APOLIPOPROTEIN(A) SIZE HETEROGENEITY IS RELATED TO VARIABLE NUMBER OF REPEAT SEQUENCES IN ITS MESSENGER-RNA

被引:143
作者
KOSCHINSKY, ML
BEISIEGEL, U
HENNEBRUNS, D
EATON, DL
LAWN, RM
机构
[1] GENENTECH INC,DEPT CARDIOVASC RES,460 POINT SAN BRUNO BLVD,SAN FRANCISCO,CA 94080
[2] UNIV HAMBURG,DEPT MED & SURG,W-2000 HAMBURG 20,GERMANY
关键词
D O I
10.1021/bi00455a007
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
Plasma apolipoprotein(a) [apo(a)] shows considerable size heterogeneity, existing as discrete glycoprotein isoform variants that range in apparent molecular mass from approximately 400 to 800 kDa. To study the molecular basis of protein size variability, we have isolated liver RNA from individuals with different apo(a) isoforms, and identified apo(a)-specific transcripts using Northern blot analysis. Transcript sizes were shown to be variable (8.0-12 kb) and in all cases were closely correlated with protein masses (590–850 kDa) as determined from immunoblots. Thus, it is almost certain that apo(a) isoform size variation is due to allelic differences in the number of its tandemly repeated sequences of 114 amino acids that resemble kringle four of plasminogen. The high carbohydrate content of apo(a) makes true molecular weight estimations in SDS-PAGE gels difficult. However, a recombinant form of apo(a) containing 17 kringle repeats (calculated molecular mass of 250 kDa) migrates on SDS-PAGE gels only slightly below apoB-100, with an apparent molecular mass of approximately 500 kDa. Since smaller protein isoforms have been observed in the population, this suggests that plasma apo(a) isoforms contain from less than 17 to greater than 30 tandemly repeated kringle units. © 1990, American Chemical Society. All rights reserved.
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页码:640 / 644
页数:5
相关论文
共 31 条
[1]  
ARMSTRONG VW, 1985, J LIPID RES, V26, P1314
[2]   A METHOD FOR ISOLATION OF INTACT, TRANSLATIONALLY ACTIVE RIBONUCLEIC-ACID [J].
CATHALA, G ;
SAVOURET, JF ;
MENDEZ, B ;
WEST, BL ;
KARIN, M ;
MARTIAL, JA ;
BAXTER, JD .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1983, 2 (04) :329-335
[3]  
CHEN SH, 1986, J BIOL CHEM, V261, P2918
[4]   ASSOCIATION OF LEVELS OF LIPOPROTEIN LP(A), PLASMA-LIPIDS, AND OTHER LIPOPROTEINS WITH CORONARY-ARTERY DISEASE DOCUMENTED BY ANGIOGRAPHY [J].
DAHLEN, GH ;
GUYTON, JR ;
ATTAR, M ;
FARMER, JA ;
KAUTZ, JA ;
GOTTO, AM .
CIRCULATION, 1986, 74 (04) :758-765
[5]   GENETIC-LINKAGE BETWEEN LIPOPROTEIN(A) PHENOTYPE AND A DNA POLYMORPHISM IN THE PLASMINOGEN GENE [J].
DRAYNA, DT ;
HEGELE, RA ;
HASS, PE ;
EMI, M ;
WU, LL ;
EATON, DL ;
LAWN, RM ;
WILLIAMS, RR ;
WHITE, RL ;
LALOUEL, JM .
GENOMICS, 1988, 3 (03) :230-236
[6]  
DURRINGTON PN, 1988, LANCET, V1, P1070
[7]   PARTIAL AMINO-ACID-SEQUENCE OF APOLIPOPROTEIN(A) SHOWS THAT IT IS HOMOLOGOUS TO PLASMINOGEN [J].
EATON, DL ;
FLESS, GM ;
KOHR, WJ ;
MCLEAN, JW ;
XU, QT ;
MILLER, CG ;
LAWN, RM ;
SCANU, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) :3224-3228
[8]  
FEINBERG A, 1982, ANAL BIOCHEM, V132, P6
[9]  
FLESS GM, 1984, J BIOL CHEM, V259, P1470
[10]  
FLESS GM, 1985, J LIPID RES, V26, P1224