Popp Michael P, Liu Li, Timmers Adrian, Esson Douglas W, Shiroma Lineu, Meyers Craig, Berceli Scott, Tao Ming, Wistow Graeme, Schultz Gregory S, Sherwood Mark B
University of Florida's Interdisciplinary Center for Biotechnology Research, University of Florida, Gainsville, FL 32610-0294, USA.
Mol Vis. 2007 Feb 2;13:164-73.
To develop a microarray for the rabbit that can be used for ocular gene expression research.
Messenger RNA was isolated from anterior segment tissues (cornea, conjunctiva, and iris) and posterior segment tissues (lens, retina, and sclera) of rabbit eyes and used to create two independent cDNA libraries through the NEIBank project. Clones from each of these libraries were sequenced from both the 5' and 3' ends. These sequences and those from the National Center for Biotechnology Information (NCBI) taxonomy database for rabbit were combined and electronically assembled into a set of unique nonoverlapping continuous sequences (contigs). For each contig, a homology search was performed using BLASTX and BLASTN against both the NCBI NR and NT databases to provide gene annotation. Unique contigs were sent to Agilent Technologies, where 60 base oligonucleotide probes were designed and synthesized, in situ, on two different arrays in an 8 array x 1900 element format. Glaucoma filtration surgery was performed on one eye of six rabbits. After 14 days, tissue was harvested from the conjunctiva and Tenon's capsule of both the surgically treated and untreated control eyes. Total RNA from each sample was labeled with cyanine dyes and hybridized to our custom microarrays.
Of the 3,154 total probes present on the two arrays, 2,522 had a signal value above the background. The expression of 315 genes was significantly altered by glaucoma filtration surgery. Genes whose expression was altered included proteins associated with inflammatory response, defense response, and proteins involved in synthesis of the extracellular matrix.
The results of this rabbit microarray study are consistent with those from other wound healing studies, indicating that this array can provide valid information on broad patterns of gene expression. This is the first microarray available for rabbit studies and is a valuable tool that can be used to study molecular events in the eye.
开发一种可用于兔眼基因表达研究的微阵列。
从兔眼前节组织(角膜、结膜和虹膜)和后节组织(晶状体、视网膜和巩膜)中分离信使核糖核酸,并通过NEIBank项目用于创建两个独立的互补脱氧核糖核酸文库。对这些文库中的每个克隆进行5'端和3'端测序。将这些序列与来自美国国立生物技术信息中心(NCBI)兔分类数据库的序列合并,并通过电子方式组装成一组独特的非重叠连续序列(重叠群)。对于每个重叠群,使用BLASTX和BLASTN在NCBI NR和NT数据库中进行同源性搜索以提供基因注释。将独特的重叠群发送给安捷伦科技公司,在那里以8阵列×1900元件的格式在两种不同的阵列上原位设计并合成60碱基的寡核苷酸探针。对6只兔的一只眼睛进行青光眼滤过手术。14天后,从手术治疗和未治疗的对照眼的结膜和Tenon囊收集组织。每个样品的总核糖核酸用花青染料标记,并与我们定制的微阵列杂交。
两个阵列上共有的3154个探针中,2522个的信号值高于背景。青光眼滤过手术使315个基因的表达发生显著改变。表达发生改变的基因包括与炎症反应、防御反应相关的蛋白质以及参与细胞外基质合成的蛋白质。
这项兔微阵列研究的结果与其他伤口愈合研究的结果一致,表明该阵列可以提供关于基因表达广泛模式的有效信息。这是首个可用于兔研究的微阵列,是一种可用于研究眼部分子事件的有价值工具。