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Cultured and Proteomic Evaluation of Resistance Powdery Mildew Near-isogenic Line Contained the H. villosum 6VS


Duan Shuang, Wang Lian, Gan Fu, Liu Xiaoying, Wang Zhenying, Peng Yongkang*
College of Life Science, Tianjin Normal University, Tianjin 300387, China
Abstract: In this study, we cultured a near-isogenic line (NIL) of Jing 411 and we are also evaluation the selection effects of near-isogenic line by proteomic techniques. Jing 411, which is a fine wheat variety but susceptible to powdery mildew pathogen, was crossed with wheat (H. villosum) chromosome translocation line 6AL/6VS. The donor of the resistance gene, F1 individuals then were back-crossed with Jing 411 seven times and selfed to produce progenice (NIL). The proteome of leaves and roots were investigated and the results indicated that 43.8% protein spots changed had a tendency to 6AL/6VS and 56.2% had a tendency to recurrent parent Jing 411 in leaves of NILS. In roots, 41.7% protein spots changed had a tendency to 6AL/6VS and 58.3% protein spots changed tended to recurrent parent Jing 411. 23 protein spots were identified by MS/MS. They were ATP synthase beta subunit, glycosyltransferase family 2 protein, Rab7/RabG-family small GTPase, COP1-Interacting protein 7, cryptochrome 1a, ribosomal protein L16, transcription initiation factor TFIID subunit, 23.5 kDa heat-shock protein, POR, RIC1, NBS-LRR resistance protein, transcription factor, serine/threonine-protein kinase haspin, F-actin capping protein beta subunit, mitochondrial protein translocase family, maturase K, NADH dehydrogenase subunit F, chloroplast Tha 4-2, mitochondrial translational initiation factor, ATP binding protein, SNF-1 related kinase, heat shock protein 70 and lipase family protein. The identified proteins were found to de involved in diverse biological processes, covering energy pathway, glucose-metabolism, signal transduction, photoreaction, DNA and RNA synthesis and defense response. Proteome technique can be used to evaluation the selection effect of NIL.


CSTR: 32200.14.cjcb.2012.06.0008