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MOLECULAR CLONING OF TWO NOVEL RICE CDNA SEQUENCES ENCODING PUTATIVE CALCIUM-DEPENDENT PROTEIN KINASES

机译:编码钙依赖性蛋白激酶的两种新水稻CDNA序列的分子克隆

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We have isolated, from a cDNA library constructed from rice coleoptiles, two sequences, OSCPK2 and OSCPK11, that encode for putative calcium-dependent protein kinase (CDPK) proteins. OSCPK2 and OSCPK11 cDNAs are related to SPK, another gene encoding a rice CDPK that is specifically expressed in developing seeds [20]. OSCPK2 and OSCPK11-predicted protein sequences are 533 and 542 amino acids (aa) long with a corresponding molecular mass of 59436 and 61079 Da respectively. Within their polypeptide chain, they all contain those conserved features that define a plant CDPK; kinase catalytic sequences are linked to a calmodulin-like regulatory domain through a junction region. The calmodulinlike regulatory domain of the predicted OSCPK2 protein contains 4 EF-hand calcium-binding sites while OSCPK11 has conserved just one canonical EF-hand motif. In addition, OSCPK2- and OSCPK11-predicted proteins contain, at their N-terminal region preceding the catalytic domain, a stretch of 80 or 74 residues highly rich in hydrophilic amino acids. Comparison of the NH2-terminal sequence of all three rice CDPKs so far identified (OSCPK2, OSCPK11 and SPK) indicates the presence of a conserved MGxxC(S/Q)xxT motif that may define a consensus signal for N-myristoylation. OSCPK2 and OSCPK11 proteins are both encoded by a single-copy gene and their polyadenylated transcripts are 2.4 and 3.5 kb long respectively. OSCPK2 and OSCPK11 mRNAs are equally abundant in rice roots and coleoptiles. A 12 h white light treatment of the coleoptiles reduces the amount of OSCPK2 mRNA with only a slight effect on the level of OSCPK11 transcript. With anoxic treatments, OSCPK2 mRNA level declined significantly and promptly while the amount of OSCPK11 transcript remained constant. [References: 48]
机译:我们从水稻胚芽鞘构建的cDNA文库中,分离出两个序列OSCPK2和OSCPK11,它们编码假定的钙依赖性蛋白激酶(CDPK)蛋白。 OSCPK2和OSCPK11 cDNA与SPK有关,SPK是另一种编码水稻CDPK的基因,在发育中的种子中特异性表达[20]。 OSCPK2和OSCPK11预测的蛋白质序列长533和542个氨基酸(aa),相应的分子量分别为59436和61079 Da。在它们的多肽链中,它们都包含那些定义植物CDPK的保守特征;激酶催化序列通过连接区与钙调蛋白样调节域相连。预测的OSCPK2蛋白的钙调蛋白样调节域包含4个EF手钙结合位点,而OSCPK11仅保守了一个规范的EF手基序。此外,OSCPK2和OSCPK11预测的蛋白质在其催化结构域之前的N端区域包含一段80或74个高度富含亲水性氨基酸的残基。到目前为止确定的所有三个水稻CDPK(OSCPK2,OSCPK11和SPK)的NH2-末端序列的比较表明存在保守的MGxxC(S / Q)xxT基序,该基序可以定义N-豆蔻酰化的共有信号。 OSCPK2和OSCPK11蛋白均由单拷贝基因编码,它们的多聚腺苷酸转录物分别长2.4 kb和3.5 kb。 OSCPK2和OSCPK11 mRNA在水稻根和胚芽鞘中同样丰富。胚芽鞘的12 h白光处理减少了OSCPK2 mRNA的量,而对OSCPK11转录物的水平仅有轻微影响。缺氧处理后,OSCPK2 mRNA水平显着下降,并迅速下降,而OSCPK11转录物的量保持恒定。 [参考:48]

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