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全基因组条件性小鼠敲除资源

Genome Wide Conditional Mouse Knockout Resources.

作者信息

Kaloff C, Anastassiadis K, Ayadi A, Baldock R, Beig J, Birling M-C, Bradley A, Brown S, Bürger A, Bushell W, Chiani F, Collins F S, Doe B, Eppig J T, Finnel R H, Fletcher C, Flicek P, Fray M, Friedel R H, Gambadoro A, Gates H, Hansen J, Herault Y, Hicks G G, Hörlein A, Hrabé de Angelis M, Iyer V, de Jong P J, Koscielny G, Kühn R, Liu P, Lloyd K C, Lopez R G, Marschall S, Martínez S, McKerlie C, Meehan T, von Melchner H, Moore M, Murray S A, Nagy A, Nutter Lmj, Pavlovic G, Pombero A, Prosser H, Ramirez-Solis R, Ringwald M, Rosen B, Rosenthal N, Rossant J, Ruiz Noppinger P, Ryder E, Skarnes W C, Schick J, Schnütgen F, Schofield P, Seisenberger C, Selloum M, Smedley D, Simpson E M, Stewart A F, Teboul L, Tocchini Valentini G P, Valenzuela D, West A, Wurst W

机构信息

Institute of Developmental Genetics, Helmholtz Zentrum Muenchen, D-85764 Neuherberg, Germany.

Biotechnology Center (BIOTEC) of the Technische Universität Dresden, 01307 Dresden, Germany.

出版信息

Drug Discov Today Dis Models. 2016 Summer;20:3-12. doi: 10.1016/j.ddmod.2017.08.002. Epub 2017 Sep 12.

DOI:10.1016/j.ddmod.2017.08.002
PMID:39132094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11315453/
Abstract

The International Knockout Mouse Consortium (IKMC) developed high throughput gene trapping and gene targeting pipelines that produced mostly conditional mutations of more than 18,500 genes in C57BL/6N mouse embryonic stem (ES) cells which have been archived and are freely available to the research community as a frozen resource. From this unprecedented resource more than 6,000 mutant mouse strains have been produced by the IKMC and mostly the International Mouse Phenotyping Consortium (IMPC). In addition, a cre-driver resource was established including 250 inducible cre-driver mouse strains in a C57BL/6 background. Complementing the cre-driver resource, a collection of comprising 27 cre-driver rAAVs has also been produced. The resources can be easily accessed at the IKMC/IMPC web portal (www.mousephenotype.org). The IKMC/IMPC resource is a standardized reference library of mouse models with defined genetic backgrounds that enables the analysis of gene-disease associations in mice of different genetic makeup and should therefore have a major impact on biomedical research.

摘要

国际基因敲除小鼠联盟(IKMC)开发了高通量基因捕获和基因靶向流程,在C57BL/6N小鼠胚胎干细胞中产生了超过18500个基因的大多数条件性突变,这些细胞已存档,并作为冷冻资源免费提供给研究界。IKMC以及主要是国际小鼠表型分析联盟(IMPC)利用这一前所未有的资源培育出了6000多个突变小鼠品系。此外,还建立了一个cre驱动资源库,其中包括250个C57BL/6背景下的可诱导cre驱动小鼠品系。作为cre驱动资源的补充,还制备了一组包含27个cre驱动rAAV的集合。这些资源可在IKMC/IMPC门户网站(www.mousephenotype.org)上轻松获取。IKMC/IMPC资源是一个具有明确遗传背景的标准化小鼠模型参考库,能够分析不同基因组成小鼠中的基因-疾病关联,因此应该会对生物医学研究产生重大影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/8c389330f9ef/nihms-945349-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/3d6d790c7663/nihms-945349-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/660f8348ebc5/nihms-945349-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/3a80c883c0a5/nihms-945349-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/ff37a99286ad/nihms-945349-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/8c389330f9ef/nihms-945349-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/3d6d790c7663/nihms-945349-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/660f8348ebc5/nihms-945349-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/3a80c883c0a5/nihms-945349-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/ff37a99286ad/nihms-945349-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ca/11315453/8c389330f9ef/nihms-945349-f0006.jpg

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本文引用的文献

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Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.国际小鼠表型分析联盟从3328个基因敲除实验中发现疾病模型。
Nat Genet. 2017 Aug;49(8):1231-1238. doi: 10.1038/ng.3901. Epub 2017 Jun 26.
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Generation of a multipurpose mouse allele by targeted gene trapping.通过靶向基因捕获产生多用途小鼠等位基因。
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High-throughput discovery of novel developmental phenotypes.新型发育表型的高通量发现
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CRISPR-Cas9 enables conditional mutagenesis of challenging loci.CRISPR-Cas9 可实现具有挑战性的基因座的条件性突变。
Sci Rep. 2016 Sep 1;6:32326. doi: 10.1038/srep32326.
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Animal Models Are Valid to Uncover Disease Mechanisms.动物模型对于揭示疾病机制是有效的。
PLoS Genet. 2016 May 26;12(5):e1006013. doi: 10.1371/journal.pgen.1006013. eCollection 2016 May.
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Using the mouse to model human disease: increasing validity and reproducibility.利用小鼠对人类疾病进行建模:提高有效性和可重复性。
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