Analysis of Human CD36 Gene Sequence Alterations in the Oxidized Low-Density Lipoprotein-Binding Region Using Denaturing High-Performance Liquid Chromatography

被引:8
作者
Rac, Monika Ewa [1 ]
Suchy, Janina [2 ]
Kurzawski, Grzegorz [2 ]
Safranow, Krzysztof [1 ]
Jakubowska, Katarzyna [1 ]
Olszewska, Maria [1 ]
Garanty-Bogacka, Barbara [3 ]
Rac, Michal [4 ]
Poncyljusz, Wojciech [5 ]
Chlubek, Dariusz [1 ]
机构
[1] Pomeranian Med Univ, Dept Biochem & Med Chem, PL-70111 Szczecin, Poland
[2] Pomeranian Med Univ, Dept Genet & Pathol, PL-70111 Szczecin, Poland
[3] Pomeranian Med Univ, Independent Lab Propedeut Pediat, PL-70111 Szczecin, Poland
[4] Pomeranian Med Univ, Dept Diagnost Imaging & Intervent Radiol, PL-70111 Szczecin, Poland
[5] Pomeranian Med Univ, Dept Intervent Radiol, PL-70111 Szczecin, Poland
关键词
SCAVENGER RECEPTOR; MUTATION ANALYSIS; ICD36; DEFICIENCY; MELTING ANALYSIS; MOLECULAR-BASIS; ATHEROSCLEROSIS; CHOLESTEROL; VARIANTS; DHPLC; IDENTIFICATION;
D O I
10.1089/gtmb.2010.0031
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
Denaturing high-performance liquid chromatography (DHPLC) has been employed as a prescreening tool to reduce the amount of DNA sequencing. It could be a simple and cost-effective screening method for mutations and polymorphisms in exons 4, 5, and 6 of the CD36 gene, which encode the protein region responsible for the removal of oxidized low-density lipoprotein. Genomic DNA was isolated from 306 Caucasian infants of Polish origin. Six single-nucleotide substitutions were detected by DHPLC and confirmed by direct sequencing. The A591T, G550A, and C572T alterations have not been described so far. Each of two nonsynonymous substitutions (Asp184Asn, Pro191Leu) was found in one subject (0.2% minor allele frequency). The results suggest that nonsynonymous alterations in the analyzed CD36 region are rare in Caucasians. DHPLC is a specific and cost-effective technique that may prove to be particularly useful for the identification of polymorphisms and mutations in the CD36 gene.
引用
收藏
页码:551 / 557
页数:7
相关论文
共 37 条
  • [1] [Anonymous], 2009, CLEVE CLIN J MED, DOI DOI 10.3949/CCJM.76.S2.06
  • [2] Reversible binding of long-chain fatty acids to purified FAT, the adipose CD36 homolog
    Baillie, AGS
    Coburn, CT
    Abumrad, NA
    [J]. JOURNAL OF MEMBRANE BIOLOGY, 1996, 153 (01) : 75 - 81
  • [3] CD36 deficiency protects against malarial anaemia in children by reducing Plasmodium falciparum-infected red blood cell adherence to vascular endothelium
    Chilongola, Jaffu
    Balthazary, Sakurani
    Mpina, Maximillian
    Mhando, Martin
    Mbugi, Erasto
    [J]. TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2009, 14 (07) : 810 - 816
  • [4] Using CCM and DHPLC to detect mutations in the glucocorticoid receptor in atherosclerosis: a comparison
    Cotton, RGH
    Bray, PJ
    [J]. JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2001, 47 (1-2): : 91 - 100
  • [5] Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency
    Fasano, T
    Bocchi, L
    Pisciotta, L
    Bertolini, S
    Calandra, S
    [J]. JOURNAL OF LIPID RESEARCH, 2005, 46 (04) : 817 - 822
  • [6] GENE ENCODING THE COLLAGEN TYPE-I AND THROMBOSPONDIN RECEPTOR CD36 IS LOCATED ON CHROMOSOME-7Q11.2
    FERNANDEZRUIZ, E
    ARMESILLA, AL
    SANCHEZMADRID, F
    VEGA, MA
    [J]. GENOMICS, 1993, 17 (03) : 759 - 761
  • [7] Positive selection of a CD36 nonsense variant in sub-Saharan Africa, but no association with severe malaria phenotypes
    Fry, Andrew E.
    Ghansa, Anita
    Small, Kerrin S.
    Palma, Alejandro
    Auburn, Sarah
    Diakite, Mahamadou
    Green, Angela
    Campino, Susana
    Teo, Yik Y.
    Clark, Taane G.
    Jeffreys, Anna E.
    Wilson, Jonathan
    Jallow, Muminatou
    Sisay-Joof, Fatou
    Pinder, Margaret
    Griffiths, Michael J.
    Peshu, Norbert
    Williams, Thomas N.
    Newton, Charles R.
    Marsh, Kevin
    Molyneux, Malcolm E.
    Taylor, Terrie E.
    Koram, Kwadwo A.
    Oduro, Abraham R.
    Rogers, William O.
    Rockett, Kirk A.
    Sabeti, Pardis C.
    Kwiatkowski, Dominic P.
    [J]. HUMAN MOLECULAR GENETICS, 2009, 18 (14) : 2683 - 2692
  • [8] GREENWALT DE, 1992, BLOOD, V80, P1105
  • [9] PERFORMING THE EXACT TEST OF HARDY-WEINBERG PROPORTION FOR MULTIPLE ALLELES
    GUO, SW
    THOMPSON, EA
    [J]. BIOMETRICS, 1992, 48 (02) : 361 - 372
  • [10] Identification of cryptic splice site, exon skipping, and novel point mutations in type ICD36 deficiency
    Hanawa, H
    Watanabe, K
    Nakamura, T
    Ogawa, Y
    Toba, K
    Fuse, I
    Kodama, M
    Kato, K
    Fuse, K
    Aizawa, Y
    [J]. JOURNAL OF MEDICAL GENETICS, 2002, 39 (04) : 286 - 291