Development of a Brassica seed cDNA microarray

被引:17
|
作者
Xiang, Daoquan [1 ]
Datla, Raju [1 ]
Li, Fengling [1 ]
Cutler, Adrian [1 ]
Malik, Meghna R. [1 ]
Krochko, Joan E. [1 ]
Sharma, Nirmala [1 ]
Fobert, Pierre [1 ]
Georges, Fawzy [1 ]
Selvaraj, Gopalan [1 ]
Tsang, Ed [1 ]
Klassen, Darrin [1 ]
Koh, Chushin [1 ]
Deneault, Jean-Sebastien [2 ]
Nantel, Andre [2 ]
Nowak, Jacek [1 ]
Keller, Wilf [1 ]
Bekkaoui, Faouzi [1 ]
机构
[1] Natl Res Council Canada, Inst Plant Biotechnol, Saskatoon, SK S7N 0W9, Canada
[2] Natl Res Council Canada, Biotechnol Res Inst, Montreal, PQ H4P 2R2, Canada
关键词
Brassica; cDNA; microarray; seed; embryo; ESTs; gene expression;
D O I
10.1139/G07-115
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Brassica species represent several important crops including canola (Brassica napus). Understanding of genetic elements that contribute to seed-associated functions will impact future improvements in the canola crop. Brassica species share a very close taxonomic and molecular relationship with Arabidopsis thaliana. However, there are several subtle but distinct seed-associated agronomic characteristics that differ among the oil seed crop species. To address these, we have generated 67 535 ESTs predominately from Brassica seeds, analyzed these sequences, and identified 10 642 unigenes for the preparation of a targeted seed cDNA array. A set of 10642 PCR primer pairs was designed and corresponding amplicons were produced for spotting, along with relevant controls. Critical quality control tests produced satisfactory results for use of this microarray in biological experiments. The microarray was also tested with specific RNA targets from embryos, germinating seeds, and leaf tissues. The hybridizations, signal intensities, and overall quality of these slides were consistent and reproducible. Additionally, there are 429 ESTs represented on the array that show no homology with any A. thaliana annotated gene or any gene in the Brassica genome databases or other plant databases; however, all of these probes hybridized to B. napus transcripts, indicating that the array also will be useful in defining expression patterns for genes so far unique to Brassica species.
引用
收藏
页码:236 / 242
页数:7
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