Scearce L Marie, Brestelli John E, McWeeney Shannon K, Lee Catherine S, Mazzarelli Joan, Pinney Deborah F, Pizarro Angel, Stoeckert Christian J, Clifton Sandra W, Permutt M Alan, Brown Juliana, Melton Douglas A, Kaestner Klaus H
Department of Genetics, University of Pennsylvania, 415 Curie Boulevard, Philadephia, PA 19104, USA.
Diabetes. 2002 Jul;51(7):1997-2004. doi: 10.2337/diabetes.51.7.1997.
Over the past 5 years, microarrays have greatly facilitated large-scale analysis of gene expression levels. Although these arrays were not specifically geared to represent tissues and pathways known to be affected by diabetes, they have been used in both type 1 and type 2 diabetes research. To prepare a tool that is particularly useful in the study of type 1 diabetes, we have assembled a nonredundant set of 3,400 clones representing genes expressed in the mouse pancreas or pathways known to be affected by diabetes. We have demonstrated the usefulness of this clone set by preparing a cDNA glass microarray, the PancChip, and using it to analyze pancreatic gene expression from embryonic day 14.5 through adulthood in mice. The clone set and corresponding array are useful resources for diabetes research.
在过去5年中,微阵列极大地推动了基因表达水平的大规模分析。尽管这些阵列并非专门用于呈现已知受糖尿病影响的组织和通路,但它们已被用于1型和2型糖尿病研究。为了制备一种在1型糖尿病研究中特别有用的工具,我们汇集了一组3400个非冗余克隆,这些克隆代表了在小鼠胰腺中表达的基因或已知受糖尿病影响的通路。我们通过制备一种cDNA玻璃微阵列——胰腺芯片(PancChip),并使用它来分析从小鼠胚胎第14.5天到成年期的胰腺基因表达,证明了该克隆集的实用性。该克隆集和相应的阵列是糖尿病研究的有用资源。