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体重减轻是小鼠基因敲除后的常见效应。

Reduced body weight is a common effect of gene knockout in mice.

作者信息

Reed Danielle R, Lawler Maureen P, Tordoff Michael G

机构信息

Monell Chemical Senses Center, Philadelphia, USA.

出版信息

BMC Genet. 2008 Jan 8;9:4. doi: 10.1186/1471-2156-9-4.

DOI:10.1186/1471-2156-9-4
PMID:18182103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2263071/
Abstract

BACKGROUND

During a search for obesity candidate genes in a small region of the mouse genome, we noticed that many genes when knocked out influence body weight. To determine whether this was a general feature of gene knockout or a chance occurrence, we surveyed the Jackson Laboratory Mouse Genome Database for knockout mouse strains and their phenotypes. Body weights were not available for all strains so we also obtained body weight information by contacting a random sample of investigators responsible for a knockout strain.

RESULTS

We classified each knockout mouse strain as (1) lighter and smaller, (2) larger and heavier, or (3) the same weight, relative to control mice. We excluded knockout strains that died early in life, even though this type of lethality is often associated with a small embryo or reduced body size. Based on a dataset of 1,977 knockout strains, we found that that 31% of viable knockout mouse strains weighed less and an additional 3% weighed more than did controls.

CONCLUSION

Body weight is potentially a latent variable in about a third of experiments that use knockout mice and should be considered in interpreting experimental outcomes, e.g., in studies of hypertension, drug and hormone metabolism, organ development, cell proliferation and apoptosis, digestion, heart rate, or atherosclerosis. If we assume that the knockout genes we surveyed are representative then upward of 6,000 genes are predicted to influence the size of a mouse. Body weight is highly heritable, and numerous quantitative trait loci have been mapped in mice, but "multigenic" is an insufficient term for the thousands of loci that could contribute to this complex trait.

摘要

背景

在对小鼠基因组的一个小区域进行肥胖候选基因搜索时,我们注意到许多基因被敲除后会影响体重。为了确定这是基因敲除的普遍特征还是偶然现象,我们在杰克逊实验室小鼠基因组数据库中调查了基因敲除小鼠品系及其表型。并非所有品系都有体重数据,因此我们还通过联系负责某个基因敲除品系的研究人员随机样本获取了体重信息。

结果

我们将每个基因敲除小鼠品系相对于对照小鼠分类为:(1) 更轻更小;(2) 更大更重;或 (3) 体重相同。我们排除了生命早期死亡的基因敲除品系,尽管这种致死性通常与小胚胎或体型减小有关。基于1977个基因敲除品系的数据集,我们发现31% 的存活基因敲除小鼠品系体重比对照轻,另外3% 比对照重。

结论

在大约三分之一使用基因敲除小鼠的实验中,体重可能是一个潜在变量,在解释实验结果时应予以考虑,例如在高血压、药物和激素代谢、器官发育、细胞增殖与凋亡、消化、心率或动脉粥样硬化研究中。如果我们假设我们调查的基因敲除基因具有代表性,那么预计有超过6000个基因会影响小鼠的体型。体重具有高度遗传性,并且在小鼠中已经定位了许多数量性状基因座,但“多基因”对于可能导致这种复杂性状的数千个基因座来说是一个不够充分的术语。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccbf/2263071/996cd205b32e/1471-2156-9-4-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccbf/2263071/996cd205b32e/1471-2156-9-4-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccbf/2263071/996cd205b32e/1471-2156-9-4-1.jpg

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本文引用的文献

1
Interpretation of knockout experiments: the congenic footprint.基因敲除实验的解读:同源基因足迹
Genes Brain Behav. 2007 Apr;6(3):299-303. doi: 10.1111/j.1601-183X.2007.00304.x. Epub 2007 Feb 26.
2
Inheritance in the House Mouse, the Linkage Relations of Short-Ear, Hairless, and Naked.家鼠的遗传,短耳、无毛和裸鼠的连锁关系。
Genetics. 1931 Jan;16(1):42-74. doi: 10.1093/genetics/16.1.42.
3
A mouse for all reasons.适用于各种情况的小鼠。
饲养环境持续从分子到行为水平调节小鼠表型。
PLoS Biol. 2022 Oct 21;20(10):e3001837. doi: 10.1371/journal.pbio.3001837. eCollection 2022 Oct.
4
The Combined Inactivation of Intestinal and Hepatic ZIP14 Exacerbates Manganese Overload in Mice.肠肝 ZIP14 联合失活加剧小鼠锰过载。
Int J Mol Sci. 2022 Jun 10;23(12):6495. doi: 10.3390/ijms23126495.
5
Decomposing phenotypic skew and its effects on the predicted response to strong selection.分解表型偏度及其对强选择预测响应的影响。
Nat Ecol Evol. 2022 Jun;6(6):774-785. doi: 10.1038/s41559-022-01694-2. Epub 2022 Apr 14.
6
What is the optimum design for my animal experiment?我的动物实验的最佳设计是什么?
BMJ Open Sci. 2021 Mar 15;5(1):e100126. doi: 10.1136/bmjos-2020-100126. eCollection 2021.
7
Gene expression atlas of energy balance brain regions.能量平衡脑区的基因表达图谱。
JCI Insight. 2021 Aug 23;6(16):e149137. doi: 10.1172/jci.insight.149137.
8
Non-additive association analysis using proxy phenotypes identifies novel cattle syndromes.基于代理表型的非加性关联分析鉴定新的牛综合征。
Nat Genet. 2021 Jul;53(7):949-954. doi: 10.1038/s41588-021-00872-5. Epub 2021 May 27.
9
AAV9 transduction mediated by systemic delivery of vector via retro-orbital injection in newborn, neonatal and juvenile mice.经眶后注射系统递送载体的 AAV9 转导在新生、新生儿和幼年小鼠中的作用。
Exp Anim. 2021 Nov 10;70(4):450-458. doi: 10.1538/expanim.20-0186. Epub 2021 May 25.
10
Genetic analysis of body weight in wild populations of medaka fish from different latitudes.对来自不同纬度的野生青鳉鱼群体体重的遗传分析。
PLoS One. 2020 Jun 16;15(6):e0234803. doi: 10.1371/journal.pone.0234803. eCollection 2020.
Cell. 2007 Jan 12;128(1):9-13. doi: 10.1016/j.cell.2006.12.018.
4
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Mamm Genome. 2006 Nov;17(11):1065-77. doi: 10.1007/s00335-006-0054-2. Epub 2006 Nov 10.
5
Understanding mammalian genetic systems: the challenge of phenotyping in the mouse.理解哺乳动物遗传系统:小鼠表型分析的挑战。
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6
Ensembl 2006.Ensembl 2006。
Nucleic Acids Res. 2006 Jan 1;34(Database issue):D556-61. doi: 10.1093/nar/gkj133.
7
The Mouse Genome Database (MGD): from genes to mice--a community resource for mouse biology.小鼠基因组数据库(MGD):从基因到小鼠——小鼠生物学的社区资源。
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D471-5. doi: 10.1093/nar/gki113.
8
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Diabetes. 2004 Dec;53(12):3274-85. doi: 10.2337/diabetes.53.12.3274.
9
The knockout mouse project.基因敲除小鼠项目。
Nat Genet. 2004 Sep;36(9):921-4. doi: 10.1038/ng0904-921.
10
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Genetics. 2004 Jun;167(2):761-81. doi: 10.1534/genetics.104.026427.