Singh Salvinder, Choi Sang-Bong, Modi Mahendra K, Okita Thomas W
Institute of Biological Chemistry, Washington State University, PO Box 646340, Pullman, WA 99164-6340, USA.
Phytochemistry. 2002 Feb;59(3):261-8. doi: 10.1016/s0031-9422(01)00457-5.
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.
从鹰嘴豆(Cicer arietinum L.)茎cDNA文库中分离出四个编码淀粉调节酶ADP-葡萄糖焦磷酸化酶(AGPase)两个大亚基和两个小亚基的cDNA克隆。对这些分别命名为CagpL1、CagpL2(大亚基)以及CagpS1和CagpS2(小亚基)的克隆进行DNA序列和Southern印迹分析,结果表明这些同工型代表不同的AGPase大亚基和小亚基。RNA表达分析表明,CagpL1在叶片中强烈表达,在茎中的表达降低。在种子和根中未观察到可检测到的表达。CagpL2在种子中适度表达,随后在叶、茎和根中弱表达。类似分析表明,CagpS1和CagpS2呈现出与CagpL2类似的空间表达模式,不同之处在于CagpS1在种子中的表达比CagpS2高得多。这些不同AGPase亚基序列的空间表达模式表明,在鹰嘴豆发育过程中,不同的AGPase同工型用于控制不同器官中的淀粉生物合成。