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利用 CRISPR/Cas9 系统对水稻类基因家族进行靶向诱变揭示了 OsFWL4 作为调控水稻分蘖数和产量的一个因子。

Targeted Mutagenesis of the Rice -Like Gene Family Using the CRISPR/Cas9 System Reveals OsFWL4 as a Regulator of Tiller Number and Plant Yield in Rice.

机构信息

Jiangsu Collaborative Innovation Center of Regional Modern Agriculture & Environmental Protection/Jiangsu Key Laboratory for Eco-Agricultural Biotechnology around Hongze Lake, Huaiyin Normal University, Huai'an 223300, China.

Huaiyin Institute of Agricultural Sciences of Xuhuai Region in Jiangsu, Huai'an 223001, China.

出版信息

Int J Mol Sci. 2020 Jan 26;21(3):809. doi: 10.3390/ijms21030809.

DOI:10.3390/ijms21030809
PMID:31991936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7037146/
Abstract

The -like () genes encode cysteine-rich proteins with a placenta-specific 8 domain. They play roles in cell division and organ size control, response to rhizobium infection, and metal ion homeostasis in plants. Here, we target eight rice genes using the CRISPR/Cas9 system delivered by -mediated transformation. We successfully generate transgenic T lines for 15 of the 16 targets. The targeted mutations are detected in the T lines of all 15 targets and the average mutation rate is found to be 81.6%. Transfer DNA (T-DNA) truncation is a major reason for the failure of mutagenesis in T plants. T-DNA segregation analysis reveals that the T-DNA inserts in transgenic plants can be easily eliminated in the T generation. Of the 30 putative off-target sites examined, unintended mutations are detected in 13 sites. Phenotypic analysis reveals that tiller number and plant yield of gene mutants are significantly greater than those of the wild type. Flag leaves of gene mutants are wider than those of the wild type. The increase in leaf width of the mutants is caused by an increase in cell number. Additionally, grain length of gene mutants is higher than that of the wild type. Our results suggest that transgene-free rice plants with targeted mutations can be produced in the T generation using the -mediated CRISPR/Cas9 system and that the gene is a negative regulator of tiller number and plant yield.

摘要
  • 样()基因编码富含半胱氨酸的蛋白质,具有胎盘特异性 8 结构域。它们在细胞分裂和器官大小控制、对根瘤菌感染的反应以及植物体内金属离子稳态中发挥作用。在这里,我们使用农杆菌介导的 CRISPR/Cas9 系统靶向 8 个水稻基因。我们成功地为 16 个靶基因中的 15 个生成了转基因 T 系。在所有 15 个靶基因的 T 系中均检测到靶向突变,平均突变率为 81.6%。T-DNA 缺失是 T 系诱变失败的主要原因。T-DNA 分离分析表明,转基因植物中的 T-DNA 插入物可以在 T 代中轻易消除。在 30 个检查的潜在脱靶位点中,在 13 个位点检测到非预期突变。表型分析表明,基因突变体的分蘖数和植物产量明显大于野生型。基因突变体的旗叶比野生型宽。突变体叶片宽度的增加是由于细胞数量的增加所致。此外,基因突变体的粒长高于野生型。我们的结果表明,使用农杆菌介导的 CRISPR/Cas9 系统可以在 T 代中产生无转基因的靶向突变水稻植株,并且基因是分蘖数和植物产量的负调节剂。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/390d4838aca4/ijms-21-00809-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/4d44577475be/ijms-21-00809-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/a571079c1628/ijms-21-00809-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/fcab337588f3/ijms-21-00809-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/b7fc33b87042/ijms-21-00809-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/28e57cb6dbb0/ijms-21-00809-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/390d4838aca4/ijms-21-00809-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/4d44577475be/ijms-21-00809-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/a571079c1628/ijms-21-00809-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/fcab337588f3/ijms-21-00809-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/b7fc33b87042/ijms-21-00809-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/28e57cb6dbb0/ijms-21-00809-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e18/7037146/390d4838aca4/ijms-21-00809-g006.jpg

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