DIFFERENTIAL EXPRESSION OF CYTOCHROME-OXIDASE (COX) GENES IN DIFFERENT REGIONS OF MONKEY BRAIN

被引:34
作者
CHANDRASEKARAN, K
STOLL, J
GIORDANO, T
ATACK, JR
MATOCHA, MF
BRADY, DR
RAPOPORT, SI
机构
[1] Laboratory of Neurosciences, National Institute on Aging, National Institutes of Health, Bethesda, Maryland
[2] Abbott Laboratories, Dept 47-w AP-10, Abbott Park, Illinois
[3] Merck Sharp & Dohme Research Laboratories, Harlow, Essex
[4] Aids Research and Reference Reagent, Rockville, Maryland
关键词
FRONTAL CORTEX; CDNA LIBRARY; CYTOCHROME OXIDASE; SYNAPSES; DENDRITES; OXIDATIVE METABOLISM;
D O I
10.1002/jnr.490320313
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A frontal pole cDNA library from monkey (Macaca mulatta) brain was screened to identify mRNAs that are expressed more in frontal pole as compared to primary visual cortex. Three cDNA clones, whose greater expression was confirmed by Northern blot analysis, were identified as cytochrome oxidase (COX) subunits I, II, and III (COX I, II, and III). Each clone showed higher levels of mRNA in the frontal pole, dorsal lateral prefrontal cortex, and hippocampus than in the primary visual or somatosensory cortices. COX histochemistry of prefrontal, visual, and somatosensory cortical regions demonstrated heterogeneous distributions, with highest activity in dendrite-rich neuropil of the cortex. A laminar distribution of COX mRNA expression also was demonstrated with in situ hybridization. mRNA was detected in cell bodies and in apical dendrites. These results indicate region specific differences in the distribution of COX activity and in the corresponding mRNA for three of its subunits within the monkey brain. Such differences may be related to differences in the distribution of neuropil as compared with cell bodies among the brain regions studied, and may be relevant to selective vulnerability in Alzheimer's disease.
引用
收藏
页码:415 / 423
页数:9
相关论文
共 43 条
[1]   COMPLEMENTARY-DNA SEQUENCING - EXPRESSED SEQUENCE TAGS AND HUMAN GENOME PROJECT [J].
ADAMS, MD ;
KELLEY, JM ;
GOCAYNE, JD ;
DUBNICK, M ;
POLYMEROPOULOS, MH ;
XIAO, H ;
MERRIL, CR ;
WU, A ;
OLDE, B ;
MORENO, RF ;
KERLAVAGE, AR ;
MCCOMBIE, WR ;
VENTER, JC .
SCIENCE, 1991, 252 (5013) :1651-1656
[2]   SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
BANKIER, AT ;
BARRELL, BG ;
DEBRUIJN, MHL ;
COULSON, AR ;
DROUIN, J ;
EPERON, IC ;
NIERLICH, DP ;
ROE, BA ;
SANGER, F ;
SCHREIER, PH ;
SMITH, AJH ;
STADEN, R ;
YOUNG, IG .
NATURE, 1981, 290 (5806) :457-465
[3]   TOPOGRAPHY OF NEUROFIBRILLARY TANGLES AND GRANULOVACUOLES IN HIPPOCAMPI OF PATIENTS WITH DOWNS-SYNDROME - QUANTITATIVE COMPARISON WITH NORMAL AGING AND ALZHEIMERS-DISEASE [J].
BALL, MJ ;
NUTTALL, K .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1981, 7 (01) :13-20
[4]   PATTERNS OF CEREBRAL-CORTEX MESSENGER-RNA EXPRESSION [J].
BERNAL, J ;
GODBOUT, M ;
HASEL, KW ;
TRAVIS, GH ;
SUTCLIFFE, JG .
JOURNAL OF NEUROSCIENCE RESEARCH, 1990, 27 (02) :153-158
[5]   INDUCTION OF ALZHEIMER ANTIGENS BY AN UNCOUPLER OF OXIDATIVE-PHOSPHORYLATION [J].
BLASS, JP ;
BAKER, AC ;
KO, LW ;
BLACK, RS .
ARCHIVES OF NEUROLOGY, 1990, 47 (08) :864-869
[6]   METABOLIC ANATOMY OF BRAIN - A COMPARISON OF REGIONAL CAPILLARY DENSITY, GLUCOSE-METABOLISM, AND ENZYME-ACTIVITIES [J].
BOROWSKY, IW ;
COLLINS, RC .
JOURNAL OF COMPARATIVE NEUROLOGY, 1989, 288 (03) :401-413
[7]   HISTOCHEMICAL-CHANGES IN ENZYMES OF ENERGY-METABOLISM IN THE DENTATE GYRUS ACCOMPANY DEAFFERENTATION AND SYNAPTIC REORGANIZATION [J].
BOROWSKY, IW ;
COLLINS, RC .
NEUROSCIENCE, 1989, 33 (02) :253-262
[8]   STRUCTURE AND FUNCTION OF CYTOCHROME-C-OXIDASE [J].
CAPALDI, RA .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :569-596
[9]  
CARROLL EW, 1984, J COMP NEUROL, V222, P1, DOI 10.1002/cne.902220102
[10]  
CHANDRASEKARAN K, 1990, Society for Neuroscience Abstracts, V16, P344