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利用慢病毒载体高效地对培养的原始生殖细胞进行基因组修饰,以产生转基因鸣禽。

Highly Efficient Genome Modification of Cultured Primordial Germ Cells with Lentiviral Vectors to Generate Transgenic Songbirds.

机构信息

Max Planck Institute for Ornithology, Eberhard Gwinner Strasse, 82319 Seewiesen, Germany.

Max Planck Institute for Ornithology, Eberhard Gwinner Strasse, 82319 Seewiesen, Germany.

出版信息

Stem Cell Reports. 2021 Apr 13;16(4):784-796. doi: 10.1016/j.stemcr.2021.02.015. Epub 2021 Mar 18.

Abstract

The ability to genetically manipulate organisms has led to significant insights into functional genomics in many species. In birds, manipulation of the genome is hindered by the inaccessibility of the one-cell embryo. During embryonic development, avian primordial germ cells (PGCs) migrate through the bloodstream and reach the gonadal anlage, where they develop into mature germ cells. Here, we explored the use of PGCs to produce transgenic offspring in the zebra finch, which is a major animal model for sexual brain differentiation, vocal learning, and vocal communication. Zebra finch PGCs (zfPGCs) obtained from embryonic blood significantly proliferated when cultured in an optimized culture medium and conserved the expression of germ and stem cell markers. Transduction of cultured zfPGCs with lentiviral vectors was highly efficient, leading to strong expression of the enhanced green fluorescent protein. Transduced zfPGCs were injected into the host embryo and transgenic songbirds were successfully generated.

摘要

基因操作技术使人们能够深入了解许多物种的功能基因组学。然而,鸟类基因组的操作受到一细胞胚胎难以接近的限制。在胚胎发育过程中,禽类原始生殖细胞(PGCs)通过血液迁移并到达生殖嵴原基,在那里它们发育成成熟的生殖细胞。在这里,我们探索了利用 PGCs 在斑马雀中产生转基因后代的方法,斑马雀是性脑分化、发声学习和发声交流的主要动物模型。从胚胎血液中获得的斑马雀 PGC(zfPGCs)在优化的培养基中大量增殖,并保持生殖细胞和干细胞标记物的表达。慢病毒载体对培养的 zfPGCs 的转导效率非常高,导致增强型绿色荧光蛋白的强烈表达。转导的 zfPGCs 被注入宿主胚胎中,并成功生成了转基因鸣禽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3df5/8072032/8e4fed2d05ab/fx1.jpg

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