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Identification and organization of chloroplastic and cytosolic l-myo-inositol 1-phosphate synthase coding gene(s) in Oryza sativa: comparison with the wild halophytic rice, Porteresia coarctata

机译:稻中叶绿体和胞质1-肌醇1-磷酸合酶编码基因的鉴定和组织:与野生盐生水稻,Porteresia coarctata的比较

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摘要

The gene coding for rice chloroplastic l-myo-inositol-1-phosphate synthase (MIPS; EC 5.5.1.4) has been identified by matrix-assisted laser desorption time-of-flight mass spectrometry analysis of the purified and immunologically cross-reactive ~60 kDa chloroplastic protein following two-dimensional polyacrylamide gel electrophoresis, which exhibited sequence identity with the cytosolic MIPS coded by OsINO1-1 gene. A possible chloroplastic transit peptide sequence was identified upstream of the OsINO1-1 gene upon analysis of rice genome. RT-PCR and confocal microscope studies confirmed transcription, effective translation and its functioning as a chloroplast transit peptide. Bioinformatic analysis mapped the chloroplastic MIPS (OsINO1-1) gene on chromosome 3, and a second MIPS gene (OsINO1-2) on chromosome 10 which lacks conventional chloroplast transit peptide sequence as in OsINO1-1. Two new PcINO1 genes, with characteristic promoter activity and upstream cis-elements were identified and cloned, but whether these proteins can be translocated to the chloroplast or not is yet to be ascertained. Electrophoretic mobility shift assay carried out with nuclear extract of Porteresia coarctata leaves grown under both control and stressed condition shows binding of nuclear proteins with the upstream elements. Nucleotide divergence among the different Oryza and Porteresia INO1 genes were calculated and compared.
机译:已通过纯化和免疫交叉反应的基质辅助激光解吸飞行时间质谱分析鉴定了稻米叶绿体1-肌-肌醇-1-磷酸合酶(MIPS; EC 5.5.1.4)的编码基因〜二维聚丙烯酰胺凝胶电泳后显示60 kDa的叶绿体蛋白,与OsINO1-1基因编码的胞质MIPS具有序列同一性。根据水稻基因组分析,在OsINO1-1基因上游发现了可能的叶绿体转运肽序列。 RT-PCR和共聚焦显微镜研究证实了转录,有效翻译及其作为叶绿体转运肽的功能。生物信息学分析在3号染色体上定位了叶绿体MIPS(OsINO1-1)基因,在10号染色体上定位了第二个MIPS基因(OsINO1-2),该基因缺少OsINO1-1中常规的叶绿体转运肽序列。鉴定并克隆了两个具有特征性启动子活性和上游顺式元件的新的PcINO1基因,但这些蛋白是否可以转移到叶绿体上尚待确定。用在控制和胁迫条件下生长的Porteresia coarctata叶片的核提取物进行的电泳迁移率迁移分析表明,核蛋白与上游元件结合。计算和比较了不同的稻和Porteresia INO1基因之间的核苷酸差异。

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