USE OF AVIDIN-BIOTIN SUBTRACTIVE HYBRIDIZATION TO CHARACTERIZE MESSENGER-RNA COMMON TO NEURONS DESTROYED BY THE SELECTIVE NEUROTOXICANT TRIMETHYLTIN

被引:28
作者
KRADY, JK
OYLER, GA
BALABAN, CD
BILLINGSLEY, ML
机构
[1] PENN STATE UNIV,MILTON S HERSHEY MED CTR,COLL MED,DEPT PHARMACOL,POB 850,HERSHEY,PA 17033
[2] PENN STATE UNIV,MILTON S HERSHEY MED CTR,COLL MED,CTR CELL & MOLEC BIOL,HERSHEY,PA 17033
[3] UNIV PITTSBURGH,SCH MED,INST EYE & EAR,DEPT OTOLARYNGOL,PITTSBURGH,PA 15213
来源
MOLECULAR BRAIN RESEARCH | 1990年 / 7卷 / 04期
关键词
cDNA; In situ hybridization; Neurotoxicology; Northern blot; Subtractive hybridization;
D O I
10.1016/0169-328X(90)90079-S
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Trimethyltin (TMT), a selective neurotoxicant, destroys a distinct subpopulation of neurons which possess no known biochemical or anatomic linkage. However, TMT-sensitive neurons may share common gene products related to susceptibility. In an effort to isolate mRNAs common to TMT-sensitive neurons, avidin/biotin based-subtractive hybridization was used to generate a cDNA library specifically related to TMT-toxicity. Out of 50 cDNAs, two clones hybridized only to poly(A+) mRNA isolated from the brains of saline-treated rats. Two of these cDNAs, p9T10 and p9T19, were used for in situ hybridization; both hybridized to hippocampus, limbic cortex, amygdala and other regions destroyed by TMT, suggesting that these probes identified mRNA enriched in TMT-sensitive neurons. The patterns of in situ hybridization coupled with the loss of p9T10 and p9T19 hybridization to mRNA isolated from the brains of TMT-treated rats suggests that one or both of these two clones may represent mRNA found in neurons damaged by TMT. The combination of selective neurotoxic lesions followed by cDNA subtractive hybridization should prove to be a useful strategy for the isolation of gene products from specific neuronal populations. © 1990.
引用
收藏
页码:287 / 297
页数:11
相关论文
共 33 条
[1]   THE NEURONAL MINERALOCORTICOID RECEPTOR AS A MEDIATOR OF GLUCOCORTICOID RESPONSE [J].
ARRIZA, JL ;
SIMERLY, RB ;
SWANSON, LW ;
EVANS, RM .
NEURON, 1988, 1 (09) :887-900
[3]   TRIMETHYLTIN-INDUCED NEURONAL DAMAGE IN THE RAT-BRAIN - COMPARATIVE STUDIES USING SILVER DEGENERATION STAINS, IMMUNOCYTOCHEMISTRY AND IMMUNOASSAY FOR NEURONOTYPIC AND GLIOTYPIC PROTEINS [J].
BALABAN, CD ;
OCALLAGHAN, JP ;
BILLINGSLEY, ML .
NEUROSCIENCE, 1988, 26 (01) :337-361
[4]   COMPLEXITY AND CHARACTERIZATION OF POLYADENYLATED RNA IN MOUSE-BRAIN [J].
BANTLE, JA ;
HAHN, WE .
CELL, 1976, 8 (01) :139-150
[5]   PATTERNS OF GENE-EXPRESSION IN THE MURINE BRAIN REVEALED BY INSITU HYBRIDIZATION OF BRAIN-SPECIFIC MESSENGER-RNAS [J].
BRANKS, PL ;
WILSON, MC .
MOLECULAR BRAIN RESEARCH, 1986, 1 (01) :1-16
[6]  
BROCK TO, 1987, J NEUROSCI, V7, P931
[7]  
BROWN AW, 1979, AM J PATHOL, V97, P59
[8]  
CHANDAI N, 1983, SCIENCE, V220, P924
[9]   COMPLEXITY OF CYTOPLASMIC POLYADENYLATED AND NONPOLYADENYLATED RAT-BRAIN RIBONUCLEIC-ACIDS [J].
CHIKARAISHI, DM .
BIOCHEMISTRY, 1979, 18 (15) :3249-3256
[10]   SEQUENCE COMPLEXITY OF NUCLEAR RNAS IN ADULT RAT TISSUES [J].
CHIKARAISHI, DM ;
DEEB, SS ;
SUEOKA, N .
CELL, 1978, 13 (01) :111-120