Analysis of the mouse selenoprotein P gene

被引:37
作者
Steinert, P [1 ]
Bächner, D [1 ]
Flohé, L [1 ]
机构
[1] Tech Univ Braunschweig, Dept Physiol Chem, D-38124 Braunschweig, Germany
关键词
BRN-2; GATA-1; genomic DNA; HNF3; in situ hybridization; selenoprotein P; SRY;
D O I
10.1515/bchm.1998.379.6.683
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
vertebrates several proteins containing a covalently bound selenocysteine residue have been identified. Among these, selenoprotein P is the most unusual one: depending on the species, 8-12 selenocysteine residues are cotranslationally integrated into the polypeptide chain. The protein was traced in rat plasma, but its role has not been worked out so far. In order to improve our understanding on selenoprotein P we investigated its tissue-specific expression and its genomic DNA. RNA in situ hybridization analyses confirmed the liver-specific expression in mice. Selenoprotein P was also found to be expressed in testis, brain, gut, and hemato cells. The murine selp gene contains five exons within 10.3 kb with a coding sequence restricted td exons 2 to 5. The complete gene including the selp promoter was sequenced. One TATA motif 38 bp upstream to exon 1 suggests transcription of selp by RNA, polymerase II. Within the 1116 bp upstream of exon 1 four hepatic nuclear factor 3 beta (HNF3 beta) binding motifs were found, which is in line with liver-specific expression of selenoprotein P.The expression in hematopoietic cells might be due to multiple GATA-1 motifs. Two BRN-2 motifs suitable for the binding of brain-specific regulatory factors correlated to the selenoprotein P:expression in the cerebellum. selenoprotein P was also expressed in Leydig cells which could be regulated by binding proteins docking to the SRY motifs present in the promoter region.
引用
收藏
页码:683 / 691
页数:9
相关论文
共 50 条
[1]  
AHRENS M, 1995, THESIS TU BRAUNSCHWE
[2]   MODEL OF FOREBRAIN REGIONALIZATION BASED ON SPATIOTEMPORAL PATTERNS OF POU-III HOMEOBOX GENE-EXPRESSION, BIRTH-DATES, AND MORPHOLOGICAL FEATURES [J].
ALVAREZBOLADO, G ;
ROSENFELD, MG ;
SWANSON, LW .
JOURNAL OF COMPARATIVE NEUROLOGY, 1995, 355 (02) :237-295
[3]   FORMATE DEHYDROGENASE OF CLOSTRIDIUM-THERMOACETICUM - INCORPORATION OF SELENIUM-75, AND EFFECTS OF SELENITE, MOLYBDATE, AND TUNGSTATE ON ENZYME [J].
ANDREESE.JR ;
LJUNGDAH.LG .
JOURNAL OF BACTERIOLOGY, 1973, 116 (02) :867-873
[4]  
[Anonymous], SCANDINAVIAN J RHEUM, DOI DOI 10.3109/03009749409117126
[5]   ENHANCED EXPRESSION OF THE MURINE FMR1 GENE DURING GERM-CELL PROLIFERATION SUGGESTS A SPECIAL FUNCTION IN BOTH THE MALE AND THE FEMALE GONAD [J].
BACHNER, D ;
MANCA, A ;
STEINBACH, P ;
WOHRLE, D ;
JUST, W ;
VOGEL, W ;
HAMEISTER, H ;
POUSTKA, A .
HUMAN MOLECULAR GENETICS, 1993, 2 (12) :2043-2050
[6]   IDENTIFICATION OF TYPE-I IODOTHYRONINE 5'-DEIODINASE AS A SELENOENZYME [J].
BEHNE, D ;
KYRIAKOPOULOS, A ;
MEINHOLD, H ;
KOHRLE, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (03) :1143-1149
[7]   RECOGNITION OF UGA AS A SELENOCYSTEINE CODON IN TYPE-I DEIODINASE REQUIRES SEQUENCES IN THE 3' UNTRANSLATED REGION [J].
BERRY, MJ ;
BANU, L ;
CHEN, Y ;
MANDEL, SJ ;
KIEFFER, JD ;
HARNEY, JW ;
LARSEN, PR .
NATURE, 1991, 353 (6341) :273-276
[8]   NEWER ROLES OF SELENIUM IN NUTRITION [J].
BURK, RF .
JOURNAL OF NUTRITION, 1989, 119 (07) :1051-1054
[9]   SELENOPROTEIN-P - A SELENIUM-RICH EXTRACELLULAR GLYCOPROTEIN [J].
BURK, RF ;
HILL, KE .
JOURNAL OF NUTRITION, 1994, 124 (10) :1891-1897
[10]  
CLARK LC, 1993, CANCER EPIDEM BIOMAR, V2, P41