecules19068350.
The purpose of this study was to evaluate the effectiveness of using RNA interference in down regulating the expression of 1-aminocyclopropane-1-carboxylic acid oxidase gene in Eksotika papaya. One-month old embryogenic calli were separately transformed with Agrobacterium strain LBA 4404 harbouring the three different RNAi pOpOff2 constructs bearing the 1-aminocyclopropane-1-carboxylic acid oxidase gene. A total of 176 putative transformed lines were produced from 15,000 calli transformed, selected, then regenerated on medium supplemented with kanamycin. Integration and expression of the targeted gene in putatively transformed lines were verified by PCR and real-time RT-PCR. Confined field evaluation of a total of 31 putative transgenic lines planted showed a knockdown expression of the targeted ACO1 and ACO2 genes in 13 lines, which required more than 8 days to achieve the full yellow colour (Index 6). Fruits harvested from lines pRNAiACO2 L2-9 and pRNAiACO1 L2 exhibited about 20 and 14 days extended post-harvest shelf life to reach Index 6, respectively. The total soluble solids contents of the fruits ranged from 11 to 14° Brix, a range similar to fruits from non-transformed, wild type seed-derived plants.
本研究旨在评估 RNA 干扰在下调 Eksotika 木瓜中 1-氨基环丙烷-1-羧酸氧化酶基因表达方面的有效性。将 1 个月大的胚性愈伤组织分别用携带三个不同的 RNAi pOpOff2 构建体的农杆菌菌株 LBA 4404 转化,这些构建体携带 1-氨基环丙烷-1-羧酸氧化酶基因。从转化的 15000 个愈伤组织中产生了总共 176 个假定转化系,经过选择后在含有卡那霉素的培养基上再生。通过 PCR 和实时 RT-PCR 验证了目标基因在假定转化系中的整合和表达。对总共 31 个假定转基因系进行的田间评估表明,在 13 个系中,靶标 ACO1 和 ACO2 基因的表达被下调,这些系需要超过 8 天才能达到完全黄色(指数 6)。从 pRNAiACO2 L2-9 和 pRNAiACO1 L2 系收获的果实分别延长了约 20 天和 14 天的采后货架期,达到指数 6。果实的总可溶性固形物含量范围为 11 至 14°Brix,与非转化的、野生型种子衍生植株的果实相似。