Detection of ApoE E2, E3 and E4 alleles using MALDI-TOF mass spectrometry and the homogeneous mass-extend technology -: art. no. e149

被引:69
作者
Ghebranious, N [1 ]
Ivacic, L [1 ]
Mallum, J [1 ]
Dokken, C [1 ]
机构
[1] Marshfield Clin Fdn Med Res & Educ, Mol Diagnost Genotyping Lab, Marshfield, WI 54449 USA
关键词
D O I
10.1093/nar/gni155
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
Apolipoprotein (Apo) E is one of the five main types of blood lipoproteins (A-E). It is synthesized primarily in the liver and brain and helps in transporting lipids from one place to another as well as facilitates the clearing of dietary fats, such as triglycerides, from the blood. The ApoE gene exists in three different forms: E2, E3 and E4. E3 is considered to be the normal form. Variants of the ApoE gene have been associated with various diseases. Developing an assay for the genotyping of ApoE variants for use both in clinical and large cohort based association settings would be extremely valuable and would require the use of a platform that has high-throughput capabilities and is highly accurate. Here we describe an assay for the simultaneous genotyping of the ApoE variants in a single bi-plex reaction and a single well using the matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry and the homogeneous mass-extend (hME) technology. The assay is robust, highly accurate and suitable for both clinical applications and for the genotyping of large disease cohorts. Moreover, the prevalence of ApoE variants in a cohort of Caucasians from the central Wisconsin area is outlined.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 35 条
[1]   Optimization of apolipoprotein E genotyping [J].
Addya, K ;
Wang, YL ;
Leonard, DGB .
MOLECULAR DIAGNOSIS, 1997, 2 (04) :271-276
[2]   Molecular diagnosis of familial adenomatous polyposis (FAP):: Genotyping of adenomatous polyposis coli (APC) alleles by MALDI-TOF mass spectrometry [J].
Bonk, T ;
Humeny, A ;
Sutter, C ;
Gebert, J ;
Doeberitz, MV ;
Becker, CM .
CLINICAL BIOCHEMISTRY, 2002, 35 (02) :87-92
[3]   High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: Practice, problems and promise [J].
Bray, MS ;
Boerwinkle, E ;
Doris, PA .
HUMAN MUTATION, 2001, 17 (04) :296-304
[4]  
BRESLOW JL, 1982, J LIPID RES, V23, P1224
[5]   Use of MALDI-TOF mass spectrometry in a 51-mutation test for cystic fibrosis: Evidence that 3199del6 is a disease-causing mutation [J].
Buyse, IM ;
McCarthy, SE ;
Lurix, P ;
Pace, RP ;
Vo, D ;
Bartlett, GA ;
Schmitt, ES ;
Ward, PA ;
Oermann, C ;
Eng, CM ;
Roa, BB .
GENETICS IN MEDICINE, 2004, 6 (05) :426-430
[6]   A simple and efficient method for apolipoprotein E genotype determination [J].
Chapman, J ;
Estupinan, J ;
Asherov, A ;
Goldfarb, LG .
NEUROLOGY, 1996, 46 (05) :1484-1485
[7]   Apo E variants in patients with type III hyperlipoproteinemia [J].
Civeira, F ;
Pocovi, M ;
Cenarro, A ;
Casao, E ;
Vilella, E ;
Joven, J ;
Gonzalez, J ;
GarciaOtin, AL ;
Ordovas, JM .
ATHEROSCLEROSIS, 1996, 127 (02) :273-282
[8]   Apolipoprotein E (APOE) allele distribution in the world.: Is APOE*4 a 'thrifty' allele? [J].
Corbo, RM ;
Scacchi, R .
ANNALS OF HUMAN GENETICS, 1999, 63 :301-310
[9]   GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES [J].
CORDER, EH ;
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, DE ;
GASKELL, PC ;
SMALL, GW ;
ROSES, AD ;
HAINES, JL ;
PERICAKVANCE, MA .
SCIENCE, 1993, 261 (5123) :921-923
[10]   High throughput screening of genetic polymorphisms by matrix-assisted laser desorption ionization time-of-flight mass spectrometry [J].
Corona, G ;
Toffoli, G .
COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2004, 7 (08) :707-725