کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2818083 | 1160029 | 2012 | 7 صفحه PDF | دانلود رایگان |
The various iterations of the HapMap Project and many genome-wide association studies (GWAS) have identified hundreds of potential genes involved in monogenic and multifactorial traits. We constructed an arrayed 115,000-member human genomic library in the PAC shuttle vector pJCPAC-Mam2 that can be propagated in both bacterial and human cells. The library appears to represent a two-fold coverage of the human genome. Transient transfection of a p53-containing PAC clone into p53-null Saos-2 human osteosarcoma cells demonstrated that both p53 mRNA and protein were produced. Additionally, expression of the p53 protein triggered apoptosis in a subset of the Saos-2 cells. This library should serve as a valuable resource to validate potential disease genes identified by GWAS in human cell lines and in animal models. Also, individual library members could potentially be used for gene therapy trials for a variety of recessive disorders.
► Human genomic PAC library for functional genomics.
► p53-containing PAC clone is transcribed in p53 null Saos-2 cells.
► p53-containing PAC clone is translated in p53 null Saos-2 cells.
► p53-containing PAC clone causes apoptosis in p53 null Saos-2 cells.
► Human genomic PAC library for gene therapy.
Journal: Gene - Volume 496, Issue 2, 1 April 2012, Pages 103–109