New applications and developments in the use of multiplex ligation-dependent probe amplification

被引:67
作者
Kozlowski, Piotr [1 ]
Jasinska, Anna J. [2 ]
Kwiatkowski, David J. [3 ]
机构
[1] Polish Acad Sci, Inst Bioorgan Chem, Canc Genet Lab, PL-61704 Poznan, Poland
[2] Univ Calif Los Angeles, Ctr Neurobehav Genet, Los Angeles, CA USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Translat Med,Dept Med, Boston, MA 02115 USA
关键词
Copy number variation; Expression profiling; Multiplex ligation-dependent probe amplification; Mutation detection; Transgene genotyping;
D O I
10.1002/elps.200800126
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Multiplex ligation-dependent probe amplification (MLPA) is a commonly used technique for determining relative DNA sequence dosage (or copy number) in a complex DNA sample. Originally MLPA was designed as a copy number analysis tool for detecting disease-causing genomic mutations and has been successfully applied in the testing and identification of hundreds of genomic mutations in numerous genes including DMD, BRCA1, NF1, and TSC2. More recently, several modifications of the original technique have been implemented. Arguably the most important enhancement of MLPA has been probe generation by chemical synthesis, enabling the facile creation of novel probe sets for any desired application. Other newer applications of MLPA include methylation status determination, copy number analysis in segmentally duplicated regions, expression profiling, and transgene genotyping. MLPA has a potential major role in the analysis of common copy number variation in genome-wide association analyses, which may be enhanced by future improvements to increase throughput and lower costs, such as array-MLPA.
引用
收藏
页码:4627 / 4636
页数:10
相关论文
共 86 条
[1]   Large genomic deletions inactivate the BRCA2 gene in breast cancer families [J].
Agata, S ;
Dalla Palma, M ;
Callegaro, M ;
Scaini, MC ;
Menin, C ;
Ghiotto, C ;
Nicoletto, O ;
Zavagno, G ;
Chieco-Bianchi, L ;
D'Andrea, E ;
Montagna, M .
JOURNAL OF MEDICAL GENETICS, 2005, 42 (10) :e64
[2]   Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans [J].
Aitman, TJ ;
Dong, R ;
Vyse, TJ ;
Norsworthy, PJ ;
Johnson, MD ;
Smith, J ;
Mangion, J ;
Roberton-Lowe, C ;
Marshall, AJ ;
Petretto, E ;
Hodges, MD ;
Bhangal, G ;
Patel, SG ;
Sheehan-Rooney, K ;
Duda, M ;
Cook, PR ;
Evans, DJ ;
Domin, J ;
Flint, J ;
Boyle, JJ ;
Pusey, CD ;
Cook, HT .
NATURE, 2006, 439 (7078) :851-855
[3]   Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH [J].
Akrami, SM ;
Dunlop, MG ;
Farrington, SM ;
Frayling, IM ;
MacDonald, F ;
Harvey, JF ;
Armour, JAL .
FAMILIAL CANCER, 2005, 4 (02) :145-149
[4]   High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome [J].
Aretz, S ;
Stienen, D ;
Uhlhaas, S ;
Loff, S ;
Back, W ;
Pagenstecher, C ;
McLeod, DR ;
Graham, GE ;
Mangold, E ;
Santer, R ;
Propping, P ;
Friedl, W .
HUMAN MUTATION, 2005, 26 (06) :513-519
[5]   Measurement of locus copy number by hybridisation with amplifiable probes [J].
Armour, JAL ;
Sismani, C ;
Patsalis, PC ;
Cross, G .
NUCLEIC ACIDS RESEARCH, 2000, 28 (02) :605-609
[6]   Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats [J].
Armour, John A. L. ;
Palla, Raquel ;
Zeeuwen, Patrick L. J. M. ;
den Heijer, Martin ;
Schalkwijk, Joost ;
Hollox, Edward J. .
NUCLEIC ACIDS RESEARCH, 2007, 35 (03)
[7]   Real-time quantitative PCR-based system for determining transgene copy number in transgenic animals [J].
Ballester, M ;
Castelló, A ;
Ibáñez, E ;
Sánchez, A ;
Folch, JM .
BIOTECHNIQUES, 2004, 37 (04) :610-613
[8]   Homologues to the first gene for autosomal dominant polycystic kidney disease are pseudogenes [J].
Bogdanova, N ;
Markoff, A ;
Gerke, V ;
McCluskey, M ;
Horst, J ;
Dworniczak, B .
GENOMICS, 2001, 74 (03) :333-341
[9]   Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene [J].
Bunyan, David J. ;
Skinner, Alison C. ;
Ashton, Emma J. ;
Sillibourne, Julie ;
Brown, Tom ;
Collins, Amanda L. ;
Cross, Nicholas C. P. ;
Harvey, John F. ;
Robinson, David O. .
MOLECULAR BIOTECHNOLOGY, 2007, 35 (02) :135-140
[10]   Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification [J].
Bunyan, DJ ;
Eccles, DM ;
Sillibourne, J ;
Wilkins, E ;
Thomas, NS ;
Shea-Simonds, J ;
Duncan, PJ ;
Curtis, CE ;
Robinson, DO ;
Harvey, JF ;
Cross, NCP .
BRITISH JOURNAL OF CANCER, 2004, 91 (06) :1155-1159