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通过 CRISPR/Cas9 在烟草中鉴定、表征和遗传转化木质素和果胶多糖。

Identification, charectrization and genetic transformation of lignin and pectin polysaccharides through CRISPR/Cas9 in Nicotiana tobacum.

机构信息

Key Laboratory for Tobacco Gene Resources, Tobacco Research Institute, Chinese Academy of Agricultural Sciences, Qingdao, 266101, China.

Regional Agricultural Research Institute, Bahawalpur, 63100, Pakistan.

出版信息

Funct Integr Genomics. 2024 Oct 14;24(5):188. doi: 10.1007/s10142-024-01472-2.

Abstract

CRISPR/Cas9 system has been successfully implemented in animals and plants is a second-generation genome editing tool. We are able to optimize a Cas9 system to edited Ntab06050 and Ntab0857410 genes in HD and K326 tobacco cultivars respectively. The gene Ntab06050 is related to lignin synthesis while the gene Ntab0857410 belongs to pectin synthesis by utilizing Agrobacterium-mediated leaf disc method. We have constructed total eight different constructs for the lignin related gene family CCoAMT, out of which three constructs have been selected from Ntab0184090, two constructs from Ntab0392460 while one construct from each Ntab0540120, Ntab0857410 and Ntab0135940 gene. To study the Cas9 system in pectin related genes, total five constructs have been utilized under Cas9 system and multiple target sites were selected by identifying PAM sequences. Out of which three constructs were targeted from NtabGAE1and NtabGAE6 homologous while two were targeted from NtabGAUT4 homologous. Where as, UDP-D-glucuronate 4-epimerase gene family is a Golgi localized, might have a role in the interconvertion of UDP-D-GlcA and UDP-D-GalA in pectin synthesis. We have succeeded in the mutation of pectin related NtabGAUT4 and lignin related NtabCCoAMT genes with 6.2% and 9.4% mutation frequency.

摘要

CRISPR/Cas9 系统已成功应用于动植物,是第二代基因组编辑工具。我们能够优化 Cas9 系统,分别编辑 HD 和 K326 烟草品种中的 Ntab06050 和 Ntab0857410 基因。基因 Ntab06050 与木质素合成有关,而基因 Ntab0857410 则属于果胶合成,我们利用农杆菌介导的叶盘法进行基因编辑。我们构建了总共 8 种不同的木质素相关基因家族 CCoAMT 的构建体,其中 3 种来自 Ntab0184090,2 种来自 Ntab0392460,1 种来自 Ntab0540120、Ntab0857410 和 Ntab0135940。为了研究 Cas9 系统在果胶相关基因中的作用,我们总共利用了 5 种构建体,通过识别 PAM 序列选择了多个靶位点。其中 3 种来自 NtabGAE1 和 NtabGAE6 同源基因,2 种来自 NtabGAUT4 同源基因。而 UDP-D-葡萄糖醛酸 4-差向异构酶基因家族是一种高尔基体定位的酶,可能在果胶合成中 UDP-D-GlcA 和 UDP-D-GalA 的相互转化中发挥作用。我们成功地使果胶相关 NtabGAUT4 和木质素相关 NtabCCoAMT 基因发生了突变,突变频率分别为 6.2%和 9.4%。

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