FROG DIAZEPAM-BINDING INHIBITOR - PEPTIDE SEQUENCE, CDNA CLONING, AND EXPRESSION IN THE BRAIN

被引:56
作者
LIHRMANN, I
PLAQUEVENT, JC
TOSTIVINT, H
RAIJMAKERS, R
TONON, MC
CONLON, JM
VAUDRY, H
机构
[1] UNIV ROUEN, EUROPEAN INST PEPTIDE RES, CELLULAR & MOLEC NEUROENDOCRINOL LAB,CNRS, INSERM, F-76821 MONT ST AIGNAN, FRANCE
[2] CREIGHTON UNIV, SCH MED, CTR REGULATORY PEPTIDE, DEPT BIOMED SCI, OMAHA, NE 68178 USA
关键词
BENZODIAZEPINE-RECEPTOR LIGANDS; PEPTIDE MICROSEQUENCING; NUCLEOTIDE SEQUENCE; GLIAL CELLS; EVOLUTION;
D O I
10.1073/pnas.91.15.6899
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
Three peptides derived from diazepam-binding inhibitor (DBI) were isolated in pure form from the brain of the frog Rana ridibunda. The primary structures of these peptides showed that they correspond to mammalian DBI-(1-39), DBI-(58-87), and DBI-(70-87). A set of degenerate primers, whose design was based on the amino acid sequence data, was used to screen a frog brain cDNA library. The cloned cDNA encodes an 87-amino acid polypeptide, which exhibits 68% similarity with porcine and bovine DBI. Frog DBI contains two paired basic amino acids (Lys-Lys) at positions 14-15 and 62-63 and a single cysteine within the biologically active region of the molecule. Northern blot analysis showed that DBI mRNA is expressed at a high level in the brain but is virtually absent in peripheral tissues. The distribution of DBI mRNA and DBI-like immunoreactivity in the frog brain was studied by in situ hybridization and immunocytochemistry. Both approaches revealed that the DBI gene is expressed in ependymal cells and circumventricular organs lining the ventricular cavity. Since amphibia diverged from mammals at least 250 million years ago, the data show that evolutionary pressure has acted to conserve the structure of DBI in the vertebrate phylum. The distribution of both DBI mRNA and DBI-like immunoreactivity indicates that DBI is selectively expressed in glial cells.
引用
收藏
页码:6899 / 6903
页数:5
相关论文
共 40 条
[11]   ISOLATION, CHARACTERIZATION, AND PURIFICATION TO HOMOGENEITY OF AN ENDOGENOUS POLYPEPTIDE WITH AGONISTIC ACTION ON BENZODIAZEPINE RECEPTORS [J].
GUIDOTTI, A ;
FORCHETTI, CM ;
CORDA, MG ;
KONKEL, D ;
BENNETT, CD ;
COSTA, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (11) :3531-3535
[12]   DETERMINATION BY PHOTOAFFINITY-LABELING OF THE HYDROPHOBIC PART OF THE BINDING-SITE FOR ACYL-COA ESTERS ON ACYL-COA-BINDING PROTEIN FROM BOVINE LIVER [J].
HACH, M ;
PEDERSEN, SN ;
BORCHERS, T ;
HOJRUP, P ;
KNUDSEN, J .
BIOCHEMICAL JOURNAL, 1990, 271 (01) :231-236
[13]   CHARACTERIZATION OF THE CDNA-ENCODING PROOPIOMELANOCORTIN IN THE FROG RANA-RIDIBUNDA [J].
HILARIO, E ;
LIHRMANN, I ;
VAUDRY, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (02) :653-659
[14]   AN OCTADECANEUROPEPTIDE (ODN) DERIVED FROM DIAZEPAM BINDING INHIBITOR INCREASES AGGRESSIVE INTERACTIONS IN MICE [J].
KAVALIERS, M ;
HIRST, M .
BRAIN RESEARCH, 1986, 383 (1-2) :343-349
[15]  
KETTENMANN H, 1988, GLIAL CELL RECEPTORS, P95
[16]   RAPID AND SENSITIVE PROTEIN SIMILARITY SEARCHES [J].
LIPMAN, DJ ;
PEARSON, WR .
SCIENCE, 1985, 227 (4693) :1435-1441
[17]  
LOUISET E, 1993, MELANOTROPIC PEPTIDE, V680, P564
[18]   ONTOGENY OF DIAZEPAM-BINDING INHIBITOR-RELATED PEPTIDES (ENDOZEPINES) IN THE RAT-BRAIN [J].
MALAGON, M ;
VAUDRY, H ;
VANSTRIEN, F ;
PELLETIER, G ;
GRACIANAVARRO, F ;
TONON, MC .
NEUROSCIENCE, 1993, 57 (03) :777-786
[19]   LOCALIZATION AND CHARACTERIZATION OF DIAZEPAM-BINDING INHIBITOR (DBI)-LIKE PEPTIDES IN THE BRAIN AND PITUITARY OF THE TROUT (SALMO-GAIRDNERI) [J].
MALAGON, M ;
VALLARINO, M ;
TONON, MC ;
VAUDRY, H .
BRAIN RESEARCH, 1992, 576 (02) :208-214
[20]   DISTRIBUTION AND CHARACTERIZATION OF ENDOZEPINE-LIKE IMMUNOREACTIVITY IN THE CENTRAL-NERVOUS-SYSTEM OF THE FROG RANA-RIDIBUNDA [J].
MALAGON, M ;
VAUDRY, H ;
VALLARINO, M ;
GRACIANAVARRO, F ;
TONON, MC .
PEPTIDES, 1992, 13 (01) :99-107