The human cystathionine β-synthase (CBS) gene:: Complete sequence, alternative splicing, and polymorphisms

被引:99
作者
Kraus, JP
Oliveriusová, J
Sokolová, J
Kraus, E
Vlcek, C
de Franchis, R
Maclean, KN
Bao, LM
Bukovská, G
Patterson, D
Paces, V
Ansorge, W
Kozich, V
机构
[1] Univ Colorado, Sch Med, Dept Pediat, Denver, CO 80262 USA
[2] Charles Univ Prague, Fac Med 1, Inst Inherited Metab Disorders, Prague, Czech Republic
[3] Acad Sci Czech Republ, Inst Mol Genet, Prague, Czech Republic
[4] Eleanor Roosevelt Inst Canc Res, Denver, CO 80206 USA
[5] European Mol Biol Lab, Heidelberg, Germany
关键词
D O I
10.1006/geno.1998.5437
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cystathionine P-synthase [CBS; L-serine hydro-lyase (adding homocysteine), EC 4.2.1.22] catalyzes the first committed step of transsulfuration and is the enzyme deficient in classical homocystinuria, In this report, we describe the molecular cloning and the complete nucleotide sequence of the human CBS gene. We report a total of 28,046 nucleotides of sequence, which, in addition to the CBS gene, contains similar to 5 kb of the 5' flanking region. The human CBS gene contains 23 exons ranging from 42 to 209 bp. The 5' UTR is formed by 1 of 5 alternatively used exons and 1 invariably present exon, while the 3' UTR is encoded by exons 16 and 17. We also describe the identification of two alternatively used promoter regions that are GC rich (similar to 80%) and contain numerous putative binding sites for Sp1, Ap1, Ap2, and c-myb, but lack the classical TATA box. The CBS locus contains an unusually high number of Alu repeats, which may predispose this gene to deleterious rearrangements. Additionally, we report on a number of DNA sequence repeats that are polymorphic in North American and European Caucasians, (C) 1998 Academic Press.
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页码:312 / 324
页数:13
相关论文
共 55 条
[11]  
CLARKE R, 1991, NEW ENGL J MED, V325, P967
[12]   IDENTICAL GENOTYPES IN SIBLINGS WITH DIFFERENT HOMOCYSTINURIC PHENOTYPES - IDENTIFICATION OF 3 MUTATIONS IN CYSTATHIONINE BETA-SYNTHASE USING AN IMPROVED BACTERIAL EXPRESSION SYSTEM [J].
DEFRANCHIS, R ;
KOZICH, V ;
MCINNES, RR ;
KRAUS, JP .
HUMAN MOLECULAR GENETICS, 1994, 3 (07) :1103-1108
[13]   HOMOCYSTINURIA - HETEROZYGOTE DETECTION USING PHYTOHEMAGGLUTININ-STIMULATED LYMPHOCYTES [J].
GOLDSTEIN, JL ;
CAMPBELL, BK ;
GARTLER, SM .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (01) :218-221
[14]  
GOSS SJ, 1984, J CELL SCI, V68, P305
[15]  
GRIFFITH OW, 1987, METHOD ENZYMOL, V143, P366
[16]   Transfecting mammalian cells: Optimization of critical parameters affecting calcium-phosphate precipitate formation [J].
Jordan, M ;
Schallhorn, A ;
Wurm, FM .
NUCLEIC ACIDS RESEARCH, 1996, 24 (04) :596-601
[17]   Censor - A program for identification and elimination of repetitive elements from DNA sequences [J].
Jurka, J ;
Klonowski, P ;
Dagman, V ;
Pelton, P .
COMPUTERS & CHEMISTRY, 1996, 20 (01) :119-121
[18]  
Kaufman PB, 1995, HDB MOL CELLULAR MET
[19]  
Kery V, 1998, FASEB J, V12, pA1361
[20]   Trypsin cleavage of human cystathionine β-synthase into an evolutionarily conserved active core:: Structural and functional consequences [J].
Kery, V ;
Poneleit, L ;
Kraus, JP .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 355 (02) :222-232