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Comparison of paired cerebrospinal fluid and serum cell‐free mitochondrial and nuclear DNA with copy number and fragment length
BACKGROUND: Most studies on cell‐free DNA (cfDNA) were only for single body fluids; however, the differences in cfDNA distribution between two body fluids are rarely reported. Hence, in this work, we compared the differences in cfDNA distribution between cerebrospinal fluid (CSF) and serum of patien...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307366/ https://www.ncbi.nlm.nih.gov/pubmed/32052892 http://dx.doi.org/10.1002/jcla.23238 |
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author | Chen, Aolong Li, Jun Wang, Lei Huang, Qin Zhu, Jiajin Wen, Shumeng Lyu, Jianxin Wu, Wenhe |
author_facet | Chen, Aolong Li, Jun Wang, Lei Huang, Qin Zhu, Jiajin Wen, Shumeng Lyu, Jianxin Wu, Wenhe |
author_sort | Chen, Aolong |
collection | PubMed |
description | BACKGROUND: Most studies on cell‐free DNA (cfDNA) were only for single body fluids; however, the differences in cfDNA distribution between two body fluids are rarely reported. Hence, in this work, we compared the differences in cfDNA distribution between cerebrospinal fluid (CSF) and serum of patients with brain‐related diseases. METHODS: The fragment length of cfDNA was determined by using Agilent 2100 Bioanalyzer. The copy numbers of cell‐free mitochondrial DNA (cf‐mtDNA) and cell‐free nuclear DNA (cf‐nDNA) were determined by using real‐time quantitative PCR (qPCR) and droplet digital PCR (ddPCR) with three pairs of mitochondrial ND1 and nuclear GAPDH primers, respectively. RESULTS: There were short (~60 bp), medium (~167 bp), and long (>250 bp) cfDNA fragment length distributions totally obtained from CSF and serum using Agilent 2100 Bioanalyzer. The results of both qPCR and ddPCR confirmed the existence of these three cfDNA fragment ranges in CSF and serum. According to qPCR, the copy numbers of long cf‐mtDNA, medium, and long cf‐nDNA in CSF were significantly higher than in paired serum. In CSF, only long cf‐mtDNA's copy numbers were higher than long cf‐nDNA. But in serum, the copy numbers of medium and long cf‐mtDNA were higher than the corresponding cf‐nDNA. CONCLUSION: The cf‐nDNA and cf‐mtDNA with different fragment lengths differentially distributed in the CSF and serum of patients with brain disorders, which might serve as a biomarker of human brain diseases. |
format | Online Article Text |
id | pubmed-7307366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73073662020-06-23 Comparison of paired cerebrospinal fluid and serum cell‐free mitochondrial and nuclear DNA with copy number and fragment length Chen, Aolong Li, Jun Wang, Lei Huang, Qin Zhu, Jiajin Wen, Shumeng Lyu, Jianxin Wu, Wenhe J Clin Lab Anal Research Articles BACKGROUND: Most studies on cell‐free DNA (cfDNA) were only for single body fluids; however, the differences in cfDNA distribution between two body fluids are rarely reported. Hence, in this work, we compared the differences in cfDNA distribution between cerebrospinal fluid (CSF) and serum of patients with brain‐related diseases. METHODS: The fragment length of cfDNA was determined by using Agilent 2100 Bioanalyzer. The copy numbers of cell‐free mitochondrial DNA (cf‐mtDNA) and cell‐free nuclear DNA (cf‐nDNA) were determined by using real‐time quantitative PCR (qPCR) and droplet digital PCR (ddPCR) with three pairs of mitochondrial ND1 and nuclear GAPDH primers, respectively. RESULTS: There were short (~60 bp), medium (~167 bp), and long (>250 bp) cfDNA fragment length distributions totally obtained from CSF and serum using Agilent 2100 Bioanalyzer. The results of both qPCR and ddPCR confirmed the existence of these three cfDNA fragment ranges in CSF and serum. According to qPCR, the copy numbers of long cf‐mtDNA, medium, and long cf‐nDNA in CSF were significantly higher than in paired serum. In CSF, only long cf‐mtDNA's copy numbers were higher than long cf‐nDNA. But in serum, the copy numbers of medium and long cf‐mtDNA were higher than the corresponding cf‐nDNA. CONCLUSION: The cf‐nDNA and cf‐mtDNA with different fragment lengths differentially distributed in the CSF and serum of patients with brain disorders, which might serve as a biomarker of human brain diseases. John Wiley and Sons Inc. 2020-02-13 /pmc/articles/PMC7307366/ /pubmed/32052892 http://dx.doi.org/10.1002/jcla.23238 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Chen, Aolong Li, Jun Wang, Lei Huang, Qin Zhu, Jiajin Wen, Shumeng Lyu, Jianxin Wu, Wenhe Comparison of paired cerebrospinal fluid and serum cell‐free mitochondrial and nuclear DNA with copy number and fragment length |
title | Comparison of paired cerebrospinal fluid and serum cell‐free mitochondrial and nuclear DNA with copy number and fragment length |
title_full | Comparison of paired cerebrospinal fluid and serum cell‐free mitochondrial and nuclear DNA with copy number and fragment length |
title_fullStr | Comparison of paired cerebrospinal fluid and serum cell‐free mitochondrial and nuclear DNA with copy number and fragment length |
title_full_unstemmed | Comparison of paired cerebrospinal fluid and serum cell‐free mitochondrial and nuclear DNA with copy number and fragment length |
title_short | Comparison of paired cerebrospinal fluid and serum cell‐free mitochondrial and nuclear DNA with copy number and fragment length |
title_sort | comparison of paired cerebrospinal fluid and serum cell‐free mitochondrial and nuclear dna with copy number and fragment length |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307366/ https://www.ncbi.nlm.nih.gov/pubmed/32052892 http://dx.doi.org/10.1002/jcla.23238 |
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