CRISPR-based genome editing in primary human pancreatic islet cells.

CRISPR-based genome editing in primary human pancreatic islet cells.
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DOI:
10.1038/s41467-021-22651-w
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发表时间:
2021-04-23
影响因子:
16.6
通讯作者:
Kim SK
Kim SK
中科院分区:
综合性期刊1区
文献类型:
--
作者:
Bevacqua RJ;Dai X;Lam JY;Gu X;Friedlander MSH;Tellez K;Miguel-Escalada I;Bonàs-Guarch S;Atla G;Zhao W;Kim SH;Dominguez AA;Qi LS;Ferrer J;MacDonald PE;Kim SK

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在原代人类胰岛中进行基因打靶研究可以促进我们对糖尿病发病机制的理解。在这里,我们展示了使用成簇的规则间隔短回文重复序列(CRISPR)和CRISPR相关蛋白9(Cas9)在原始人类胰岛中成功地进行基因组编辑。基于CRISPR的靶向有效突变的蛋白质编码外显子,导致胰岛β细胞调节因子的急性丢失,如转录因子PDX1和KATP通道亚单位KIR6.2,伴随着β细胞调节和功能的受损。CRISPR靶向携带2型糖尿病(T2D)风险变异体的非编码基因显示,ABCC8、SIX2和SIX3的表达发生变化,β细胞功能受损,从而将这些靶基因中的调控元件与T2D遗传易感性联系起来。这方面的进展为人类胰岛细胞的遗传学研究建立了一个范例,并揭示了将非编码变体与人类糖尿病风险联系起来的调节和遗传机制。对原发人类胰岛的编辑可以提供对糖尿病发病机制的洞察。在这里,作者使用CRISPR-CAS9来靶向与T2D易感性相关的调节元件。
Gene targeting studies in primary human islets could advance our understanding of mechanisms driving diabetes pathogenesis. Here, we demonstrate successful genome editing in primary human islets using clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated protein 9 (Cas9). CRISPR-based targeting efficiently mutated protein-coding exons, resulting in acute loss of islet β-cell regulators, like the transcription factor PDX1 and the KATP channel subunit KIR6.2, accompanied by impaired β-cell regulation and function. CRISPR targeting of non-coding DNA harboring type 2 diabetes (T2D) risk variants revealed changes in ABCC8, SIX2 and SIX3 expression, and impaired β-cell function, thereby linking regulatory elements in these target genes to T2D genetic susceptibility. Advances here establish a paradigm for genetic studies in human islet cells, and reveal regulatory and genetic mechanisms linking non-coding variants to human diabetes risk. The editing of primary human islets could provide insight into diabetes pathogenesis. Here the authors use CRISPR-Cas9 to target regulatory elements associated with T2D susceptibility.
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