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CRISPR Cas9-and Cas12a-mediated gusA editing in transgenic blueberry | |
Han, Xiaoyan1; Yang, Yingzhen; Han, Xue; Ryner, John T.; Ahmed, Emadeldin A. H.; Qi, Yiping4; Zhong, Gan-Yuan; Song, Guo-Qing | |
2022 | |
发表期刊 | PLANT CELL TISSUE AND ORGAN CULTURE |
ISSN | 0167-6857 |
卷号 | 148期号:2页码:217-229 |
摘要 | Key Message A second round of regeneration enriched editing events and enhanced the production of edited blueberry shoots. The new protocol described facilitates high-precision breeding of blueberries using CRISPR Cas technologies. To develop an effective genome editing tool for blueberry breeding, CRISPR-Cas9 and CRISPR-Cas12a were evaluated for their editing efficiencies of a marker gene, beta-glucuronidase (gusA), which was previously introduced into two blueberry cultivars each a single-copy transgene. Four expression vectors were built, with CRISPR-Cas9 and CRISPR-Cas12a each driven by a 35S promoter or AtUbi promoter. Each vector contained two editing sites in the gusA. These four vectors were respectively transformed into the leaf explants of transgenic gusA blueberry and the resulting transgenic calli were induced under hygromycin selection. GUS staining showed that some small proportions of the hygromycin-resistant calli had non-GUS stained sectors, suggesting some possible occurrences of gusA editing. We sequenced GUS amplicons spanning the two editing sites in three blueberry tissues and found about 5.5% amplicons having editing features from the calli transformed with the 35S-Cas9 vector. Further, we conducted a second round of shoot regeneration from leaf explants derived from the initial Cas9- and Cas12a-containing calli (T-0) and analyzed amplicons of the target editing region. Of the newly induced shoots, 15.5% for the 35S-Cas9 and 5.3% for the AtUbi-Cas9 showed non-GUS staining, whereas all of the shoots containing the Cas12a vectors showed blue staining. Sanger sequencing confirmed the editing-induced mutations in two representative non-GUS staining lines. Clearly, the second round of regeneration had enriched editing events and enhanced the production of edited shoots. The results and protocol described will be helpful to facilitating high-precision breeding of blueberries using CRISPR Cas technologies. |
关键词 | Blueberry CRISPR-Cas9 CRISPR-Cas12a Gene editing GUS |
学科领域 | Biotechnology & Applied Microbiology ; Plant Sciences |
DOI | 10.1007/s11240-021-02177-1 |
收录类别 | SCI |
语种 | 英语 |
WOS关键词 | TARGETED MUTAGENESIS ; DNA ; PLANTS ; ARABIDOPSIS ; CANCER ; TISSUE ; WHEAT |
WOS研究方向 | Science Citation Index Expanded (SCI-EXPANDED) |
WOS记录号 | WOS:000709223900001 |
出版者 | SPRINGER |
文献子类 | Article |
出版地 | DORDRECHT |
EISSN | 1573-5044 |
资助机构 | USDA Agricultural Research Service and Michigan State University [58-8060-6-009] ; CAS Scholarship |
作者邮箱 | ganyuan.zhong@usda.gov ; songg@msu.edu |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://ir.ibcas.ac.cn/handle/2S10CLM1/28548 |
专题 | 植物园 |
作者单位 | 1.Michigan State Univ, Dept Hort, Plant Biotechnol Resource & Outreach Ctr, E Lansing, MI 48824 USA 2.Chinese Acad Sci, Beijing Bot Garden, Inst Bot, Beijing 100093, Peoples R China 3.USDA Agr Res Serv, Grape Genet Res Unit, Geneva, NY 14456 USA 4.Ahmed, Emadeldin A. H.] Agr Res Ctr, Breeding Res Dept Fruit Trees Ornamental & Woody, Inst Hort Res, Giza, Egypt 5.Univ Maryland, Dept Plant Sci & Landscape Architecture, College Pk, MD 20742 USA |
推荐引用方式 GB/T 7714 | Han, Xiaoyan,Yang, Yingzhen,Han, Xue,et al. CRISPR Cas9-and Cas12a-mediated gusA editing in transgenic blueberry[J]. PLANT CELL TISSUE AND ORGAN CULTURE,2022,148(2):217-229. |
APA | Han, Xiaoyan.,Yang, Yingzhen.,Han, Xue.,Ryner, John T..,Ahmed, Emadeldin A. H..,...&Song, Guo-Qing.(2022).CRISPR Cas9-and Cas12a-mediated gusA editing in transgenic blueberry.PLANT CELL TISSUE AND ORGAN CULTURE,148(2),217-229. |
MLA | Han, Xiaoyan,et al."CRISPR Cas9-and Cas12a-mediated gusA editing in transgenic blueberry".PLANT CELL TISSUE AND ORGAN CULTURE 148.2(2022):217-229. |
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Han-2022-CRISPR Cas9(2372KB) | 期刊论文 | 出版稿 | 开放获取 | CC BY-NC-SA | 浏览 请求全文 |
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