Yan Xiaoyan, Sablok Gaurav, Feng Gang, Ma Jiaxin, Zhao Hongwei, Sun Xiaoyong
Affiliated Hospital of Shandong University of Traditional Chinese Medicine, No. 42 Wenhua West Road, Jinan, Shandong 250011, China.
Plant Functional Biology and Climate Change Cluster (C3), University of Technology Sydney, PO Box 123, Broadway, NSW 2007, Australia.
FEBS Lett. 2015 Jul 8;589(15):1766-70. doi: 10.1016/j.febslet.2015.05.029. Epub 2015 May 27.
Regulation of proteome diversity by alternative splicing has been widely demonstrated in plants and animals. NAGNAG splicing, which was recently defined as a tissue specific event, results in the production of two distinct isoforms that are distinguished by three nucleotides (NAG) as a consequence of the intron proximal or distal to the splice site. Since the NAGNAG mechanism is not well characterized, tools for the identification and quantification of NAGNAG splicing events remain under-developed. Here we report nagnag, an R-based NAGNAG splicing detection tool, which accurately identifies and quantifies NAGNAG splicing events using RNA-Seq. Overall, nagnag produces user-friendly visualization reports and highlights differences between the DNA/RNA/protein across the identified isoforms of the reported gene. The package is available on https://sourceforge.net/projects/nagnag/files/; or http://genome.sdau.edu.cn/research/software/nagnag.html.
可变剪接对蛋白质组多样性的调控已在植物和动物中得到广泛证实。NAGNAG剪接最近被定义为一种组织特异性事件,由于剪接位点近端或远端的内含子,会产生两种由三个核苷酸(NAG)区分的不同异构体。由于NAGNAG机制尚未得到充分表征,用于识别和定量NAGNAG剪接事件的工具仍未得到充分开发。在这里,我们报告了nagnag,一种基于R的NAGNAG剪接检测工具,它使用RNA测序准确识别和定量NAGNAG剪接事件。总体而言,nagnag生成用户友好的可视化报告,并突出显示所报告基因的已识别异构体之间DNA/RNA/蛋白质的差异。该软件包可在https://sourceforge.net/projects/nagnag/files/; 或http://genome.sdau.edu.cn/research/software/nagnag.html上获取。