Effects of oxygen concentration on the expression of cytochrome c and cytochrome c oxidase genes in yeast

被引:109
作者
Burke, PV [1 ]
Raitt, DC [1 ]
Allen, LA [1 ]
Kellogg, EA [1 ]
Poyton, RO [1 ]
机构
[1] UNIV COLORADO, DEPT MOL CELLULAR & DEV BIOL, BOULDER, CO 80309 USA
关键词
D O I
10.1074/jbc.272.23.14705
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
Oxygen is an important environmental regulator for the transcription of several genes in Saccharomyces cerevisiae, but it is not yet clear how this yeast or other eukaryotes actually sense oxygen. To begin to address this we have examined the effects of oxygen concentration on the expression of several nuclear genes (CYC1, CYC7, COX4, COX5a, COX5b, COX6, COX7, COX8, and COX9) for proteins of the terminal portion of the respiratory chain. COX5b and CYC7 are hypoxic genes; the rest are aerobic genes. We have found that the level of expression of these genes is determined by oxygen concentration per se and not merely the presence or absence of oxygen and that each of these genes has a low oxygen threshold (0.5-1 mu M O-2) for expression. For some aerobic genes (COX4, COX5a, COX7, COX8, and COX9) there is a gradual decline in expression between 200 mu M O-2 (air) and their oxygen threshold. Below this threshold expression drops precipitously. For others (COX5a and CYC1) the level of expression is nearly constant between 200 mu M O-2 and their threshold and then drops off. The hypoxic genes COX5b and CYC7 are not expressed until the oxygen concentration is below 0.5 mu M O-2. These studies have also revealed that COX5a and CYC1, the genes for the aerobic isoforms of cytochrome c oxidase subunit V and cytochrome c, and COX5b and CYC7, the genes for the hypoxic isoforms of cytochrome c oxidase subunit V and cytochrome c, are coexpressed at a variety of oxygen concentrations and switch on or off at extremely low oxygen concentrations. By shifting cells from one oxygen concentration to another we have found that aerobic genes are induced faster than hypoxic genes and that transcripts from both types of gene are turned over quickly. These findings have important implications for cytochrome c oxidase function and biogenesis and far models of oxygen sensing in yeast.
引用
收藏
页码:14705 / 14712
页数:8
相关论文
共 41 条
[1]   ISOFORMS OF YEAST CYTOCHROME-C-OXIDASE SUBUNIT-V AFFECT THE BINUCLEAR REACTION-CENTER AND AFTER THE KINETICS OF INTERACTION WITH THE ISOFORMS OF YEAST CYTOCHROME-C [J].
ALLEN, LA ;
ZHAO, XJ ;
CAUGHEY, W ;
POYTON, RO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (01) :110-118
[2]  
[Anonymous], BIOSYNTHESIS HEME CO
[3]   Oxygen sensing and molecular adaptation to hypoxia [J].
Bunn, HF ;
Poyton, RO .
PHYSIOLOGICAL REVIEWS, 1996, 76 (03) :839-885
[4]   DESIGN OF A SYSTEM FOR THE CONTROL OF LOW DISSOLVED-OXYGEN CONCENTRATIONS - CRITICAL OXYGEN CONCENTRATIONS FOR AZOTOBACTER-VINELANDII AND ESCHERICHIA-COLI [J].
CHEN, J ;
TANNAHILL, AL ;
SHULER, ML .
BIOTECHNOLOGY AND BIOENGINEERING, 1985, 27 (02) :151-155
[5]   PROMITOCHONDRIA OF ANAEROBICALLY GROWN YEAST .I. ISOLATION AND BIOCHEMICAL PROPERTIES [J].
CRIDDLE, RS ;
SCHATZ, G .
BIOCHEMISTRY, 1969, 8 (01) :322-+
[6]   2 NONIDENTICAL FORMS OF SUBUNIT-V ARE FUNCTIONAL IN YEAST CYTOCHROME-C OXIDASE [J].
CUMSKY, MG ;
KO, C ;
TRUEBLOOD, CE ;
POYTON, RO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (08) :2235-2239
[7]   STRUCTURAL-ANALYSIS OF 2 GENES ENCODING DIVERGENT FORMS OF YEAST CYTOCHROME-C-OXIDASE SUBUNIT-V [J].
CUMSKY, MG ;
TRUEBLOOD, CE ;
KO, C ;
POYTON, RO .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (10) :3511-3519
[8]  
DECKERT J, 1995, GENETICS, V139, P1149
[9]   GLOBAL REGULATION OF MITOCHONDRIAL BIOGENESIS IN SACCHAROMYCES-CEREVISIAE [J].
DEWINDE, JH ;
GRIVELL, LA .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 46, 1993, 46 :51-91
[10]   RNA FROM THE YEAST TRANSPOSABLE ELEMENT TY1 HAS BOTH ENDS IN THE DIRECT REPEATS, A STRUCTURE SIMILAR TO RETROVIRUS RNA [J].
ELDER, RT ;
LOH, EY ;
DAVIS, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (09) :2432-2436