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1.550004 贵阳,贵州医科大学细胞工程生物医药技术国家地方联合工程实验室,基础医学院免疫学教研室,贵州省再生医学重点实验室
2.550004 贵阳,中国医学科学院成体干细胞转化研究重点实验室
[舒莉萍,E-mail:gyslp456@gmc.edu.cn SHU Liping, E-mail: gyslp456@gmc.edu.cn
收稿:2020-10-27,
修回:2021-01-04,
纸质出版:2021-04-30
移动端阅览
彭涛, 周唯君, 刘含, 等. CRISPR/Cas9技术敲除斑马鱼
Tao PENG, Weijun ZHOU, Han LIU, et al. Effects of
彭涛, 周唯君, 刘含, 等. CRISPR/Cas9技术敲除斑马鱼
Tao PENG, Weijun ZHOU, Han LIU, et al. Effects of
目的
2
利用CRISPR/Cas9技术敲除斑马鱼
rpl15
基因,探讨
rpl15
基因对斑马鱼红系造血发育的影响。
方法
2
针对斑马鱼
rpl15
基因设计并制备gRNA(guide RNA),将gRNA与Cas9蛋白的混合物显微注射到单细胞期斑马鱼受精卵中,提取72 h胚胎基因组DNA,PCR扩增出目的片段,T7E1限制性酶切法检测基因打靶情况,随后进行测序分析确定编辑效果。通过O-dianisidine染色分析血红蛋白合成情况,中性粒细胞染色分析中性粒细胞生成情况,利用Real-time PCR检测
p53
、
mdm2
、
hsp70
和造血相关转录因子基因的表达变化。
结果
2
成功制备了
rpl15
gRNA
并筛选得到
rpl15
突变体。
rpl15
基因敲除的幼鱼出现体长缩短、尾部弯曲、头部和眼睛较小及心包水肿的表型;造血相关谱系染色结果显示
rpl15
突变体血红蛋白合成明显减少,但中性粒细胞生成未受影响;
rpl15
突变体
p 53
和
mdm2
的mRNA表达均显著升高(
P
<
0.01,
P
<
0.05
),
α-globin
、
gata1
和
hsp70
的mRNA表达均显著下调(
P
<
0.01,
P
<
0.05,
P
<
0.05),除红系外的造血相关转录因子的mRNA表达与对照组相比均无明显差异。
结论
2
利用CRISPR/Cas9技术成功编辑了斑马鱼
rpl15
基因,突变体产生了类似先天性纯红细胞再生障碍性贫血疾病的表型。同时表明
p53
与
hsp70
可能参与调控突变体表型的形成。
Objective
2
To determine the effect of knocking out zebrafish
rpl15
gene by CRISPR/Cas9 editing technique on zebrafish erythroid hematopoietic d
evelopment.
Methods
2
Guide RNA was designed and prepared for
rpl15
gene of zebrafish and the mixture of gRNA and Cas9 protein was microinjected into zebrafish zygote at single cell stage. Genomic DNA was extracted after 72 h and the target fragment was amplified by PCR. Editing effect was evaluated by T7E1 restriction enzyme digestion of the PCR products followed by DNA sequencing. Hemoglobin synthesis was analyzed by O-dianisidine staining
neutrophil production was analyzed by neutrophil staining
and the expression of
p53
mdm2
hsp70
and hematopoiesis related transcription factor genes was detected by real-time PCR.
Results
2
The
rpl15
gRNA was successfully prepared and the
rpl15
mutants were selected. The results showed that zebrafish
rpl15
gene knockout juveniles showed a phenotype of shortened body length
curved tail
smaller head and eyes
and pericardial edema. Hematopoietic lineage staining showed that hemoglobin synthesis in
rpl15
mutant was significantly decreased
but neutrophil production was not affected. The mRNA expression levels of
rpl15
mutant
p53
and
mdm2
were significantly increased (
P
<
0.01
P
<
0.05)
while those of
α-globin
gata 1
and
hsp70
were obviously down-regulated (
P
<
0.01
P
<
0.05
P
<
0.05). There were no significant differences between the
rpl15
mutant and the control group in the mRNA expression levels of hematopoiesis-related transcription factors except erythroid-related ones.
Conclusion
2
The
rpl15
gene of zebrafish is successfully edited by CRISPR/Cas9 technique
and the mutant produces a phenotype similar to Di
amoncl-Blackfan anemia disease. At the same time
it is suggested that
p53
and
hsp70
may be involved in regulating the formation of mutant phenotype.
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