Posttranscriptional regulation of ATA2 transport during liver regeneration

被引:9
作者
Freeman, TL
Mailliard, ME
机构
[1] Univ Nebraska, Med Ctr, Dept Internal Med, Omaha, NE 68182 USA
[2] Vet Adm Med Ctr, Alcohol Study Unit, Omaha, NE 68105 USA
关键词
partial hepatectomy; System A; ATA2; SA1; liver regeneration; amino acid transport;
D O I
10.1006/bbrc.2000.3876
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
The recent cloning of ATA2, a cDNA displaying characteristics identical to the System A transporter, has provided the first molecular tool for study of System A-mediated amino acid transport in liver. Despite the 233 +/- 9 and 472 +/- 11% increase in System A transport activity following partial hepatectomy at 6 and 12 h, respectively, the steady-state level of ATA2 mRNA did not show a corresponding marked increase. Examination of the kinetic properties of System A following partial hepatectomy revealed a K-m of 0.26 +/- 0.04 mM which is consistent with the reported K-m for ATA2. These results indicate that a System A transporter present in regenerating liver and ATA2 are identical, but that the increase in System A activity following partial hepatectomy does not result from an increase in steady-state levels of ATA2 mRNA. These observations suggest that ATA2-mediated transport of amino acids is regulated at the posttranscriptional level. (C) 2000 Academic Press.
引用
收藏
页码:729 / 732
页数:4
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