Chen Xiaofeng, Hou Xilin, Zhang Jingyi, Zheng Jiaqiu
State Key Laboratory of Crop Genetics and Germplasm Enhancement, College of Horticulture, Nanjing Agricultural University, 6 Tongwei Road, Nanjing, 210095, PR China.
Mol Biol Rep. 2008 Dec;35(4):621-9. doi: 10.1007/s11033-007-9132-0. Epub 2007 Aug 31.
Two cDNA clones for a pathogen induced genes in non-heading Chinese cabbage (Brassica rapa ssp. chinensis L. cv. Suzhouqing) were isolated and characterized. The two full-length cDNA clones, designated Bcchi and BcAF were isolated during the resistance response to Peronospora parasitica. Sequence analysis of corresponding cDNA clones confirmed the translation products of both genes showed high degree of homology to other plant chitinases and plant defensins, respectively. Genomic DNA Southern blot analysis indicated that each gene represented a small multi-gene family. Upon inoculation with P. parasitica, both genes transcripts were rapid accumulated in the infected leaves. Tissue-specific expression of both genes showed that 24 h post-inoculation the highest expression tissue of Bcchi mRNA was leaves, and 12 h post-inoculation the highest expression tissue of BcAF mRNA was leaves. These data revealed that both genes may be involved in plant resistance against fungal pathogen infection.
分离并鉴定了两个与不结球白菜(Brassica rapa ssp. chinensis L. cv. Suzhouqing)中病原菌诱导基因相关的cDNA克隆。这两个全长cDNA克隆分别命名为Bcchi和BcAF,是在对寄生霜霉(Peronospora parasitica)的抗性反应过程中分离得到的。对相应cDNA克隆的序列分析证实,这两个基因的翻译产物分别与其他植物几丁质酶和植物防御素具有高度同源性。基因组DNA Southern杂交分析表明,每个基因都代表一个小的多基因家族。接种寄生霜霉后,两个基因的转录本在感染叶片中迅速积累。两个基因的组织特异性表达表明,接种后24小时,Bcchi mRNA表达量最高的组织是叶片,接种后12小时,BcAF mRNA表达量最高的组织是叶片。这些数据表明,这两个基因可能都参与了植物对真菌病原菌感染的抗性反应。