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Transcriptome Profiling of Dehydration Stress in the Chinese Cabbage (Brassica rapa L. ssp pekinensis) by Tag Sequencing

文献类型： 外文期刊

作者： Yu, Shuancang 1 ; Zhang, Fenglan 1 ; Yu, Yangjun 1 ; Zhang, Deshuang 1 ; Zhao, Xiuyun 1 ; Wang, Wenhong 1 ;

作者机构： 1.BAAFS, BVRC, Beijing 100097, Peoples R China

关键词： Brassica rapa;Dehydration stress;Transcriptome profiling;Solexa Illumina;Tag sequencing

期刊名称：PLANT MOLECULAR BIOLOGY REPORTER （ 影响因子：1.595； 五年影响因子：2.042 ）

ISSN：

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收录情况： SCI

摘要： Chinese cabbage (Brassica rapa L. ssp. pekinensis) is a vegetable crop with high water requirement and is adversely affected by drought during cultivation. A genome-wide transcription analysis in response to drought is essential to provide effective genetic engineering strategies to improve stress tolerance in crop plants. To gain a deeper understanding of the mechanisms of drought tolerance in B. rapa, we conducted the first genome-wide analysis of gene expression during a drought model using tag sequencing with a Solexa Illumina array. Leaf samples at four time points, 0 day, 1 day, 2 days, and 3 days after dehydration treatment, were taken from a B. rapa DH line, T12-19, and the corresponding RNA was used to construct the expression libraries. The total number of tags per library ranged from 5.6 to 7.6 million and, among these, 13,036, 12,472, 12,774, and 12,227 distinct clean tags for the four respective libraries were unambiguously mapped to a publicly available unigene database. The analysis of differentially expressed genes revealed that 1,092 genes were significantly altered in response to water deficit. In this set of genes, we found 37 transcription factors, 28 genes involved in signal transduction, and 61 water- and osmosensing-responsive genes. Overall, the tag sequencing analyses demonstrated a high degree of transcriptional complexity in response to dehydration stress and represents a considerable improvement over microarray data in the large-scale analysis of transcriptional changes.

  • 相关文献

[1]Cloning and expression profiling of the PacSnRK2 and PacPP2C gene families during fruit development, ABA treatment, and dehydration stress in sweet cherry. Shen, Xinjie,Zhao, Wei,Shen, Xinjie,Guo, Xiao,Zhao, Di,Wang, Yantao,Peng, Xiang,Wei, Yan,Zhai, Zefeng,Li, Tianhong,Zhang, Qiang,Jiang, Yuzhuang,Li, Tianhong. 2017

[2]A semi-fertile interspecific hybrid of Brassica rapa and B. nigra and the cytogenetic analysis of its progeny. Sheng, Xiaoguang,Wen, Guiju,Zhao, Hong,Liu, Fan,Sheng, Xiaoguang,Wen, Guiju,Guo, Yangdong,Yan, Hong. 2012

[3]Regulation of bolting and identification of the alpha-tubulin gene family in Brassica rapa L. ssp pekinensis. Zhang, Y. W.,Jin, D.,Xu, C.,Zhang, L.,Guo, M. H.,Zhang, Y. W.,Fang, Z. Y.. 2016

[4]An Improved Brassica rapa Genetic Linkage Map and Locus-specific Variations in a Doubled Haploid Population. Yu, Shuancang,Zhang, Fenglan,Zhao, Xiang,Yu, Yangjun,Zhang, Deshuang,Zhao, Xiuyun,Wang, Weihong.

[5]Mapping the BrPur gene for purple leaf color on linkage group A03 of Brassica rapa. Wang, Weihong,Zhang, Deshuang,Yu, Shuancang,Liu, Jin,Wang, Dan,Zhang, Fenglan,Yu, Yangjun,Zhao, Xiuyun,Lu, Guixiang,Su, Tongbing,Wang, Weihong,Zhang, Deshuang,Yu, Shuancang,Liu, Jin,Wang, Dan,Zhang, Fenglan,Yu, Yangjun,Zhao, Xiuyun,Lu, Guixiang,Su, Tongbing.

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