Mutation Scanning

Analyzing Genetic Variation Using HRM Mutation Scanning Followed by Sanger Sequencing

Mutation scanning strategies seek to quickly and efficiently scan DNA samples from many individuals for minor genetic variations to identify candidates with genetic variations for full sequencing analysis.

HRM Analysis for Fast, Accurate & Reliable Mutation

Use high resolution melt (HRM) analysis to scan large numbers of samples for genetic variation. With the introduction of brighter DNA binding dyes, real-time PCR instruments that collect fluorescence data at finer temperature resolution, and intuitive software platforms, high resolution melt (HRM) analysis is becoming the method of choice for scanning large numbers of samples for genetic variants.

Compared to other technologies for mutation scanning, such as pyrosequencing, denaturing HPLC (dHPLC), and denaturing gradient gel electrophoresis (DGGE), HRM offers:
  • A far easier and faster procedure that consumes significantly less reagent
  • Higher reproducibility
  • Reduced optimization and interpretation efforts
  • Better accuracy and sensitivity
  • A closed tube procedure reducing the risk of cross-contamination of samples

Figure 1 (Right): Difference Plot of a human 121 bp region in NAT2 that was amplified from 4 replicates of 24 samples.

 

Non-Destructive and Well-Suited for Variant Scanning

Select samples with HRM melt profiles that are significantly different from those of wild-type samples for further study. For example, the PCR reaction product from HRM can be introduced directly into the Sanger sequencing reaction for DNA sequencing.

Sanger DNA sequencing remains the most straightforward, reliable method for determining the precise genetic sequence of DNA fragments.

Mutation Scanning Experimental Workflow

A critical first step in setting up mutation scanning experiments using HRM analysis is to design PCR primers to amplify overlapping segments of the genomic region of interest. Important considerations for the primer design step include designing appropriately sized amplicons and observing well established conventions for designing high-quality PCR primers.

HRM analysis works well with amplicons in the ~120–300 bp size range; this size corresponds to 80–250 bp genomic DNA targets amplified using ~20–40 nt PCR primers. Amplicons in this range are sufficiently short to yield simple, easily analyzed melt profiles, yet long enough to minimize the number of individual amplicons needed to cover the target region. Large sequence variations may be detectable in amplicons longer than ~300 bp; however, more subtle variations such as A/T class 4 SNPs, are typically detectable only in smaller amplicons.

Recommended Products

 

Primer Express Software
Allows you to design your own primers and probes using TaqMan® and SYBR® Green I dye chemistries for gene quantitation and allelic discrimination (SNP) real-time PCR applications.