Starvation-induced posttranscriptional control of rat liver mitochondrial citrate carrier expression

被引:23
作者
Siculella, L
Sabetta, S
di Summa, R
Leo, M
Giudetti, AM
Palmieri, F
Gnoni, GV
机构
[1] Univ Lecce, Dipartimento Sci & Tecnol Biol & Ambientali, Biochim Lab, I-73100 Lecce, Italy
[2] Univ Bari, Dipartimento Farmacobiol, Lab Biochim & Biol Mol, I-70125 Bari, Italy
关键词
starvation; refeeding; run-on assay; turnover; citrate carrier; mitochondrion; liver; rat;
D O I
10.1016/S0006-291X(02)02666-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Starvation has been associated with a reduced citrate carrier (CTP) activity in rat liver mitochondria. In the present study the molecular mechanism responsible for this reduction was investigated. Northern blot analysis performed with hepatic total RNA showed a decrease of about 40% in the CTP mRNA abundance in starved rats, when compared to fed animals. Nuclear run-on assay did not reveal any appreciable difference in the rate of CTP mRNA synthesis between the two groups of animals, while the apparent half-life of CTP mRNA in hepatocytes from fed and starved rats was 11 and 6 h, respectively. Therefore, these results suggest that in starved rats the regulation of hepatic CTP expression occurs at posttranscriptional level. Moreover, the reduced CTP activity in starved animals gradually increased by refeeding. The carrier activity reached fed rat values 6-9 h following refeeding. Interestingly, the accumulation of CTP mRNA raised in parallel with the transport activity. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:418 / 423
页数:6
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