pgRNA-Cas9系统敲除MKL1可抑制细胞迁移和增殖

Hong-Bo Liu, Ze Yin, Peng Zheng, Yao Xu, Zhen-yu Wang, Xi Li, Tong-Cun Zhang
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引用次数: 0

摘要

摘要作为一种转录因子,巨核细胞白血病1(MKL1)与血清反应因子(SRF)结合,调节靶基因的表达。因此,它参与了多种细胞过程,如癌症细胞的迁移、增殖和分化。然而,关于使用CRISPR–Cas9系统在人类基因组中敲除MKL1表达的报道很少。因此,构建了配对引导RNA(pgRNA)文库,并使用pgRNA–Cas9系统删除HeLa细胞中MKL1的表达。结果表明,通过蛋白质印迹法,MKL1的表达降低了95%。创伤愈合实验和MTT实验表明,MKL1的缺失抑制了细胞的迁移和增殖。此外,肿瘤抑制因子p21、p53、pRB和DLC1的蛋白表达水平在MKL1缺失后发生变化。这些数据表明,肿瘤抑制因子p21、p53、pRB和DLC1可能在MKL1缺失细胞的生长和迁移中发挥重要作用。
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Using pgRNA–Cas9 system to knockout MKL1 inhibited cell migration and proliferation
Abstract As a transcription factor, megakaryoblastic leukemia 1 (MKL1) binds with serum response factor (SRF) to regulate targeted genes expression. Therefore, it involved in various cellular processes, such as cancer cells migration, proliferation and differentiation. However, the report about knockout MKL1 expression using CRISPR–Cas9 system in human genome is rare. Therefore, paired-guide RNA (pgRNA) library was constructed, and pgRNA–Cas9 system was used to delete MKL1 expression in HeLa cells. The result showed that the expression of MKL1 was decreased 95% by Western blotting. And wound healing assay and MTT assay indicated that depletion MKL1 inhibited cell migration and proliferation. Additionally, the protein expression levels of tumor suppressor factors p21, p53, pRB and DLC1 were changed after depletion MKL1. These data suggested that tumor suppressor factors p21, p53, pRB and DLC1 maybe played an important role in the cell growth and migration of MKL1-depletion cells.
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Cogent Biology
Cogent Biology MULTIDISCIPLINARY SCIENCES-
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