Stage-specific gene expression during urediniospore germination in Puccinia striiformis f. sp tritici

Yonghong Zhang¹ , Zhipeng Qu¹ , Wenming Zheng² , Bo Liu¹ , Xiaojie Wang¹ , Xiaodan Xue¹ , Liangsheng Xu³ , Lili Huang¹ , Qingmei Han¹ , Jie Zhao¹ and Zhensheng Kang¹

¹College of Plant Protection and Shaanxi Key Laboratory of Molecular Biology for Agriculture, Northwest A&F University, Yangling, Shaanxi, 712100, P.R. China

²College of Life Sciences, Henan Agriculture University, Zhengzhou, Henan, 450002, P.R. China

³College of Life Sciences, Northwest A&F University, Yangling, Shaanxi, 712100, P.R. China

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BMC Genomics 2008, 9:203doi:10.1186/1471-2164-9-203


Published:	1 May 2008

Additional files

Additional file 1:

The redundancy of P. striiformis f. sp tritici ESTs derived from the germinated urediniospore cDNA library. The number of contigs consisting of 1, 2, 3–5, 6–10, 11–35, and more than 36 ESTs was presented by the columns.

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Additional file 2:

The most abundant ESTs identified in the P. striiformis f. sp. tritici germinated urediniospore library. These data provided represent the nine most abundant expressed ESTs.

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Additional file 3:

Uniseqs with significant homology to genes from different organisms. These data provided display the number of uniseqs have homology to genes from diversity organisms.

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Additional file 4:

Uniseqs with similarity (BLASTX, E-value < 10-5 or InterProScan, E-value < 10-5) to proteins in public databases were grouped into functional categories according to Gene Ontology. These data provided represent the original EST number and best hit.

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Additional file 5:

Sequences of primers and probes used for qRT-PCR. The primer pairs, probes and reference sequences used for qRT-PCR were listed.

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