Age-related expression analysis of mouse liver nuclear protein binding to 3'-untranslated region of Period2 gene

被引:0
作者
Hamada, Toshiyuki [1 ,2 ]
Miyakawa, Kazuko [3 ]
Kushige, Hiroko [4 ]
Shibata, Shigenobu [3 ]
Kurachi, Sumiko [5 ]
机构
[1] Hokkaido Univ, Appl Mol Imaging Phys, Grad Sch Med, Sapporo, Hokkaido 0608638, Japan
[2] Hakujikai Inst Gerontol, Adachi Ward, Tokyo 1230864, Japan
[3] Waseda Univ, Sch Adv Sci & Engn, Lab Physiol & Pharmacol, Shinjuku Ward, Tokyo 1628480, Japan
[4] Natl Inst Adv Ind Sci & Technol, AIST Tsukuba Ctr 6 13, Age Dimens Res Ctr, Tsukuba, Ibaraki 3058566, Japan
[5] Univ Washington, Div Med Genet, Dept Med, Seattle, WA 98195 USA
关键词
Period; 2; hnRNP; Circadian rhythm; Aging; Homeostasis; MESSENGER-RNA DEGRADATION; CIRCADIAN OSCILLATION; ARGININE METHYLATION; PROTEOMIC ANALYSIS; BLOOD-COAGULATION; FACTOR-IX; HNRNP A1; PHOSPHORYLATION; TRANSLATION; MAINTENANCE;
D O I
10.1007/s12576-015-0373-8
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
In mammals, both circadian rhythm and aging play important roles in regulating time-dependent homeostasis. We previously discovered an age-related increase element binding protein, hnRNP A3, which binds to the 3'-untranslated region (UTR) of blood coagulation factor IX (FIX). Here, we describe other members of this protein family, hnRNP C and hnRNP H, which bind to the 3'-UTR of the mouse circadian clock gene Period 2 (mPer2). RNA electrophoretic mobility shift assays using a P-32-labeled Per2 RNA probe coupled with two-dimensional gel electrophoresis followed by MALDI-TOF/MS peptide mass fingerprint analysis was used to analyze these proteins. Western blotting suggested that the total expression of these proteins in mouse liver cell nuclei does not increase with age. Two-dimensional gel electrophoresis analysis of age-related protein expression showed that many isoforms of these proteins exist in the liver and that each protein exhibits a complex age-related expression pattern. These results suggest that many isoforms of proteins are regulated by different aging systems and that many age regulation systems function in the liver.
引用
收藏
页码:349 / 357
页数:9
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