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条件性人类BRD4基因敲入转基因小鼠基因分型及蛋白质异构体检测

Conditional Human BRD4 Knock-In Transgenic Mouse Genotyping and Protein Isoform Detection.

作者信息

Lewis Michael Paul, Wu Shwu-Yuan, Chiang Cheng-Ming

机构信息

Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.

Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.

出版信息

Bio Protoc. 2022 Apr 5;12(7). doi: 10.21769/BioProtoc.4374.

Abstract

Bromodomain-containing protein 4 (BRD4) is an acetyl-lysine reader protein and transcriptional regulator implicated in chromatin dynamics and cancer development. Several BRD4 isoforms have been detected in humans with the long isoform (BRD4-L, aa 1-1,362) playing a tumor-suppressive role and a major short isoform (BRD4-S, aa 1-722) having oncogenic activity in breast cancer development. demonstration of the opposing functions of BRD4 protein isoforms requires development of mouse models, particularly transgenic mice conditionally expressing human BRD4-L or BRD4-S, which can be selectively induced in different mouse tissues in a spatiotemporal-specific manner. Here, we detail the procedures used to genotype transgenic mouse strains developed to define the effects of conditional human BRD4 isoform expression on polyomavirus middle T antigen (PyMT)-induced mouse mammary tumor growth, and the key steps for Western blot detection of BRD4 protein isoforms in those tumors and in cultured cells. With this protocol as a guide, interpretation of BRD4 isoform functions becomes more feasible and expandable to various biological settings. Adequate tracking of BRD4 isoform distributions and is key to understanding their biological roles, as well as avoiding misinterpretation of their functions due to improper use of experimental procedures that fail to detect their spatial and temporal distributions. Graphic abstract.

摘要

含溴结构域蛋白4(BRD4)是一种乙酰赖氨酸识别蛋白和转录调节因子,与染色质动态变化和癌症发展有关。在人类中已检测到几种BRD4异构体,其中长异构体(BRD4-L,氨基酸1-1362)发挥肿瘤抑制作用,而一种主要的短异构体(BRD4-S,氨基酸1-722)在乳腺癌发展中具有致癌活性。要证明BRD4蛋白异构体的相反功能,需要建立小鼠模型,特别是条件性表达人BRD4-L或BRD4-S的转基因小鼠,它们可以在不同的小鼠组织中以时空特异性方式被选择性诱导。在这里,我们详细介绍了用于对转基因小鼠品系进行基因分型的程序,这些品系用于确定条件性人BRD4异构体表达对多瘤病毒中T抗原(PyMT)诱导的小鼠乳腺肿瘤生长的影响,以及在这些肿瘤和培养细胞中通过蛋白质印迹法检测BRD4蛋白异构体的关键步骤。以该方案为指导,对BRD4异构体功能的解释变得更加可行,并且可以扩展到各种生物学环境。充分追踪BRD4异构体的分布对于理解它们的生物学作用以及避免因使用未能检测其空间和时间分布的实验程序不当而对其功能产生误解至关重要。图形摘要。

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