The number of kringle IV repeats 3-10 is invariable in the human apo(a) gene

被引:19
作者
Haibach, C [1 ]
Kraft, HG [1 ]
Köchl, S [1 ]
Abe, A [1 ]
Utermann, G [1 ]
机构
[1] Univ Innsbruck, Inst Med Biol & Human Genet, A-6020 Innsbruck, Austria
基金
奥地利科学基金会;
关键词
apolipoprotein(a); genomic DNA; YAC; restriction map; RFLP;
D O I
10.1016/S0378-1119(97)00657-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The human apolipoprotein(a) (apo(a)) gene is a member of a family of related genes including plasminogen, apo(a)rg-B and apo(a)rg-C, which are clustered on chromosome 6q 2,7. Apo(a) contains ten different types of plasminogen-like kringle IV repeats (K-IV 1-10) one of which (K-IV 2) varies in number resulting in a remarkable size polymorphism of the protein. Sequence analysis of human apo(a) alleles and indirect evidence have suggested that K-IV 1 and K-IV 3-10 are each present once in individual alleles and that the 3' apo(a) region encompassing kringles IV 3-10, kringle V and the protease domain is invariable. To directly test this, we have constructed a restriction map of the apo(a) gene region from genomic DNA and from a yeast artificial chromosome (YAC) (K-IV 13) which contain the entire apo(a) gene. The presence of a 63 kb ClaI fragment encompassing kringles IV 3-10, kringle V and the protease domain and a 46 kb SwaI fragment, spanning kringles IV 5-10, kringle V and the protease domain was demonstrated by PFGE/Southern blotting in 30 unrelated subjects, who represented a range of apo(a) size alleles containing from 11 to 49 kringles. Our analysis demonstrates that the number of kringles IV 3-10 is invariable in the human apo(a) gene, suggesting that the 3' domain of Apo(a) is functionally important. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:253 / 258
页数:6
相关论文
共 20 条
[1]   CYS4057 OF APOLIPOPROTEIN(A) IS ESSENTIAL FOR LIPOPROTEIN(A) ASSEMBLY [J].
BRUNNER, C ;
KRAFT, HG ;
UTERMANN, G ;
MULLER, HJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11643-11647
[2]   THE HUMAN APOLIPOPROTEIN(A) PLASMINOGEN GENE-CLUSTER CONTAINS A NOVEL HOMOLOG TRANSCRIBED IN LIVER [J].
BYRNE, CD ;
SCHWARTZ, K ;
MEER, K ;
CHENG, JF ;
LAWN, RM .
ARTERIOSCLEROSIS AND THROMBOSIS, 1994, 14 (04) :534-541
[3]   IDENTIFICATION OF 2 FUNCTIONALLY DISTINCT LYSINE-BINDING SITES IN KRINGLE-37 AND IN KRINGLES 32-36 OF HUMAN APOLIPOPROTEIN(A) [J].
ERNST, A ;
HELMHOLD, M ;
BRUNNER, C ;
PETHOSCHRAMM, A ;
ARMSTRONG, VW ;
MULLER, HJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :6227-6234
[4]   STRUCTURAL REQUIREMENTS OF APO-A FOR THE LIPOPROTEIN-A ASSEMBLY [J].
FRANK, S ;
DUROVIC, S ;
KOSTNER, GM .
BIOCHEMICAL JOURNAL, 1994, 304 :27-30
[5]   MULTIPLE MEMBERS OF THE PLASMINOGEN APOLIPOPROTEIN(A) GENE FAMILY ASSOCIATED WITH THROMBOSIS [J].
ICHINOSE, A .
BIOCHEMISTRY, 1992, 31 (12) :3113-3118
[6]  
KOSCHINSKY ML, 1993, J BIOL CHEM, V268, P19819
[7]  
KRAFT HG, 1992, HUM GENET, V90, P220
[8]   MOLECULAR DEFINITION OF THE EXTREME SIZE POLYMORPHISM IN APOLIPOPROTEIN(A) [J].
LACKNER, C ;
COHEN, JC ;
HOBBS, HH .
HUMAN MOLECULAR GENETICS, 1993, 2 (07) :933-940
[9]   MOLECULAR-BASIS OF APOLIPOPROTEIN-(A) ISOFORM SIZE HETEROGENEITY AS REVEALED BY PULSED-FIELD GEL-ELECTROPHORESIS [J].
LACKNER, C ;
BOERWINKLE, E ;
LEFFERT, CC ;
RAHMIG, T ;
HOBBS, HH .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (06) :2153-2161
[10]   Apolipoprotein(a): A puzzling evolutionary story [J].
Lawn, R ;
Patthy, L ;
Pesole, G ;
Saccone, C .
JOURNAL OF MOLECULAR EVOLUTION, 1997, 44 (02) :234-236