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肝脏再生过程中6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶的转录和转录后调控

Transcriptional and posttranscriptional regulation of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase during liver regeneration.

作者信息

Rosa J L, Tauler A, Lange A J, Pilkis S J, Bartrons R

机构信息

Departament de Ciències Fisiològiques Humanes i de la Nutrició, Universitat de Barcelona, Spain.

出版信息

Proc Natl Acad Sci U S A. 1992 May 1;89(9):3746-50. doi: 10.1073/pnas.89.9.3746.

Abstract

The control of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFK-2/FBPase-2; EC 2.7.1.105/3.1.3.46) gene expression during liver regeneration was studied. The level of PFK-2/FBPase-2 mRNA decreased to about 5% of the control value 6 hr after partial hepatectomy. Thereafter the mRNA increased to a maximum at 48 hr and returned to normal levels by 96 hr. In sham-operated animals, only a small increase was observed during the first 4 hr. The mRNA was recognized by a 299-base-pair liver-specific cDNA probe but not by a muscle-specific probe. The time course of mRNA modulation was well correlated with PFK-2/FBPase-2 activity and with the amount of bifunctional enzyme protein determined by immunoblotting with an antibody raised against the N-terminal decapeptide of liver PFK-2/FBPase-2. No alteration in the degradation rate of PFK-2/FBPase-2 mRNA was noted after partial hepatectomy. The modulation of PFK-2/FBPase-2 gene expression during liver regeneration involved changes in the transcription rate. The rate decreased by 50% at 6 hr after liver resection. The rate increased thereafter to a maximum at 72 hr and then returned to control values by 96 hr. The transcription rate of albumin did not change, whereas that of phosphoenolpyruvate carboxykinase increased 12-fold at 6 hr. These results show that PFK-2/FBPase-2 gene transcription is specifically regulated and that this regulation is in part responsible for the alterations in hepatic metabolism seen in regenerating liver.

摘要

研究了肝再生过程中6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶(PFK-2/FBPase-2;EC 2.7.1.105/3.1.3.46)基因表达的调控。部分肝切除术后6小时,PFK-2/FBPase-2 mRNA水平降至对照值的约5%。此后,mRNA在48小时达到最大值,并在96小时恢复到正常水平。在假手术动物中,最初4小时仅观察到少量增加。该mRNA可被一个299个碱基对的肝脏特异性cDNA探针识别,但不能被肌肉特异性探针识别。mRNA调节的时间进程与PFK-2/FBPase-2活性以及用针对肝脏PFK-2/FBPase-2 N端十肽产生的抗体通过免疫印迹法测定的双功能酶蛋白量密切相关。部分肝切除术后未发现PFK-2/FBPase-2 mRNA降解速率有改变。肝再生过程中PFK-2/FBPase-2基因表达的调节涉及转录速率的变化。肝切除术后6小时,转录速率下降50%。此后,转录速率在72小时达到最大值,然后在96小时恢复到对照值。白蛋白的转录速率没有变化,而磷酸烯醇式丙酮酸羧激酶的转录速率在6小时增加了12倍。这些结果表明,PFK-2/FBPase-2基因转录受到特异性调控,且这种调控部分负责再生肝脏中所见的肝脏代谢改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78f4/525567/e51af73028cd/pnas01083-0088-a.jpg

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