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病毒和腺病毒受体的同种型特异性编辑。

Isoform specific editing of the coxsackievirus and adenovirus receptor.

机构信息

Biomedical Sciences PhD Program, Wright State University, Dayton, OH, 45435, USA; Boonshoft School of Medicine, Wright State University, Dayton, OH, 45435, USA.

Department of Biological Sciences, Wright State University, Dayton, OH, 45435, USA.

出版信息

Virology. 2019 Oct;536:20-26. doi: 10.1016/j.virol.2019.07.018. Epub 2019 Jul 27.

Abstract

The Coxsackievirus and adenovirus receptor (CAR) is both a viral receptor and cell adhesion protein. CAR has two transmembrane isoforms that localize distinctly in polarized epithelial cells. Whereas the seven exon-encoded isoform (CAR) exhibits basolateral localization, the eight exon-encoded isoform (CAR) can localize to the apical epithelial surface where it can mediate luminal adenovirus infection. To further understand the distinct biological functions of these two isoforms, CRISPR/Cas9 genomic editing was used to specifically delete the eighth exon of the CXADR gene in a Madine Darby Canine Kidney (MDCK) cell line with a stably integrated lentiviral doxycycline-inducible CAR cDNA. The gene-edited clone demonstrated a significant reduction in adenovirus susceptibility when both partially and fully polarized, and doxycycline-induction of CAR restored sensitivity to adenovirus. These data reinforce the importance of CAR in apical adenovirus infection and provide a new model cell line to probe isoform specific biological functions of CAR.

摘要

柯萨奇病毒和腺病毒受体 (CAR) 既是一种病毒受体,也是一种细胞黏附蛋白。CAR 有两种跨膜异构体,它们在极化的上皮细胞中定位明显不同。七个外显子编码的异构体 (CAR) 表现为基底外侧定位,而八个外显子编码的异构体 (CAR) 可以定位到上皮表面的顶端,在那里它可以介导管腔腺病毒感染。为了进一步了解这两种异构体的独特生物学功能,使用 CRISPR/Cas9 基因组编辑技术特异性删除了带有稳定整合的慢病毒强力霉素诱导型 CAR cDNA 的 Madine Darby Canine Kidney (MDCK) 细胞系中 CXADR 基因的第八个外显子。当部分和完全极化时,基因编辑克隆显示出对腺病毒敏感性显著降低,并且 CAR 的强力霉素诱导恢复了对腺病毒的敏感性。这些数据强调了 CAR 在顶端腺病毒感染中的重要性,并提供了一种新的模型细胞系来探索 CAR 的异构体特异性生物学功能。

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