Y染色体造血缺失小鼠模型的建立。

Soichi Sano, Kenneth Walsh
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摘要

该方案描述了嵌合小鼠的产生,其中Y染色体从一定比例的血细胞中删除。该模型概括了Y染色体造血马赛克缺失(mLOY)的现象,这种现象在老年男性血液中经常观察到。为了构建造血Y染色体缺失的小鼠,从ROSA26-Cas9敲入小鼠的骨髓中分离出谱系阴性细胞。这些细胞用慢病毒载体进行转导,慢病毒载体编码引导RNA (gRNA),靶向Y染色体着丝粒的多次重复,有效地去除Y染色体。然后将这些细胞移植到经过致死照射的野生型C57BL6小鼠体内。对照grna被设计为不针对特定区域或肌动蛋白基因的第四个内含子。通过测量表达病毒编码的报告基因tRFP的血细胞的比例来跟踪转导细胞。该模型代表了Y染色体造血马赛克缺失的临床相关模型,可用于研究mLOY对各种年龄相关疾病的影响。图形的概述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Development of a Mouse Model of Hematopoietic Loss of Y Chromosome.

This protocol describes the generation of chimeric mice in which the Y chromosome is deleted from a proportion of blood cells. This model recapitulates the phenomenon of hematopoietic mosaic loss of Y chromosome (mLOY), which is frequently observed in the blood of aged men. To construct mice with hematopoietic Y chromosome loss, lineage-negative cells are isolated from the bone marrow of ROSA26-Cas9 knock-in mice. These cells are transduced with a lentivirus vector encoding a guide RNA (gRNA) that targets multiple repeats of the Y chromosome centromere, effectively removing the Y chromosome. These cells are then transplanted into lethally irradiated wildtype C57BL6 mice. Control gRNAs are designed to target either no specific region or the fourth intron of Actin gene. Transduced cells are tracked by measuring the fraction of blood cells expressing the virally encoded reporter gene tRFP. This model represents a clinically relevant model of hematopoietic mosaic loss of Y chromosome, which can be used to study the impact of mLOY on various age-related diseases. Graphical overview.

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