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基因工程多顺反子 Pmel 等位基因在黑素细胞谱系中产生高度特异性的 CreERT2 介导的重组。

Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineage.

机构信息

Division of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster, UK.

MRC Human Genetics Unit, Institute of Genetics and Cancer, Western General Hospital, University of Edinburgh, Edinburgh, UK.

出版信息

Pigment Cell Melanoma Res. 2023 Jan;36(1):71-77. doi: 10.1111/pcmr.13076. Epub 2022 Dec 19.

Abstract

Genetic approaches that allow lineage tracing are essential to our future understanding of melanocytes and melanoma. To date, the approaches used to label melanocytes in mice have relied on random integration of transgenes driven by the promoters of the Tyrosinase and Dopachrome tautomerase genes, knock-in to the Dopachrome tautomerase locus or knock-in to the Mlana locus in a bacterial artificial chromosome. These strategies result in expression in other tissues such as telencephalon and other cell types such as nerves. Here we used homologous recombination in mouse embryonic stem cells to generate a targeted multicistronic allele of the Pmel locus that drives melanocyte-specific expression of CreERT2, nuclear localised H2B-Cerulean and membrane localised marcks-mKate2 allowing live imaging of melanocytes and activation of other conditional alleles. We combined this allele with R26R-EYFP mice allowing induction of EYFP expression on administration of tamoxifen or its metabolite 4-OHT. The fluorescent proteins H2B-Cerulean and marcks-mKate2 label the cell nucleus and plasma membrane respectively allowing live imaging and FACS isolation of melanoblasts and melanocytes as well as serving to provide an internal control allowing estimation of recombination efficiency after administration of tamoxifen. We demonstrate the utility of the transgene in embryonic and adult tissues.

摘要

遗传方法,允许谱系追踪,是我们未来理解黑素细胞和黑色素瘤的关键。迄今为止,用于标记小鼠黑素细胞的方法依赖于由酪氨酸酶和多巴色素互变异构酶基因启动子驱动的转基因的随机整合,敲入多巴色素互变异构酶基因座或敲入细菌人工染色体中的 Mlana 基因座。这些策略导致在其他组织如大脑皮层和其他细胞类型如神经中表达。在这里,我们使用同源重组在小鼠胚胎干细胞中生成 Pmel 基因座的靶向多顺反子等位基因,该等位基因驱动 CreERT2、核定位 H2B-Cerulean 和膜定位 marcks-mKate2 在黑素细胞中的特异性表达,允许黑素细胞的活体成像和其他条件等位基因的激活。我们将这个等位基因与 R26R-EYFP 小鼠结合,允许在给予他莫昔芬或其代谢物 4-OHT 时诱导 EYFP 表达。荧光蛋白 H2B-Cerulean 和 marcks-mKate2 分别标记细胞核和质膜,允许活体成像和 FACS 分离黑素母细胞和黑素细胞,并作为内部对照,允许在给予他莫昔芬后估计重组效率。我们证明了该转基因在胚胎和成年组织中的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e45/10107733/d9e72b8bf468/PCMR-36-71-g001.jpg

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