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通过亚家族特异性LINE-1-PCR对LINE-1元件亚家族进行靶向克隆。

Targeted cloning of a subfamily of LINE-1 elements by subfamily-specific LINE-1-PCR.

作者信息

Casavant N C, Hardies S C

机构信息

Department of Biochemistry, University of Texas Health Science Center, San Antonio 78284-7760.

出版信息

Mamm Genome. 1993;4(4):193-201. doi: 10.1007/BF00417562.

Abstract

Subfamily-specific LINE-1 PCR (SSL1-PCR) is the targeted amplification and cloning of defined subfamilies of LINE-1 elements and their flanking sequences. The targeting is accomplished by incorporating a subfamily-specific sequence difference at the 3' end of a LINE-1 PCR primer and pairing it with a primer to an anchor ligated within the flanking region. SSL1-PCR was demonstrated by targeting amplification of a Mus spretus-specific LINE-1 subfamily. The amplified fragments were cloned to make an SSL1-PCR library, which was found to be 100-fold enriched for the targeted elements. PCR primers were synthesized based on the sequence flanking the LINE-1 element of four different clones. Three of the clones were recovered from Mus spretus DNA. A fourth clone was recovered from a congenic mouse containing both Mus spretus and Mus domesticus DNA. Amplification between these flanking primers and LINE-1 PCR primers produced a product in Mus spretus and not in Mus domesticus. These dimorphisms were further verified to be due to insertion of Mus spretus-specific LINE-1 elements into Mus spretus DNA and not into Mus domesticus DNA.

摘要

亚家族特异性LINE-1聚合酶链反应(SSL1-PCR)是对LINE-1元件的特定亚家族及其侧翼序列进行靶向扩增和克隆。靶向是通过在LINE-1聚合酶链反应引物的3'端引入亚家族特异性序列差异,并将其与侧翼区域内连接的锚定引物配对来实现的。通过靶向扩增小家鼠特异性LINE-1亚家族证明了SSL1-PCR。将扩增片段克隆以构建SSL1-PCR文库,发现该文库中靶向元件的富集度提高了100倍。基于四个不同克隆的LINE-1元件侧翼序列合成了聚合酶链反应引物。其中三个克隆从小家鼠DNA中回收。第四个克隆从同时含有小家鼠和家鼠DNA的近交系小鼠中回收。这些侧翼引物与LINE-1聚合酶链反应引物之间的扩增在小家鼠中产生了产物,而在家鼠中没有。进一步证实这些多态性是由于小家鼠特异性LINE-

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