Research Papers:

Significant impact of amount of PCR input templates on various PCR-based DNA methylation analysis and countermeasure

Zhaojun Liu, Jing Zhou, Liankun Gu and Dajun Deng _

PDF  |  HTML  |  How to cite  |  Order a Reprint

Oncotarget. 2016; 7:56447-56455. https://doi.org/10.18632/oncotarget.10906

Metrics: PDF 1603 views  |   HTML 2102 views  |   ?  


Zhaojun Liu1,*, Jing Zhou1,*, Liankun Gu1, Dajun Deng1

1Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Division of Etiology, Peking University Cancer Hospital and Institute, Haidian District, Beijing, 100142, China

*These authors contributed equally to this work

Correspondence to:

Dajun Deng, email: dengdajun@bjmu.edu.cn

Keywords: DNA methylation, false negative detection, MethyLight, DHPLC, MSP

Received: June 06, 2016     Accepted: July 20, 2016     Published: July 28, 2016


Methylation changes of CpG islands can be determined using PCR-based assays. However, the exact impact of the amount of input templates (TAIT) on DNA methylation analysis has not been previously recognized. Using COL2A1 gene as an input reference, TAIT difference between human tissues with methylation-positive and –negative detection was calculated for two representative genes GFRA1 and P16. Results revealed that TAIT in GFRA1 methylation-positive frozen samples (n = 332) was significantly higher than the methylation-negative ones (n = 44) (P < 0.001). Similar difference was found in P16 methylation analysis. The TAIT-related effect was also observed in methylation-specific PCR (MSP) and denatured high performance liquid chromatography (DHPLC) analysis. Further study showed that the minimum TAIT for a successful MethyLight PCR reaction should be ≥ 9.4 ng (CtCOL2A1 ≤ 29.3), when the cutoff value of the methylated-GFRA1 proportion for methylation-positive detection was set at 1.6%. After TAIT of the methylation non-informative frozen samples (n = 94; CtCOL2A1 > 29.3) was increased above the minimum TAIT, the methylation-positive rate increased from 72.3% to 95.7% for GFRA1 and 26.6% to 54.3% for P16, respectively (Ps < 0.001). Similar results were observed in the FFPE samples. In conclusion, TAIT critically affects results of various PCR-based DNA methylation analyses. Characterization of the minimum TAIT for target CpG islands is essential to avoid false-negative results.

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 10906