Abstract
Background: The ACP1 gene, encoding a low-molecular-weight
phosphotyrosine phosphatase (LMW-PTP), has been suggested as a common
genetic factor of several human diseases, including inflammatory and
autoimmune diseases, favism and tumors. For this reason, the ACP1 enzyme
has been investigated by case-control studies for decades. Initially
based on protein electrophoresis, the ACP1 phenotype is now determined
by DNA-based techniques.
Methods: Here, we report a rapid optimized method which employs HRMA for
ACP1 polymorphism identification, a molecular approach that we used to
screen 80 healthy Italian subjects.
Results: HRMA proved particularly suitable for detecting ACP1 genotypes.
In fact, HRMA results were 100\% concordant with direct sequencing. In
addition, ACP1 genotype frequency in the Italian population was in
accordance with the literature {[4\% (*A/A), 36\% (*A/B), 4\%
(*A/C), 50\% (*B/B), 6\% (*B/C)].
Conclusions: HRMA was found to be a simple, rapid, sensitive and low
cost method potentially useful in research and diagnostic laboratories.
Finally, use of small amplicons for the set-up allowed us a better
optimization of HRMA. For this reason, we present such an approach as
small amplicons high resolution melting analysis (SA-HRMA). Finally,
ACP1 genotype frequency in the Italian population reported in this study
may contribute to a better interpretation of ACP1 allelic frequency
variation. (c) 2012 Elsevier B.V. All rights reserved.}
| Original language | English |
|---|---|
| Pages (from-to) | 86-91 |
| Number of pages | 6 |
| Journal | Clinica Chimica Acta |
| Volume | 416 |
| DOIs | |
| Publication status | Published - 2013 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- GENETIC-POLYMORPHISM
- PROTEIN-TYROSINE-PHOSPHATASE
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