Mr. Baolong Zhang, Dr. Wanchao Ni, Ms. Yuwen Yang, and Dr. Xinlian Shen. Institute of Agro-biotechnology, Jiangsu Academy of Agricultural Sciences, Zhongling Street 50, Nanjing, China
Cotton diseases represent a major challenge to cotton growth. Cloning of cotton pathogen response gene and promoter was of great importance for us to improve disease resistance. In this study, a full length CC-NBS-LRR gene (GHNBS) and its 5´ flanking sequence have been cloned by race and tail PCR and further studied. The entire coding region is 2583bp and encodes a polypeptide of 861 amino acids with 28% maximum homology to an R gene of Arabidopsis deposited in the GenBank. Semi Quantitative RT-PCR showed GHNBS expressed in floral bud, petal, phloem, root and leaf and has a more expression pattern in root and leaf. The 5′ flanking sequence of GHNBS contained CAAT-box, TATA-box, several pathogen, SA, MeJA and ethylene responsive elements by PLACE analysis. Different 5′ promoter deletion derivatives with the coding region of the GUS gene fusions were transformed into Arabidopsis. Histochemical localization showed strong staining in roots, phenol of the stem and leave vein. GHNBS promoter was up regulated after SA, ABA, MeJA, ethylene and Pathogen DC3000 treatments.