EVIDENCE OF POSTTRANSCRIPTIONAL REGULATION IN MAMMALIAN MITOCHONDRIAL BIOGENESIS

被引:29
|
作者
IZQUIERDO, JM [1 ]
CUEZVA, JM [1 ]
机构
[1] UNIV AUTONOMA MADRID,CSIC,CTR BIOL MOLEC SEVERO OCHOA,DEPT BIOL MOLEC,E-28049 MADRID,SPAIN
关键词
D O I
10.1006/bbrc.1993.2215
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
We have previously shown that the nuclear-encoded gene’s expression of mitochondrial β-subunit of the F1-ATPase complex in rat liver is regulated at the translational level (Luis, A.M., Izquierdo, J.M., Ostronoff, L.K., Santaren, J., Salinas, M., and Cuezva, J.M. (1993) J. Biol. Chem. 268, 1868-1875). In this paper we report that the different steady-state levels of ATP synthase β subunit mRNA detected in rat tissues are not paralleled by a proportional content of immunodetectable β-F1-ATPase protein. The results suggest that tissue-specific transcriptional and post-transcriptional mechanisms contribute to differential mitochondrial biogenesis in mammalian cells. On the other hand, steady-state mRNA levels of the mitochondrial encoded ATP synthase subunits (ATP 6 + 8) indicate that nuclear and mitochondrial-encoded transcripts for this complex are in close relation, that is, the expression of both nuclear and mitochondrial genes is coordinated in all tissues examined. © 1993 Academic Press, Inc.
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页码:55 / 60
页数:6
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