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通过腺病毒介导的体内基因编辑技术生成基因编辑鸡和鸭品系。

Generation of genome-edited chicken and duck lines by adenovirus-mediated in vivo genome editing.

机构信息

Department of Animal Sciences, The Ohio State University, Columbus, OH 43210.

Department of Animal Biotechnology, Kyungpook National University, Sangju 37224, South Korea.

出版信息

Proc Natl Acad Sci U S A. 2022 Nov 8;119(45):e2214344119. doi: 10.1073/pnas.2214344119. Epub 2022 Nov 2.

Abstract

Conventional avian genome editing is mediated by isolation, culture, and genome editing of primordial germ cells (PGCs); screening and propagating the genome-edited PGCs; and transplantation of the PGCs into recipient embryos. The PGC-mediated procedures, however, are technically difficult, and therefore, the conventional method has previously been utilized only in chickens. Here, we generated germline mosaic founder chicken and duck lines without the PGC-mediated procedures by injecting an adenovirus containing the CRISPR-Cas9 system into avian blastoderms. Genome-edited chicken and duck offspring produced from the founders carried different insertion or deletion mutations without mutations in the potential off-target sites. Our data demonstrate successful applications of the adenovirus-mediated method for production of genome-edited chicken and duck lines.

摘要

传统的禽类基因组编辑是通过分离、培养和基因组编辑原始生殖细胞(PGC)来介导的;筛选和繁殖经过基因组编辑的 PGC;然后将 PGC 移植到受体胚胎中。然而,PGC 介导的程序在技术上具有难度,因此,传统方法以前仅在鸡中使用。在这里,我们通过将含有 CRISPR-Cas9 系统的腺病毒注射到禽类囊胚中,生成了无需 PGC 介导程序的种系嵌合鸡和鸭系的创始者。由创始者产生的基因组编辑鸡和鸭后代携带不同的插入或缺失突变,而潜在的脱靶位点没有突变。我们的数据证明了腺病毒介导的方法在生产基因组编辑鸡和鸭系中的成功应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d55b/9659352/7fcea2972e00/pnas.2214344119fig01.jpg

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