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用于颅面研究的小鼠资源。

Mouse resources for craniofacial research.

作者信息

Murray Stephen A

机构信息

The Jackson Laboratory, Bar Harbor, Maine, USA.

出版信息

Genesis. 2011 Apr;49(4):190-9. doi: 10.1002/dvg.20722. Epub 2011 Apr 1.

Abstract

The mouse, as a genetically defined and easily manipulated model organism, has played a critical role in unraveling the mechanisms of craniofacial development and dysmorphology. While numerous gene knockout strains that display craniofacial abnormalities and essential recombinase tool strains with craniofacial-specific expression have been generated, many are absent from public repositories. Large-scale, international resource-generating initiatives promise to address this concern, providing a comprehensive set of targeted mutations and a suite of new Cre driver strains. In addition, panels of genetically defined strains provide tools to dissect the multigenic, complex nature of craniofacial development, adding to the foundation of information gained from single gene studies. Continued progress will require awareness and access to these essential mouse resources. In this review, current mouse resources, large-scale efforts, and potential future directions will be outlined and discussed.

摘要

小鼠作为一种基因定义明确且易于操作的模式生物,在揭示颅面发育和畸形机制方面发挥了关键作用。虽然已经产生了许多表现出颅面异常的基因敲除品系以及具有颅面特异性表达的重要重组酶工具品系,但许多品系并未存于公共资源库中。大规模的国际资源生成计划有望解决这一问题,提供一套全面的靶向突变和一系列新的Cre驱动品系。此外,基因定义品系组提供了剖析颅面发育多基因、复杂本质的工具,为从单基因研究中获得的信息基础增添了内容。持续的进展将需要了解并获取这些重要的小鼠资源。在本综述中,将概述并讨论当前的小鼠资源、大规模研究工作以及潜在的未来方向。

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本文引用的文献

1
Cre recombinase resources for conditional mouse mutagenesis.
Methods. 2011 Apr;53(4):411-6. doi: 10.1016/j.ymeth.2010.12.027. Epub 2010 Dec 31.
2
The mouse Gene Expression Database (GXD): 2011 update.
Nucleic Acids Res. 2011 Jan;39(Database issue):D835-41. doi: 10.1093/nar/gkq1132. Epub 2010 Nov 9.
3
The Mouse Genome Database (MGD): premier model organism resource for mammalian genomics and genetics.
Nucleic Acids Res. 2011 Jan;39(Database issue):D842-8. doi: 10.1093/nar/gkq1008. Epub 2010 Nov 3.
4
The IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse Consortium.
Nucleic Acids Res. 2011 Jan;39(Database issue):D849-55. doi: 10.1093/nar/gkq879. Epub 2010 Oct 6.
6
Disheveled hair and ear (Dhe), a spontaneous mouse Lmna mutation modeling human laminopathies.
PLoS One. 2010 Apr 1;5(4):e9959. doi: 10.1371/journal.pone.0009959.
9
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain.
Nat Neurosci. 2010 Jan;13(1):133-40. doi: 10.1038/nn.2467. Epub 2009 Dec 20.
10
Prdm16 is required for normal palatogenesis in mice.
Hum Mol Genet. 2010 Mar 1;19(5):774-89. doi: 10.1093/hmg/ddp543. Epub 2009 Dec 11.

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