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原位杂交显示磷酸烯醇丙酮酸羧激酶mRNA在大鼠肝实质门周区的主要定位。

Predominant localization of phosphoenolpyruvate carboxykinase mRNA in the periportal zone of rat liver parenchyma demonstrated by in situ hybridization.

作者信息

Bartels H, Linnemann H, Jungermann K

机构信息

Institut für Biochemie, Georg-August-Universität, Göttingen, FRG.

出版信息

FEBS Lett. 1989 May 8;248(1-2):188-94. doi: 10.1016/0014-5793(89)80459-4.

Abstract

In rat liver parenchyma, expression of the phosphoenolpyruvate carboxykinase (PEPCK) gene was studied by Northern blot analysis with a biotinylated cRNA probe and the zonal localization of PEPCK mRNA was demonstrated by in situ hybridization with a radiolabelled cRNA probe. During the feeding period at night, overall PEPCK mRNA levels were low and PEPCK mRNA was detected only in small areas of the periportal zone. At the beginning of the light period (7 am) the overall PEPCK mRNA level began increasing and the periportal areas containing PEPCK mRNA broadened. The maximum of the total abundance and of the area with high levels of PEPCK mRNA was reached at noon. Fasting for 24-72 h did not cause further significant alterations in the level or localization of PEPCK mRNA. The present data are in line with previous findings of the predominant localization of PEPCK activity and enzyme protein in periportal hepatocytes. They suggest that the heterogeneous expression of the PEPCK gene in rat liver is regulated at the pretranslational level.

摘要

在大鼠肝实质中,用生物素化的cRNA探针通过Northern印迹分析研究磷酸烯醇丙酮酸羧激酶(PEPCK)基因的表达,并用放射性标记的cRNA探针通过原位杂交证明PEPCK mRNA的区域定位。在夜间进食期间,PEPCK mRNA的总体水平较低,仅在门静脉周围区的小区域检测到PEPCK mRNA。在光照期开始时(上午7点),PEPCK mRNA的总体水平开始升高,含有PEPCK mRNA的门静脉周围区域变宽。中午时,PEPCK mRNA的总丰度和高水平区域达到最大值。禁食24 - 72小时未导致PEPCK mRNA水平或定位进一步发生显著变化。目前的数据与先前关于PEPCK活性和酶蛋白主要定位于门静脉周围肝细胞的研究结果一致。它们表明大鼠肝脏中PEPCK基因的异质性表达在翻译前水平受到调控。

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