EXPRESSION OF MESSENGER-RNA FOR MATRIX GAMMA-CARBOXYGLUTAMIC ACID PROTEIN DURING PROGRESSION OF ATHEROSCLEROSIS IN AORTAE OF WATANABE HERITABLE HYPERLIPIDEMIC RABBITS

被引:6
作者
SOHMA, Y
SUZUKI, T
SASANO, H
NAGURA, H
NOSE, M
YAMAMOTO, T
机构
[1] TOHOKU UNIV,GENE RES CTR,AOBA KU,SENDAI,MIYAGI 981,JAPAN
[2] KIRIN BREWERY CO LTD,PHARMACEUT RES LAB,MAEBASHI,GUMMA 371,JAPAN
[3] TOHOKU UNIV,SCH MED,DEPT PATHOL,AOBA KU,SENDAI,MIYAGI 981,JAPAN
关键词
ATHEROSCLEROSIS; DIFFERENTIAL HYBRIDIZATION; MATRIX GAMMA-CARBOXYGLUTAMIC ACID PROTEIN; WATANABE HERITABLE HYPERLIPIDEMIC RABBIT;
D O I
10.1093/oxfordjournals.jbchem.a124591
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
In an effort to characterize mRNAs that are highly expressed during atherosclerosis, we employed differential hybridization screening of a cDNA library constructed from total RNA derived from the aorta of Watanabe heritable hyperlipidemic (WHHL) rabbits. Characterizing the cDNAs for mRNAs that are present in large amounts in WHHL rabbit aortae, we identified a positive clone encoding matrix gamma-carboxyglutamic acid protein (MGP). The primary structure of rabbit MGP was deduced from nucleotide sequence analysis of the cDNA. Northern blot analysis of total RNA prepared from aortae of WHHL and normal rabbits of various ages indicated that the expression of MGP mRNA increased in proportion to the progression of atherosclerosis in WHHL rabbits. Analysis of MGP mRNA by in situ hybridization revealed that a significant amount of MGP mRNA is accumulated in atherosclerotic lesions of WHHL rabbits, suggesting that the expression of MGP mRNA is correlated with the progression of atherosclerosis.
引用
收藏
页码:747 / 751
页数:5
相关论文
共 28 条
[1]   A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
SCIENCE, 1986, 232 (4746) :34-47
[2]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[3]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[4]  
FRASER JD, 1988, J BIOL CHEM, V263, P11033
[5]  
Goldstein J.L., 1989, METABOLIC BASIS INHE, P1215
[6]   A SIMPLE AND VERY EFFICIENT METHOD FOR GENERATING CDNA LIBRARIES [J].
GUBLER, U ;
HOFFMAN, BJ .
GENE, 1983, 25 (2-3) :263-269
[7]   COMPLEMENTARY-DNA FOR HUMAN T-CELL CYCLOPHILIN [J].
HAENDLER, B ;
HOFERWARBINEK, R ;
HOFER, E .
EMBO JOURNAL, 1987, 6 (04) :947-950
[8]  
HALE JE, 1988, J BIOL CHEM, V263, P580
[9]  
HAYASHI M, 1988, DEVELOPMENT, V103, P27
[10]  
IKEDA T, 1991, J BONE MINER RES, V6, P1013