Improved PCR based methods for detecting C9orf72 hexanucleotide repeat expansions

被引:34
作者
Cleary, Elaine M. [1 ,2 ]
Pal, Suvankar [2 ,3 ]
Azam, Tara [1 ]
Moore, David J. [1 ]
Swingler, Robert [2 ]
Gorrie, George [2 ]
Stephenson, Laura [2 ,3 ]
Colville, Shuna [2 ,3 ]
Chandran, Siddharthan [2 ,3 ]
Porteous, Mary [1 ,2 ]
Warner, Jon P. [1 ]
机构
[1] Western Gen Hosp, South East Scotland Genet Serv, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Euan Macdonald Ctr MND Res, 49 Little France Crescent, Edinburgh EH16 4SB, Midlothian, Scotland
[3] Univ Edinburgh, Anne Rowling Regenerat Neurol Clin, 49 Little France Crescent, Edinburgh EH16 4SB, Midlothian, Scotland
关键词
C9orf72; Repeat-primed PCR; Amyotrophic lateral sclerosis; Genetic testing; ALS; DIAGNOSIS;
D O I
10.1016/j.mcp.2016.06.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Due to the GC-rich, repetitive nature of C9orf72 hexanucleotide repeat expansions, PCR based detection methods are challenging. Several limitations of PCR have been reported and overcoming these could help to define the pathogenic range. There is also a need to develop improved repeat-primed PCR assays which allow detection even in the presence of genomic variation around the repeat region. We have optimised PCR conditions for the C9orf72 hexanucleotide repeat expansion, using betaine as a co-solvent and specific cycling conditions, including slow ramping and a high denaturation temperature. We have developed a flanking assay, and repeat-primed PCR assays for both 3' and 5' ends of the repeat expansion, which when used together provide a robust strategy for detecting the presence or absence of expansions greater than 100 repeats, even in the presence of genomic variability at the 3' end of the repeat. Using our assays, we have detected repeat expansions in 47/442 Scottish ALS patients. Furthermore, we recommend the combined use of these assays in a clinical diagnostic setting. (C) 2016 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:218 / 224
页数:7
相关论文
共 19 条
[11]   Expandable DNA repeats and human disease [J].
Mirkin, Sergei M. .
NATURE, 2007, 447 (7147) :932-940
[12]   Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD [J].
Nordin, Angelica ;
Akimoto, Chizuru ;
Wuolikainen, Anna ;
Alstermark, Helena ;
Jonsson, Par ;
Birve, Anna ;
Marklund, Stefan L. ;
Graffmo, Karin S. ;
Forsberg, Karin ;
Brannstrom, Thomas ;
Andersen, Peter M. .
HUMAN MOLECULAR GENETICS, 2015, 24 (11) :3133-3142
[13]   Multiple Heat Pulses during PCR Extension Enabling Amplification of GC-Rich Sequences and Reducing Amplification Bias [J].
Orpana, Art K. ;
Ho, Tho H. ;
Stenman, Jakob .
ANALYTICAL CHEMISTRY, 2012, 84 (04) :2081-2087
[14]   A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD [J].
Renton, Alan E. ;
Majounie, Elisa ;
Waite, Adrian ;
Simon-Sanchez, Javier ;
Rollinson, Sara ;
Gibbs, J. Raphael ;
Schymick, Jennifer C. ;
Laaksovirta, Hannu ;
van Swieten, John C. ;
Myllykangas, Liisa ;
Kalimo, Hannu ;
Paetau, Anders ;
Abramzon, Yevgeniya ;
Remes, Anne M. ;
Kaganovich, Alice ;
Scholz, Sonja W. ;
Duckworth, Jamie ;
Ding, Jinhui ;
Harmer, Daniel W. ;
Hernandez, Dena G. ;
Johnson, Janel O. ;
Mok, Kin ;
Ryten, Mina ;
Trabzuni, Danyah ;
Guerreiro, Rita J. ;
Orrell, Richard W. ;
Neal, James ;
Murray, Alex ;
Pearson, Justin ;
Jansen, Iris E. ;
Sondervan, David ;
Seelaar, Harro ;
Blake, Derek ;
Young, Kate ;
Halliwell, Nicola ;
Callister, Janis Bennion ;
Toulson, Greg ;
Richardson, Anna ;
Gerhard, Alex ;
Snowden, Julie ;
Mann, David ;
Neary, David ;
Nalls, Michael A. ;
Peuralinna, Terhi ;
Jansson, Lilja ;
Isoviita, Veli-Matti ;
Kaivorinne, Anna-Lotta ;
Holtta-Vuori, Maarit ;
Ikonen, Elina ;
Sulkava, Raimo .
NEURON, 2011, 72 (02) :257-268
[15]   A small deletion in C9orf72 hides a proportion of expansion carriers in FTLD [J].
Rollinson, Sara ;
Callister, Janis Bennion ;
Young, Kate ;
Ryan, Sarah J. ;
Druyeh, Ronald ;
Rohrer, Jonathan D. ;
Snowden, Julie ;
Richardson, Anna ;
Jones, Matt ;
Harris, Jenny ;
Davidson, Yvonne ;
Robinson, Andrew ;
Ealing, John ;
Johnson, Janel O. ;
Traynor, Bryan ;
Mead, Simon ;
Mann, David ;
Pickering-Brown, Stuart M. .
NEUROBIOLOGY OF AGING, 2015, 36 (03) :1601.e1-e5
[16]   Association between repeat sizes and clinical and pathological characteristics in carriers of C90RF72 repeat expansions (Xpansize-72): a cross-sectional cohort study [J].
van Blitterswijk, Marka ;
Dejesus-Hernandez, Mariely ;
Niemantsverdriet, Ellis ;
Murray, Melissa E. ;
Heckman, Michael G. ;
Diehl, Nancy N. ;
Brown, Patricia H. ;
Baker, Matthew C. ;
Finch, NiCole A. ;
Bauer, Peter O. ;
Serrano, Geidy ;
Beach, Thomas G. ;
Josephs, Keith A. ;
Knopman, David S. ;
Petersen, Ronald C. ;
Boeve, Bradley F. ;
Graff-Radford, Neill R. ;
Boylan, Kevin B. ;
Petrucelli, Leonard ;
Dickson, Dennis W. ;
Rademakers, Rosa .
LANCET NEUROLOGY, 2013, 12 (10) :978-988
[17]   A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats [J].
van der Zee, Julie ;
Gijselinck, Ilse ;
Dillen, Lubina ;
Van Langenhove, Tim ;
Theuns, Jessie ;
Engelborghs, Sebastiaan ;
Philtjens, Stephanie ;
Vandenbulcke, Mathieu ;
Sleegers, Kristel ;
Sieben, Anne ;
Baumer, Veerle ;
Maes, Githa ;
Corsmit, Ellen ;
Borroni, Barbara ;
Padovani, Alessandro ;
Archetti, Silvana ;
Perneczky, Robert ;
Diehl-Schmid, Janine ;
de Mendonca, Alexandre ;
Miltenberger-Miltenyi, Gabriel ;
Pereira, Sonia ;
Pimentel, Jose ;
Nacmias, Benedetta ;
Bagnoli, Silvia ;
Sorbi, Sandro ;
Graff, Caroline ;
Chiang, Huei-Hsin ;
Westerlund, Marie ;
Sanchez-Valle, Raquel ;
Llado, Albert ;
Gelpi, Ellen ;
Santana, Isabel ;
Almeida, Maria Rosario ;
Santiago, Beatriz ;
Frisoni, Giovanni ;
Zanetti, Orazio ;
Bonvicini, Cristian ;
Synofzik, Matthis ;
Maetzler, Walter ;
vom Hagen, Jennifer Mueller ;
Schoels, Ludger ;
Heneka, Michael T. ;
Jessen, Frank ;
Matej, Radoslav ;
Parobkova, Eva ;
Kovacs, Gabor G. ;
Stroebel, Thomas ;
Sarafov, Stayko ;
Tournev, Ivailo ;
Jordanova, Albena .
HUMAN MUTATION, 2013, 34 (02) :363-373
[18]   A general method for the detection of large CAG repeat expansions by fluorescent PCR [J].
Warner, JP ;
Barron, LH ;
Goudie, D ;
Kelly, K ;
Dow, D ;
Fitzpatrick, DR ;
Brock, DJH .
JOURNAL OF MEDICAL GENETICS, 1996, 33 (12) :1022-1026
[19]   Jump from Pre-mutation to Pathologic Expansion in C9orf72 [J].
Xi, Zhengrui ;
van Blitterswijk, Marka ;
Zhang, Ming ;
McGoldrick, Philip ;
McLean, Jesse R. ;
Yunusova, Yana ;
Knock, Erin ;
Moreno, Danielle ;
Sato, Christine ;
McKeever, Paul M. ;
Schneider, Raphael ;
Keith, Julia ;
Petrescu, Nicolae ;
Fraser, Paul ;
Tartaglia, Maria Carmela ;
Baker, Matthew C. ;
Graff-Radford, Neill R. ;
Boylan, Kevin B. ;
Dickson, Dennis W. ;
Mackenzie, Ian R. ;
Rademakers, Rosa ;
Robertson, Janice ;
Zinman, Lorne ;
Rogaeva, Ekaterina .
AMERICAN JOURNAL OF HUMAN GENETICS, 2015, 96 (06) :962-970