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T Oligo-Primed Polymerase Chain Reaction (TOP-PCR): A Robust Method for the Amplification of Minute DNA Fragments in Body Fluids
Body fluid DNA sequencing is a powerful noninvasive approach for the diagnosis of genetic defects, infectious agents and diseases. The success relies on the quantity and quality of the DNA samples. However, numerous clinical samples are either at low quantity or of poor quality due to various reason...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240146/ https://www.ncbi.nlm.nih.gov/pubmed/28094343 http://dx.doi.org/10.1038/srep40767 |
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author | Nai, Yu-Shin Chen, Tzu-Han Huang, Yu-Feng Midha, Mohit K. Shiau, Hsin-Chieh Shen, Chen-Yang Chen, Chien-Jen Yu, Alice L. Chiu, Kuo Ping |
author_facet | Nai, Yu-Shin Chen, Tzu-Han Huang, Yu-Feng Midha, Mohit K. Shiau, Hsin-Chieh Shen, Chen-Yang Chen, Chien-Jen Yu, Alice L. Chiu, Kuo Ping |
author_sort | Nai, Yu-Shin |
collection | PubMed |
description | Body fluid DNA sequencing is a powerful noninvasive approach for the diagnosis of genetic defects, infectious agents and diseases. The success relies on the quantity and quality of the DNA samples. However, numerous clinical samples are either at low quantity or of poor quality due to various reasons. To overcome these problems, we have developed T oligo-primed polymerase chain reaction (TOP-PCR) for full-length nonselective amplification of minute quantity of DNA fragments. TOP-PCR adopts homogeneous “half adaptor” (HA), generated by annealing P oligo (carrying a phosphate group at the 5′ end) and T oligo (carrying a T-tail at the 3′ end), for efficient ligation to target DNA and subsequent PCR amplification primed by the T oligo alone. Using DNA samples from body fluids, we demonstrate that TOP-PCR recovers minute DNA fragments and maintains the DNA size profile, while enhancing the major molecular populations. Our results also showed that TOP-PCR is a superior method for detecting apoptosis and outperforms the method adopted by Illumina for DNA amplification. |
format | Online Article Text |
id | pubmed-5240146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52401462017-01-23 T Oligo-Primed Polymerase Chain Reaction (TOP-PCR): A Robust Method for the Amplification of Minute DNA Fragments in Body Fluids Nai, Yu-Shin Chen, Tzu-Han Huang, Yu-Feng Midha, Mohit K. Shiau, Hsin-Chieh Shen, Chen-Yang Chen, Chien-Jen Yu, Alice L. Chiu, Kuo Ping Sci Rep Article Body fluid DNA sequencing is a powerful noninvasive approach for the diagnosis of genetic defects, infectious agents and diseases. The success relies on the quantity and quality of the DNA samples. However, numerous clinical samples are either at low quantity or of poor quality due to various reasons. To overcome these problems, we have developed T oligo-primed polymerase chain reaction (TOP-PCR) for full-length nonselective amplification of minute quantity of DNA fragments. TOP-PCR adopts homogeneous “half adaptor” (HA), generated by annealing P oligo (carrying a phosphate group at the 5′ end) and T oligo (carrying a T-tail at the 3′ end), for efficient ligation to target DNA and subsequent PCR amplification primed by the T oligo alone. Using DNA samples from body fluids, we demonstrate that TOP-PCR recovers minute DNA fragments and maintains the DNA size profile, while enhancing the major molecular populations. Our results also showed that TOP-PCR is a superior method for detecting apoptosis and outperforms the method adopted by Illumina for DNA amplification. Nature Publishing Group 2017-01-17 /pmc/articles/PMC5240146/ /pubmed/28094343 http://dx.doi.org/10.1038/srep40767 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Nai, Yu-Shin Chen, Tzu-Han Huang, Yu-Feng Midha, Mohit K. Shiau, Hsin-Chieh Shen, Chen-Yang Chen, Chien-Jen Yu, Alice L. Chiu, Kuo Ping T Oligo-Primed Polymerase Chain Reaction (TOP-PCR): A Robust Method for the Amplification of Minute DNA Fragments in Body Fluids |
title | T Oligo-Primed Polymerase Chain Reaction (TOP-PCR): A Robust Method for the Amplification of Minute DNA Fragments in Body Fluids |
title_full | T Oligo-Primed Polymerase Chain Reaction (TOP-PCR): A Robust Method for the Amplification of Minute DNA Fragments in Body Fluids |
title_fullStr | T Oligo-Primed Polymerase Chain Reaction (TOP-PCR): A Robust Method for the Amplification of Minute DNA Fragments in Body Fluids |
title_full_unstemmed | T Oligo-Primed Polymerase Chain Reaction (TOP-PCR): A Robust Method for the Amplification of Minute DNA Fragments in Body Fluids |
title_short | T Oligo-Primed Polymerase Chain Reaction (TOP-PCR): A Robust Method for the Amplification of Minute DNA Fragments in Body Fluids |
title_sort | t oligo-primed polymerase chain reaction (top-pcr): a robust method for the amplification of minute dna fragments in body fluids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240146/ https://www.ncbi.nlm.nih.gov/pubmed/28094343 http://dx.doi.org/10.1038/srep40767 |
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