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大鼠中可遗传且稳定的基因敲低

Heritable and stable gene knockdown in rats.

作者信息

Dann Christina Tenenhaus, Alvarado Alma L, Hammer Robert E, Garbers David L

机构信息

The Cecil H. and Ida Green Center for Reproductive Biology Sciences, Department of Pharmacology, University of Texas Southwestern Medical Center, 6001 Forest Park Road, Dallas, TX 75390-9051, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Jul 25;103(30):11246-51. doi: 10.1073/pnas.0604657103. Epub 2006 Jul 14.

Abstract

The rat has served as an excellent model for studies on animal physiology and as a model for human diseases such as diabetes and alcoholism; however, genetic studies have been limited because of the inability to knock out genes. Our goal was to produce heritable deficiencies in specific gene function in the rat using RNA interference to knock down gene expression in vivo. Lentiviral-mediated transgenesis was used to produce rats expressing a short hairpin RNA targeting Dazl, a gene expressed in germ cells and required for fertility in mice. Germ-line transmission of the transgene occurred, and its expression correlated with significant reductions in DAZL protein levels and male sterility, and the knockdown was stable over multiple generations (F(1)-F(3)). This study demonstrates an efficient system by which directed reverse genetic analysis can now be performed in the rat.

摘要

大鼠一直是动物生理学研究的优秀模型,也是糖尿病和酗酒等人类疾病的模型;然而,由于无法敲除基因,基因研究受到了限制。我们的目标是利用RNA干扰在体内敲低基因表达,从而在大鼠中产生特定基因功能的可遗传缺陷。慢病毒介导的转基因技术被用于培育表达靶向Dazl的短发夹RNA的大鼠,Dazl是一种在生殖细胞中表达且对小鼠生育力必需的基因。转基因发生了种系传递,其表达与DAZL蛋白水平的显著降低和雄性不育相关,并且这种敲低在多代(F(1)-F(3))中是稳定的。这项研究证明了一种有效的系统,通过该系统现在可以在大鼠中进行定向反向遗传分析。

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