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The 6-phosphogluconate Dehydrogenase Genes Are Responsive to Abiotic Stresses in Rice 被引量:7
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作者 Fu-Yun Hou Ji Huang Shan-Lin Yu Hong-Sheng Zhang 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2007年第5期655-663,共9页
Glucose-6-phosphate dehydrogenase (G6PDH, E.C. 1.1.1.49) and 6-phosphogluconate dehydrogenase (6PGDH, EC 1.1.1.44) are both key enzymes of the pentose phosphate pathway (PPP). The OsG6PDH1 and Os6PGDH1 genes enc... Glucose-6-phosphate dehydrogenase (G6PDH, E.C. 1.1.1.49) and 6-phosphogluconate dehydrogenase (6PGDH, EC 1.1.1.44) are both key enzymes of the pentose phosphate pathway (PPP). The OsG6PDH1 and Os6PGDH1 genes encoding cytosolic G6PDH and cytosolic 6PGDH were Isolated from rice (Oryza sativa L.). We have shown that Os6PGDH1 gene was up-regulated by salt stress. Here we reported the isolation and characterization of Os6PGDH2 from rice, which encode the plastidic counterpart of 6PGDH. Genomic organization analysis indicated that OsG6PDH1 and OsG6PDH2 genes contain multiple introns, whereas two Os6PGDH1 and Os6PGDH2 genes have no introns in their translated regions. In a step towards understanding the functions of the pentose phosphate pathway in plants in response to various abiotic stresses, the expressions of four genes in the rice seedlings treated by drought, cold, high salinity and abscisic acid (ABA) were investigated. The results show that OsG6PDH1 and OsG6PDH2 are not markedly regulated by the abiotic stresses detected. However, the transcript levels of both Os6PGDH1 and Os6PGDH2 are up-regulated in rice seedlings under drought, cold, high salinity and ABA treatments. Meanwhile, the enzyme activities of G6PDH and 6PGDH in the rice seedlings treated by various abiotic stresses were Investigated. Like the mRNA expression patterns, G6PDH activity remains constant but the 6PGDH Increases steadily during the treatments. Taken together, we suggest that the pentose phosphate pathway may play an important role in rice responses to abiotic stresses and the second key enzyme of PPP, 6PGDH, may function as a regulator controlling the efficiency of the pathway under abiotic stresses. 展开更多
关键词 6-phosphogluconate dehydrogenase abiotic stresses glucose-6-phophate dehydrogenase Oryza sativa pentose phosphate pathway.
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二氢硫辛酰转乙酰基酶通过乙酰化磷酸葡糖酸脱氢酶促进核酸合成 被引量:2
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作者 孙明明 乔亚亚 +2 位作者 李垒垒 山长亮 张帅 《中国生物化学与分子生物学报》 CAS CSCD 北大核心 2021年第3期339-346,共8页
丙酮酸脱氢酶复合物(pyruvate dehydrogenase complex,PDC)是位于线粒体内的多酶复合物,催化丙酮酸不可逆地氧化脱羧转为乙酰辅酶A,二氢硫辛酰转乙酰基酶(dihydrolipoyl acetyltransferase,DLAT)是PDC的1个亚基。PDC在细胞线粒体呼吸中... 丙酮酸脱氢酶复合物(pyruvate dehydrogenase complex,PDC)是位于线粒体内的多酶复合物,催化丙酮酸不可逆地氧化脱羧转为乙酰辅酶A,二氢硫辛酰转乙酰基酶(dihydrolipoyl acetyltransferase,DLAT)是PDC的1个亚基。PDC在细胞线粒体呼吸中发挥关键作用。但是DLAT在核酸合成中的作用仍不清楚。在本研究中,首先利用GEO数据库、Oncomine数据库和人类蛋白质图谱数据库分析发现,DLAT在肺癌组织中的表达明显高于癌旁组织(P=0.0002),并且高表达DLAT的病人有较短的生存期(HR=1.47,logrank P=4e-09)。因此推测,DLAT在肿瘤生长中发挥关键作用。进而本文构建了敲低DLAT的肺癌细胞系,并用免疫印迹结果验证了DLAT敲低效果。进一步的研究发现,敲低DLAT将降低戊糖磷酸途径第3个酶磷酸葡糖酸脱氢酶(6-phosphogluconate dehydrogenase,6PGD)的乙酰化水平,进而降低6PGD酶活性,从而导致核酸合成受阻(P<0.01),最终抑制肺癌细胞增殖(P<0.01)。机制研究发现,DLAT通过乙酰化6PGD而使其酶活性增强,进而提高核酸合成,从而达到促进肺癌细胞增殖的作用。综上所述,本研究为DLAT作为潜在的靶点,为药物开发和临床肺癌的治疗提供了新的思路。 展开更多
关键词 线粒体 二氢硫辛酰转乙酰基酶 磷酸葡糖酸脱氢酶 戊糖磷酸途径
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