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Molecular cloning and characterization of five annexin genes from Indian mustard (Brassica juncea L. Czern and Coss)
Authors:Sravan Kumar Jami  Ahan Dalal  K Divya  PB Kirti
Institution:1. Post Graduate Department of Biotechnology, St. Xavier''s College (Autonomous), 30, Mother Teresa Sarani, Kolkata, 700016, West Bengal, India;2. Amity Institute of Organic Agriculture, Amity University, Noida, India;1. College of Horticulture, Shenyang Agricultural University, Shenyang 110866, China;2. Life Science and Technology Institute, Yangtze Normal University, Chongqing 408100, China;1. ICAR – Indian Institute of Agricultural Biotechnology, Ranchi 834 010, Jharkhand, India;2. ICAR – National Bureau of Plant Genetic Resources, Regional Station, Ranchi 834 010, Jharkhand, India;3. ICAR – Directorate of Rapeseed-Mustard Research, Bharatpur 321 303, Rajasthan, India;4. ICAR – National Bureau of Plant Genetic Resources, New Delhi 110 012, India;1. Department of Biochemistry, Nencki Institute of Experimental Biology, 3 Pasteur Street, PL-02093 Warsaw, Poland;2. Department of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, 3 Pasteur Street, PL-02093 Warsaw, Poland;3. Department of Experimental Design and Bioinformatics, Faculty of Agriculture and Biology, Warsaw University of Life Sciences, Nowoursynowska 166, 02-787 Warsaw, Poland
Abstract:Plant annexins constitute a multigene family having suggested roles in a variety of cellular processes including stress responses. We have isolated and characterized five different cDNAs of mustard, Brassica juncea (AnnBj1, AnnBj2, AnnBj3, AnnBj6 and AnnBj7) encoding annexin proteins using a RT-PCR/RACE-PCR based strategy. The predicted molecular masses of these annexins are ~36.0 kDa with acidic pIs. At the amino acid level, they share high sequence similarity with each other and with annexins from higher plants. Phylogenetic analysis revealed their evolutionary relationship with corresponding orthologous sequences in Arabidopsis and deduced proteins in various plant species. Expression analysis by semi-quantitative RT-PCR revealed that these genes are differentially expressed in various tissues. The expression patterns of these genes also showed regulation by various stress conditions such as exposure to signaling molecules, salinity and oxidative stress and wounding. Additionally, the in silico promoter analysis (of AnnBj1, AnnBj2 and AnnBj3) showed the presence of different cis-responsive elements that could respond to various stress conditions. These results indicate that AnnBj genes may play important roles in adaptation of plants to various environmental stresses.
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