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首页> 外文期刊>Phytochemistry >Isolation and characterization of cDNA clones encoding ADP-glucose pyrophosphorylase (AGPase) large and small subunits from chickpea (Cicer arietinum L.)
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Isolation and characterization of cDNA clones encoding ADP-glucose pyrophosphorylase (AGPase) large and small subunits from chickpea (Cicer arietinum L.)

机译:鹰嘴豆(Cicer arietinum L.)大,小亚基中编码ADP-葡萄糖焦磷酸化酶(AGPase)的cDNA克隆的分离和鉴定

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摘要

Four cDNA clones encoding two large subunits and two small subunits of the starch regulatory enzyme ADP-glucose pyrophosphorylase (AGPase) were isolated from a chickpea (Cicer arietinum L.) stem cDNA library. DNA sequence and Southern blot analyses of these clones, designated CagpL1, CagpL2 (large subunits) and CagpS1 and CagpS2 (small subunits), revealed that these isoforms represented different AGPase large and small subunits. RNA expression analysis indicated that CagpL1 was expressed strongly in leaves with reduced expression in the stem. No detectable expression was observed in seeds and roots. CagpL2 was expressed moderately in seeds followed by weak expression in leaves, stems and roots. Similar analysis showed that CagpS1 and CagPS2 displayed a spatial expression pattern similar to that observed for CagpL2 with the exception that CagpS1 showed a much higher expression in seeds than CagpS2. The spatial expression patterns of these different AGPase subunit sequences indicate that different AGPase isoforms are used to control starch biosynthesis in different organs during chickpea development.
机译:从鹰嘴豆(Cicer arietinum L.)茎cDNA文库中分离出编码淀粉调节酶ADP-葡萄糖焦磷酸化酶(AGPase)的两个大亚基和两个小亚基的四个cDNA克隆。这些克隆的DNA序列和Southern印迹分析分别命名为CagpL1,CagpL2(大亚基)和CagpS1和CagpS2(小亚基),发现这些亚型代表了不同的AGPase大亚基和小亚基。 RNA表达分析表明,CagpL1在叶片中强烈表达,在茎中表达减少。在种子和根中未观察到可检测的表达。 CagpL2在种子中中等表达,然后在叶,茎和根中弱表达。相似的分析表明,CagpS1和CagPS2的空间表达模式与CagpL2相似,不同的是,CagpS1在种子中的表达比CagpS2高得多。这些不同的AGPase亚基序列的空间表达模式表明,鹰嘴豆发育过程中,不同的AGPase亚型被用来控制淀粉在不同器官中的生物合成。

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