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锰缺乏小鼠肝脏及大鼠发育过程中锰对锰超氧化物歧化酶的转录调控。

Transcriptional regulation of MnSOD by manganese in the liver of manganese-deficient mice and during rat development.

作者信息

Borrello S, De Leo M E, Galeotti T

机构信息

Institute of General Pathology, Catholic University, Rome, Italy.

出版信息

Biochem Int. 1992 Dec;28(4):595-601.

PMID:1482398
Abstract

Evidence is reported that liver manganese deficiency, whether artificially produced by the administration of a Mn-deficient diet, or physiologically occurring in the neonatal life, in mice and rats respectively, causes the down-regulation of the manganese-containing superoxide dismutase at (pre)-transcriptional level. These observations, in addition to previous data concerning Mn-deficiency and the low level of expression of MnSOD in Morris hepatomas, strongly support the role played by the metal ion in the control of the MnSOD by a mechanism of gene activation. While the molecular events taking place in such regulation are not yet identified, the involvement of reactive oxygen species (ROS) as second messengers in the activation of specific transcription factors is suggested.

摘要

有证据表明,无论是通过给予缺锰饮食人工造成的肝脏锰缺乏,还是分别在新生小鼠和大鼠生理上出现的锰缺乏,都会在转录(前)水平导致含锰超氧化物歧化酶的下调。这些观察结果,除了之前关于锰缺乏和莫里斯肝癌中锰超氧化物歧化酶低表达水平的数据外,有力地支持了金属离子通过基因激活机制在控制锰超氧化物歧化酶中所起的作用。虽然尚未确定这种调节中发生的分子事件,但提示活性氧(ROS)作为第二信使参与特定转录因子的激活。

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