β-Thalassemia is a global health issue, caused by mutations in the HBB gene. Among these mutations, HBB -28 （A〉G） mutations is one of the three most common mutations in China and Southeast Asia patients with β-th...β-Thalassemia is a global health issue, caused by mutations in the HBB gene. Among these mutations, HBB -28 （A〉G） mutations is one of the three most common mutations in China and Southeast Asia patients with β-thalassemia. Correcting this mutation in human embryos may prevent the disease being passed onto future generations and cure anemia. Here we report the first study using base editor （BE） system to correct disease mutant in human embryos. Firstly, we produced a 293T cell line with an exogenous HBB -28 （A〉G） mutant fragment for gRNAs and targeting efficiency evaluation. Then we collected primary skin fibroblast cells from a β-thalassemia patient with HBB -28 （A〉G） homozygous mutation. Data showed that base editor could precisely correct HBB -28 （A〉G） mutation in the patient＇s primary cells. To model homozygous mutation disease embryos, we consb＇ucted nuclear transfer embryos by fusing the lymphocyte or skin fibroblast cells with enucleated in vitro matured （IVM） oocytes.Notably, the gene correction efficiency was over 23.0% in these embryos by base editor. Although these embryos were still mosaic, the percentage of repaired blastomeres was over 20.0%. In addition, we found that base editor variants, with narrowed deamination window, could promote G-to-A conversion at HBB -28 site precisely in human embryos. Collectively, this study demonstrated the feasibility of curing genetic disease in human somatic cells and embryos by base editor system.展开更多
以亚洲百合品种Pollyanna和东方百合品种Sorbonne为试材,在比较异硫氰酸胍法、SDS/酚法与CTAB-L i Cl法提取总RNA效果的基础上,针对百合组织中富含多糖的特点,在Sorbonne提取RNA中加入特殊除多糖步骤,改进了CTAB- L i Cl法.结果表明,改...以亚洲百合品种Pollyanna和东方百合品种Sorbonne为试材,在比较异硫氰酸胍法、SDS/酚法与CTAB-L i Cl法提取总RNA效果的基础上,针对百合组织中富含多糖的特点,在Sorbonne提取RNA中加入特殊除多糖步骤,改进了CTAB- L i Cl法.结果表明,改进CTAB- L i Cl法能有效去除多糖,提取到的RNA2 8S r RNA亮度约为18S r RNA的2倍,A2 6 0 / 2 80介于1.8～2 .0之间,A2 6 0 / 2 30为2 .0 ,Pollyanna RNA产率为36 .3μL·g- 1 ,Sor-bonne RNA产率为10 .2 μL·g- 1 ,经RT- PCR获得了特异性条带,说明用改进CTAB- L i Cl法从百合花瓣中提取到的RNA质量好、产率高、完整性强,完全适合于进一步的分子生物学研究.展开更多
基金We are grateful to Dr. Qi Zhou for helpful suggestions. This work was supported by National Key R＆D Program of China （2017YFC1001901 and 2017YFC1001600）, the Science and Technology Planning Project of Guangdong Province （2015B020228002）, the Guangzhou Science and Technology Project （201707010085） and the National Natural Science Foundation of China （Grant No. 81771579）.
文摘β-Thalassemia is a global health issue, caused by mutations in the HBB gene. Among these mutations, HBB -28 （A〉G） mutations is one of the three most common mutations in China and Southeast Asia patients with β-thalassemia. Correcting this mutation in human embryos may prevent the disease being passed onto future generations and cure anemia. Here we report the first study using base editor （BE） system to correct disease mutant in human embryos. Firstly, we produced a 293T cell line with an exogenous HBB -28 （A〉G） mutant fragment for gRNAs and targeting efficiency evaluation. Then we collected primary skin fibroblast cells from a β-thalassemia patient with HBB -28 （A〉G） homozygous mutation. Data showed that base editor could precisely correct HBB -28 （A〉G） mutation in the patient＇s primary cells. To model homozygous mutation disease embryos, we consb＇ucted nuclear transfer embryos by fusing the lymphocyte or skin fibroblast cells with enucleated in vitro matured （IVM） oocytes.Notably, the gene correction efficiency was over 23.0% in these embryos by base editor. Although these embryos were still mosaic, the percentage of repaired blastomeres was over 20.0%. In addition, we found that base editor variants, with narrowed deamination window, could promote G-to-A conversion at HBB -28 site precisely in human embryos. Collectively, this study demonstrated the feasibility of curing genetic disease in human somatic cells and embryos by base editor system.
文摘以亚洲百合品种Pollyanna和东方百合品种Sorbonne为试材,在比较异硫氰酸胍法、SDS/酚法与CTAB-L i Cl法提取总RNA效果的基础上,针对百合组织中富含多糖的特点,在Sorbonne提取RNA中加入特殊除多糖步骤,改进了CTAB- L i Cl法.结果表明,改进CTAB- L i Cl法能有效去除多糖,提取到的RNA2 8S r RNA亮度约为18S r RNA的2倍,A2 6 0 / 2 80介于1.8～2 .0之间,A2 6 0 / 2 30为2 .0 ,Pollyanna RNA产率为36 .3μL·g- 1 ,Sor-bonne RNA产率为10 .2 μL·g- 1 ,经RT- PCR获得了特异性条带,说明用改进CTAB- L i Cl法从百合花瓣中提取到的RNA质量好、产率高、完整性强,完全适合于进一步的分子生物学研究.
