THE RAT CENTRAL-NERVOUS-SYSTEM EXPRESSES ALZHEIMERS AMYLOID PRECURSOR PROTEIN APP(695), BUT NOT APP(677) (L-APP FORM)

被引:9
作者
OHGAMI, T
KITAMOTO, T
TATEISHI, J
机构
[1] KYUSHU UNIV 60,INST NEUROL,DEPT NEUROPATHOL,3-1-1 MAIDASHI,HIGASHI KU,FUKUOKA 812,JAPAN
[2] KYOWA BIORES LABS CO LTD,FUKUOKA,JAPAN
关键词
ALZHEIMERS DISEASE; BETA-A4 AMYLOID PRECURSOR PROTEIN; BETA-A4; PROTEIN; GENE EXPRESSION; ALTERNATIVE SPLICING; LEUKOCYTE-DERIVED BETA-A4 AMYLOID PRECURSOR PROTEIN;
D O I
10.1111/j.1471-4159.1993.tb13655.x
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
A novel splicing form of betaA4 amyloid precursor protein (APP) lacking exon 15, corresponding to 18 residues, was first reported in leukocytes and then in ubiquitous organs. To determine which APP molecules (APP695, APP751, or APP770) either with (N-APP) or without (L-APP; leukocyte-derived APP) exon 15 were expressed in various organs, we investigated the alternative splicing at exon 15 in the rat brain, kidney, heart, and testis by a PCR analysis of reverse-transcribed RNA and Southern blot analysis. Regarding APP695 without exons 7 and 8, L-APP was either seldom or never expressed in the brain, whereas both N- and L-APP were expressed in other organs. On the other hand, regarding APP751/770 containing exon 7, which codes for the Kunitz-type serine protease inhibitor domain, both N- and L-APP were expressed in all the organs examined, including the brain. These results suggest that a particular alternative regulation system related to exon 15 might be present in only APP695 of the brain and influence the proteolytic processing of APP.
引用
收藏
页码:1553 / 1556
页数:4
相关论文
共 20 条
[1]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[2]   EVIDENCE FOR LYSOSOMAL PROCESSING OF AMYLOID BETA-PROTEIN PRECURSOR IN CULTURED-CELLS [J].
COLE, GM ;
HUYNH, TV ;
SAITOH, T .
NEUROCHEMICAL RESEARCH, 1989, 14 (10) :933-939
[3]   CLEAVAGE OF AMYLOID-BETA PEPTIDE DURING CONSTITUTIVE PROCESSING OF ITS PRECURSOR [J].
ESCH, FS ;
KEIM, PS ;
BEATTIE, EC ;
BLACHER, RW ;
CULWELL, AR ;
OLTERSDORF, T ;
MCCLURE, D ;
WARD, PJ .
SCIENCE, 1990, 248 (4959) :1122-1124
[4]   POTENTIALLY AMYLOIDOGENIC, CARBOXYL-TERMINAL DERIVATIVES OF THE AMYLOID PROTEIN-PRECURSOR [J].
ESTUS, S ;
GOLDE, TE ;
KUNISHITA, T ;
BLADES, D ;
LOWERY, D ;
EISEN, M ;
USIAK, M ;
QU, XM ;
TABIRA, T ;
GREENBERG, BD ;
YOUNKIN, SG .
SCIENCE, 1992, 255 (5045) :726-728
[5]   ALZHEIMERS-DISEASE - INITIAL REPORT OF THE PURIFICATION AND CHARACTERIZATION OF A NOVEL CEREBROVASCULAR AMYLOID PROTEIN [J].
GLENNER, GG ;
WONG, CW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 120 (03) :885-890
[6]   PROCESSING OF THE AMYLOID PROTEIN-PRECURSOR TO POTENTIALLY AMYLOIDOGENIC DERIVATIVES [J].
GOLDE, TE ;
ESTUS, S ;
YOUNKIN, LH ;
SELKOE, DJ ;
YOUNKIN, SG .
SCIENCE, 1992, 255 (5045) :728-730
[7]   DIFFERENTIAL SPLICING OF ALZHEIMERS-DISEASE AMYLOID A4 PRECURSOR RNA IN RAT-TISSUES - PREA4695 MESSENGER-RNA IS PREDOMINANTLY PRODUCED IN RAT AND HUMAN BRAIN [J].
KANG, J ;
MULLERHILL, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 166 (03) :1192-1200
[8]   THE PRECURSOR OF ALZHEIMERS-DISEASE AMYLOID-A4 PROTEIN RESEMBLES A CELL-SURFACE RECEPTOR [J].
KANG, J ;
LEMAIRE, HG ;
UNTERBECK, A ;
SALBAUM, JM ;
MASTERS, CL ;
GRZESCHIK, KH ;
MULTHAUP, G ;
BEYREUTHER, K ;
MULLERHILL, B .
NATURE, 1987, 325 (6106) :733-736
[9]   THE SEQUENCE OF THE 2 EXTRA EXONS IN RAT PREA4 [J].
KANG, J ;
MULLERHILL, B .
NUCLEIC ACIDS RESEARCH, 1989, 17 (05) :2130-2130
[10]   NOVEL PRECURSOR OF ALZHEIMERS-DISEASE AMYLOID PROTEIN SHOWS PROTEASE INHIBITORY ACTIVITY [J].
KITAGUCHI, N ;
TAKAHASHI, Y ;
TOKUSHIMA, Y ;
SHIOJIRI, S ;
ITO, H .
NATURE, 1988, 331 (6156) :530-532