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Genome-wide analysis of lectin receptor-like kinase family from Arabidopsis and rice 总被引:2,自引:0,他引:2
Lectin receptor-like kinases (LecRLKs) are class of membrane proteins found in higher plants that are involved in diverse functions ranging from plant growth and development to stress tolerance. The basic structure of LecRLK protein comprises of a lectin and a kinase domain, which are interconnected by transmembrane region. Here we have identified LecRLKs from Arabidopsis and rice and studied these proteins on the basis of their expression profile and phylogenies. We were able to identify 32 G-type, 42 L-type and 1 C-type LecRLKs from Arabidopsis and 72 L-type, 100 G-type and 1 C-type LecRLKs from rice on the basis of their annotation and presence of lectin as well kinase domains. The whole family is rather intron-less. We have sub-grouped the gene family on the basis of their phylogram. Although on the basis of sequence the members of each group are closely associated but their functions vary to a great extent. The interacting partners and coexpression data of the genes revealed the importance of gene family in physiology and stress related responses. An in-depth analysis on gene-expression suggested clear demarcation in roles assigned to each gene. To gain additional knowledge about the LecRLK gene family, we searched for previously unreported motifs and checked their importance structurally on the basis of homology modelling. The analysis revealed that the gene family has important roles in diverse functions in plants, both in the developmental stages and in stress conditions. This study thus opens the possibility to explore the roles that LecRLKs might play in life of a plant. 相似文献
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Expansion of the receptor-like kinase/Pelle gene family and receptor-like proteins in Arabidopsis 总被引:21,自引:0,他引:21
Receptor-like kinases (RLKs) are a family of transmembrane proteins with versatile N-terminal extracellular domains and C-terminal intracellular kinases. They control a wide range of physiological responses in plants and belong to one of the largest gene families in the Arabidopsis genome with more than 600 members. Interestingly, this gene family constitutes 60% of all kinases in Arabidopsis and accounts for nearly all transmembrane kinases in Arabidopsis. Analysis of four fungal, six metazoan, and two Plasmodium sp. genomes indicates that the family was represented in all but fungal genomes, indicating an ancient origin for the family with a more recent expansion only in the plant lineages. The RLK/Pelle family can be divided into several subfamilies based on three independent criteria: the phylogeny based on kinase domain sequences, the extracellular domain identities, and intron locations and phases. A large number of receptor-like proteins (RLPs) resembling the extracellular domains of RLKs are also found in the Arabidopsis genome. However, not all RLK subfamilies have corresponding RLPs. Several RLK/Pelle subfamilies have undergone differential expansions. More than 33% of the RLK/Pelle members are found in tandem clusters, substantially higher than the genome average. In addition, 470 of the RLK/Pelle family members are located within the segmentally duplicated regions in the Arabidopsis genome and 268 of them have a close relative in the corresponding regions. Therefore, tandem duplications and segmental/whole-genome duplications represent two of the major mechanisms for the expansion of the RLK/Pelle family in Arabidopsis. 相似文献
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Phylogenomic analysis of the receptor-like proteins of rice and Arabidopsis 总被引:6,自引:0,他引:6 下载免费PDF全文
The tomato (Lycopersicon esculentum) Cf-9 resistance gene encodes the first characterized member of the plant receptor-like protein (RLP) family. Other RLPs such as CLAVATA2 and TOO MANY MOUTHS are known to regulate development. The domain structure of RLPs consists of extracellular leucine-rich repeats, a transmembrane helix, and a short cytoplasmic region. Here, we identify 90 RLPs in rice (Oryza sativa) and compare them with functionally characterized RLPs from different plant species and with 56 Arabidopsis (Arabidopsis thaliana) RLPs, including the downy mildew resistance protein RPP27. Many RLPs cluster into four distinct superclades, three of which include RLPs known to be involved in plant defense. Sequence comparisons reveal diagnostic amino acid residues that may specify different molecular functions in different RLP subtypes. This analysis of rice RLPs thus identified at least 73 candidate resistance genes and four genes potentially involved in development. Due to the synteny between rice and other Gramineae, this analysis should provide valuable tools for experimental studies in rice and other cereals. 相似文献
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Some SERK-family receptor-like protein kinase genes have been shown to confer embryonic competence to cells. In this study, we isolated two novel rice genes, OsSERK1 and OsSERK2, belonging to the SERK-family. OsSERK2 showed constitutive expression. The OsSERK1 promoter showed reporter gene activities in some specific tissues in a germinating seed, leaf and root, but not in a developing embryo. This promoter activity suggests that OsSERK1 may have roles in non-embryonic tissues rather than in the embryo. 相似文献
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Pavan Umate 《Plant signaling & behavior》2011,6(3):335-338
The enzymes called lipoxygenases (LOXs) can dioxygenate unsaturated fatty acids, which leads to lipoperoxidation of biological membranes. This process causes synthesis of signaling molecules and also leads to changes in cellular metabolism. LOXs are known to be involved in apoptotic (programmed cell death) pathway, and biotic and abiotic stress responses in plants. Here, the members of LOX gene family in Arabidopsis and rice are identified. The Arabidopsis and rice genomes encode 6 and 14 LOX proteins, respectively, and interestingly, with more LOX genes in rice. The rice LOXs are validated based on protein alignment studies. This is the first report wherein LOXs are identified in rice which may allow better understanding the initiation, progression and effects of apoptosis, and responses to bitoic and abiotic stresses and signaling cascades in plants.Key words: apoptosis, biotic and abiotic stresses, genomics, jasmonic acid, lipidsLipoxygenases (linoleate:oxygen oxidoreductase, EC 1.13.11.-; LOXs) catalyze the conversion of polyunsaturated fatty acids (lipids) into conjugated hydroperoxides. This process is called hydroperoxidation of lipids. LOXs are monomeric, non-heme and non-sulfur, but iron-containing dioxygenases widely expressed in fungi, animal and plant cells, and are known to be absent in prokaryotes. However, a recent finding suggests the existence of LOX-related genomic sequences in bacteria but not in archaea.1 The inflammatory conditions in mammals like bronchial asthama, psoriasis and arthritis are a result of LOXs reactions.2 Further, several clinical conditions like HIV-1 infection,3 disease of kidneys due to the activation of 5-lipoxygenase,4,5 aging of the brain due to neuronal 5-lipoxygenase6 and atherosclerosis7 are mediated by LOXs. In plants, LOXs are involved in response to biotic and abiotic stresses.8 They are involved in germination9 and also in traumatin and jasmonic acid biochemical pathways.10,11 Studies on LOX in rice are conducted to develop novel strategies against insect pests12 in response to wounding and insect attack,13 and on rice bran extracts as functional foods and dietary supplements for control of inflammation and joint health.14 In Arabidopsis, LOXs are studied in response to natural and stress-induced senescence,15 transition to flowering,16 regulation of lateral root development and defense response.17The arachidonic, linoleic and linolenic acids can act as substrates for different LOX isozymes. A hydroperoxy group is added at carbons 5, 12 or 15, when arachidonic acid is the substrate, and so the LOXs are designated as 5-, 12- or 15-lipoxygenases. Sequences are available in the database for plant lipoxygenases (EC:1.13.11.12), mammalian arachidonate 5-lipoxygenase (EC:1.13.11.34), mammalian arachidonate 12-lipoxygenase (EC:1.13.11.31) and mammalian erythroid cell-specific 15-lipoxygenase (EC:1.13.11.33). The prototype member for LOX family, LOX-1 of Glycine max L. (soybean) is a 15-lipoxygenase. The LOX isoforms of soybean (LOX-1, LOX-2, LOX-3a and LOX-3b) are the most characterized of plant LOXs.18 In addition, five vegetative LOXs (VLX-A, -B, -C, -D, -E) are detected in soybean leaves.19 The 3-dimensional structure of soybean LOX-1 has been determined.20,21 LOX-1 was shown to be made of two domains, the N-terminal domain-I which forms a β-barrel of 146 residues, and a C-terminal domain-II of bundle of helices of 693 residues21 (Fig. 1). The iron atom was shown to be at the centre of domain-II bound by four coordinating ligands, of which three are histidine residues.22Open in a separate windowFigure 1Three-dimensional structure of soybean lipoxygenase L-1. The domain I (N-terminal) and domain II (C-terminal) are indicated. The catalytic iron atom is embedded in domain II (PDB ID-1YGE).21This article describes identification of LOX genes in Arabidopsis and rice. The Arabidopsis genome encodes for six LOX proteins23 (www.arabidopsis.org) (Locus Annotation Nomenclature A* B* C* AT1G55020 lipoxygenase 1 (LOX1) LOX1 859 98044.4 5.2049 AT1G17420 lipoxygenase 3 (LOX3) LOX3 919 103725.1 8.0117 AT1G67560 lipoxygenase family protein LOX4 917 104514.6 8.0035 AT1G72520 lipoxygenase, putative LOX6 926 104813.1 7.5213 AT3G22400 lipoxygenase 5 (LOX5) LOX5 886 101058.8 6.6033 AT3G45140 lipoxygenase 2 (LOX2) LOX2 896 102044.7 5.3177