Mouse palmitoyl protein thioesterase: Gene structure and expression of cDNA

被引:11
作者
Salonen, T
Hellsten, E
Horelli-Kuitunen, N
Peltonen, L
Jalanko, A [1 ]
机构
[1] Univ Helsinki, Natl Publ Hlth Inst, FIN-00300 Helsinki, Finland
[2] Univ Helsinki, Inst Biomed, Dept Human Mol Genet, FIN-00300 Helsinki, Finland
[3] Univ Helsinki, Cent Hosp, Meilahti Hosp, Mol Genet Lab, FIN-00290 Helsinki, Finland
来源
GENOME RESEARCH | 1998年 / 8卷 / 07期
关键词
D O I
10.1101/gr.8.7.724
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
Palmitoyl protein thioesterase (PPT) is the defective enzyme in infantile neuronal ceroid lipofuscinosis (INCL), which is a recessively inherited, progressive neurodegenerative disorder. We present here the cloning, chromosomal mapping, genomic structure, and the expression of the cDNA of mouse PPT. The mouse PPT gene spans >21 kb of genomic DNA and contains nine exons with a coding sequence of 918 bp. Fluorescence in situ hybridization to metaphase chromosomes localized the mouse PPT gene to the chromosome 4 conserved syntenic region with human chromosome 1p32 where the human PPT is located. PPT is expressed widely in a variety of mouse tissues. The mouse PPT cDNA is conserved highly with the human and rat PPT both at the nucleotide and amino acid sequence level. Transient expression of mouse PP7 in COS-1 cells yielded a 38/36-kD differentially glycosylated polypeptide that was also secreted into culture media. Immunofluorescence analysis of transiently transfected HeLa cells indicated lysosomal localization of mouse PPT. Based on the high conservation of the gene and polypeptide structure as well as similar processing and intracellular localization, the function of PPT in mouse and human are likely to be very similar.
引用
收藏
页码:724 / 730
页数:7
相关论文
共 27 条
[11]   OVEREXPRESSION OF HUMAN ALPHA-GALACTOSIDASE-A RESULTS IN ITS INTRACELLULAR AGGREGATION, CRYSTALLIZATION IN LYSOSOMES, AND SELECTIVE SECRETION [J].
IOANNOU, YA ;
BISHOP, DF ;
DESNICK, RJ .
JOURNAL OF CELL BIOLOGY, 1992, 119 (05) :1137-1150
[12]   INFANTILE FORM OF NEURONAL CEROID LIPOFUSCINOSIS (CLN1) MAPS TO THE SHORT ARM OF CHROMOSOME-1 [J].
JARVELA, I ;
SCHLEUTKER, J ;
HAATAJA, L ;
SANTAVUORI, P ;
PUHAKKA, L ;
MANNINEN, T ;
PALOTIE, A ;
SANDKUIJL, LA ;
RENLUND, M ;
WHITE, R ;
AULA, P ;
PELTONEN, L .
GENOMICS, 1991, 9 (01) :170-173
[13]  
JARVELA I, 1997, IN PRESS
[14]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[15]  
PALMER DN, 1986, J BIOL CHEM, V261, P1773
[16]   CYTOPLASMIC INCLUSIONS IN VERMIFORM APPENDIX AND SKELETAL-MUSCLE IN 2 TYPES OF SO-CALLED NEURONAL CEROID-LIPOFUSCINOSIS [J].
RAPOLA, J ;
HALTIA, M .
BRAIN, 1973, 96 (DEC) :833-&
[17]  
Sambrook J., 2002, MOL CLONING LAB MANU
[18]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467
[19]  
SANTAVUORI P, 1974, DEV MED CHILD NEUROL, V16, P644
[20]   cDNA and genomic cloning of human palmitoyl-protein thioesterase (PPT), the enzyme defective in infantile neuronal ceroid lipofuscinosis [J].
Schriner, JE ;
Yi, W ;
Hofmann, SL .
GENOMICS, 1996, 34 (03) :317-322