MITOCHONDRIAL-GENOME-ENCODED RNAS - DIFFERENTIAL REGULATION BY CORTICOTROPIN IN BOVINE ADRENOCORTICAL-CELLS

被引:31
作者
RAIKHINSTEIN, M
HANUKOGLU, I
机构
[1] Department of Hormone Research, Weizmann Institute of Science
关键词
CYTOCHROME OXIDASE; NADH DEHYDROGENASE; ATPASE; STEROIDOGENESIS;
D O I
10.1073/pnas.90.22.10509
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Differential screening of an adrenal cortex cDNA library for corticotropin (ACTH)-inducible genes led to the isolation of a group of cDNAs representing mitochondrial genes that encode subunits of cytochrome oxidase, ATPase, and NADH dehydrogenase. Northern blot analysis of RNA from cells stimulated by ACTH confirmed the induction of these genes by ACTH yet revealed major differences in the relative responses of the respective mRNAs. The levels of mRNAs for cytochrome oxidase subunit I and ATPase increased 2- to 4-fold and for NADH dehydrogenase subunit 3 increased 20-fold, whereas the levels of the mitochondrial 16S rRNA showed no change within 6 h of ACTH stimulation. These effects of ACTH on mitochondrial mRNA levels probably result from both activation of the H2 transcription unit that encodes mitochondrial mRNAs and alteration of mRNA stability. ACTH also increased the activity of cytochrome oxidase after 12 h of stimulation. Examination of the tissue specificity of expression of five mitochondrial genes showed a wide range of RNA levels among 11 tissues but high correlations between individual RNA levels, consistent with a coordinated expression of the mitochondrial genes, although at different levels in each cell type. Proportionately high levels of mitochondrial mRNAs were found in adrenal cortex, probably reflecting a stimulatory effect of ACTH in vivo. Overall, the results indicate that ACTH enhances the energy-producing capacity of adrenocortical cells.
引用
收藏
页码:10509 / 10513
页数:5
相关论文
共 38 条
[1]   COMPLETE SEQUENCE OF BOVINE MITOCHONDRIAL-DNA - CONSERVED FEATURES OF THE MAMMALIAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
DEBRUIJN, MHL ;
COULSON, AR ;
EPERON, IC ;
SANGER, F ;
YOUNG, IG .
JOURNAL OF MOLECULAR BIOLOGY, 1982, 156 (04) :683-717
[2]   BIOGENESIS OF MITOCHONDRIA [J].
ATTARDI, G ;
SCHATZ, G .
ANNUAL REVIEW OF CELL BIOLOGY, 1988, 4 :289-333
[3]   REGULATION OF MITOCHONDRIAL GENE-EXPRESSION IN MAMMALIAN-CELLS [J].
ATTARDI, G ;
CHOMYN, A ;
KING, MP ;
KRUSE, B ;
POLOSA, PL ;
MURDTER, NN .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1990, 18 (04) :509-513
[4]   ESTROGEN INDUCTION OF CYTOCHROME-C-OXIDASE SUBUNIT-III IN RAT HIPPOCAMPUS [J].
BETTINI, E ;
MAGGI, A .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (05) :1923-1929
[5]   OPTIMAL CONDITIONS FOR DIRECTLY SEQUENCING DOUBLE-STRANDED PCR PRODUCTS WITH SEQUENASE [J].
CASANOVA, JL ;
PANNETIER, C ;
JAULIN, C ;
KOURILSKY, P .
NUCLEIC ACIDS RESEARCH, 1990, 18 (13) :4028-4028
[6]   CHANGES IN MITOCHONDRIAL AND MICROSOMAL 3-BETA-HYDROXYSTEROID DEHYDROGENASE-ACTIVITY IN MOUSE OVARY OVER THE COURSE OF THE ESTROUS-CYCLE [J].
CHAPMAN, JC ;
WATERHOUSE, TB ;
MICHAEL, SD .
BIOLOGY OF REPRODUCTION, 1992, 47 (06) :992-997
[7]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[8]   DIFFERENTIAL EXPRESSION OF THE MOUSE MITOCHONDRIAL GENES AND THE MITOCHONDRIAL RNA-PROCESSING ENDORIBONUCLEASE RNA BY ANDROGENS [J].
CORNWALL, GA ;
ORGEBINCRIST, MC ;
HANN, SR .
MOLECULAR ENDOCRINOLOGY, 1992, 6 (07) :1032-1042
[9]   ACTH INVIVO STIMULATION OF THE SYNTHESIS OF A SPECIFIC MITOCHONDRIAL PROTEIN IN THE RAT [J].
DAZORD, A ;
DESANTERRE, DG ;
SAEZ, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1981, 98 (04) :885-891
[10]  
DORFMAN DM, 1989, BIOTECHNIQUES, V7, P568