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C57BL/6 近交系遗传工程小鼠与其野生型对照品系的错配会导致混杂结果,这在对乙酰氨基酚和刀豆蛋白 A 肝损伤中 JNK2 的研究中就是如此。

Mispairing C57BL/6 substrains of genetically engineered mice and wild-type controls can lead to confounding results as it did in studies of JNK2 in acetaminophen and concanavalin A liver injury.

机构信息

Molecular and Cellular Toxicology Section, Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland 20892-1760, United States.

出版信息

Chem Res Toxicol. 2011 Jun 20;24(6):794-6. doi: 10.1021/tx200143x. Epub 2011 May 24.

DOI:10.1021/tx200143x
PMID:21557537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3157912/
Abstract

C57BL/6 mice are widely used in biomedical research for the background of genetically engineered mice (GEM) and wild-type controls with the belief that the genetic background of GEM and control mice differ significantly by only one or more altered genes. This principle, however, does have limitations due in part to the existence of multiple substrains of C57BL/6 mice that should not be used interchangeably as they can differ both genetically and phenotypically. We show here that these mispairings do occur frequently and can lead to inaccurate and conflicting findings.

摘要

C57BL/6 小鼠广泛应用于生物医学研究,其背景是基因工程小鼠(GEM)和野生型对照小鼠,人们认为 GEM 和对照小鼠的遗传背景仅因一个或多个改变的基因而有显著差异。然而,这一原则确实存在局限性,部分原因是 C57BL/6 小鼠存在多个亚系,这些亚系不应互换使用,因为它们在遗传和表型上都可能存在差异。我们在这里表明,这些错配经常发生,并可能导致不准确和相互矛盾的发现。

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Chem Res Toxicol. 2011 Jun 20;24(6):794-6. doi: 10.1021/tx200143x. Epub 2011 May 24.
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本文引用的文献

1
Genetic polymorphisms among C57BL/6 mouse inbred strains.C57BL/6 近交系小鼠的遗传多态性。
Transgenic Res. 2011 Jun;20(3):481-9. doi: 10.1007/s11248-010-9403-8. Epub 2010 May 27.
2
Diet-induced obesity in two C57BL/6 substrains with intact or mutant nicotinamide nucleotide transhydrogenase (Nnt) gene.两种具有完整或突变烟酰胺核苷酸转氢酶 (Nnt) 基因的 C57BL/6 亚系的饮食诱导肥胖。
Obesity (Silver Spring). 2010 Oct;18(10):1902-5. doi: 10.1038/oby.2009.477. Epub 2010 Jan 7.
3
Differences in aggressive behavior and DNA copy number variants between BALB/cJ and BALB/cByJ substrains.BALB/cJ 和 BALB/cByJ 亚系之间攻击行为和 DNA 拷贝数变异的差异。
Behav Genet. 2010 Mar;40(2):201-10. doi: 10.1007/s10519-009-9325-5. Epub 2009 Dec 23.
4
Effects of oats on plasma cholesterol and lipoproteins in C57BL/6 mice are substrain specific.燕麦对 C57BL/6 小鼠血浆胆固醇和脂蛋白的影响具有亚系特异性。
Br J Nutr. 2010 Feb;103(4):513-21. doi: 10.1017/S000711450999211X. Epub 2009 Oct 20.
5
Genetic differences among C57BL/6 substrains.C57BL/6亚系之间的遗传差异。
Exp Anim. 2009 Apr;58(2):141-9. doi: 10.1538/expanim.58.141.
6
Behavioral differences among C57BL/6 substrains: implications for transgenic and knockout studies.C57BL/6亚系之间的行为差异:对转基因和基因敲除研究的启示。
J Neurogenet. 2008;22(4):315-31. doi: 10.1080/01677060802357388.
7
Differential roles of JNK in ConA/GalN and ConA-induced liver injury in mice.JNK在刀豆蛋白A/氨基半乳糖和刀豆蛋白A诱导的小鼠肝损伤中的不同作用。
Am J Pathol. 2008 Oct;173(4):962-72. doi: 10.2353/ajpath.2008.080358. Epub 2008 Sep 4.
8
Deletion of apoptosis signal-regulating kinase 1 attenuates acetaminophen-induced liver injury by inhibiting c-Jun N-terminal kinase activation.凋亡信号调节激酶1的缺失通过抑制c-Jun氨基末端激酶激活减轻对乙酰氨基酚诱导的肝损伤。
Gastroenterology. 2008 Oct;135(4):1311-21. doi: 10.1053/j.gastro.2008.07.006. Epub 2008 Jul 9.
9
Protective role of c-Jun N-terminal kinase 2 in acetaminophen-induced liver injury.c-Jun氨基末端激酶2在对乙酰氨基酚诱导的肝损伤中的保护作用。
Biochem Biophys Res Commun. 2008 Sep 12;374(1):6-10. doi: 10.1016/j.bbrc.2008.06.065. Epub 2008 Jun 27.
10
Alcohol trait and transcriptional genomic analysis of C57BL/6 substrains.C57BL/6亚系的酒精特质与转录基因组分析。
Genes Brain Behav. 2008 Aug;7(6):677-89. doi: 10.1111/j.1601-183X.2008.00405.x. Epub 2008 Apr 7.