Cargando…
Isolation and analysis of high quality nuclear DNA with reduced organellar DNA for plant genome sequencing and resequencing
BACKGROUND: High throughput sequencing (HTS) technologies have revolutionized the field of genomics by drastically reducing the cost of sequencing, making it feasible for individual labs to sequence or resequence plant genomes. Obtaining high quality, high molecular weight DNA from plants poses sign...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131251/ https://www.ncbi.nlm.nih.gov/pubmed/21599914 http://dx.doi.org/10.1186/1472-6750-11-54 |
_version_ | 1782207702262349824 |
---|---|
author | Lutz, Kerry A Wang, Wenqin Zdepski, Anna Michael, Todd P |
author_facet | Lutz, Kerry A Wang, Wenqin Zdepski, Anna Michael, Todd P |
author_sort | Lutz, Kerry A |
collection | PubMed |
description | BACKGROUND: High throughput sequencing (HTS) technologies have revolutionized the field of genomics by drastically reducing the cost of sequencing, making it feasible for individual labs to sequence or resequence plant genomes. Obtaining high quality, high molecular weight DNA from plants poses significant challenges due to the high copy number of chloroplast and mitochondrial DNA, as well as high levels of phenolic compounds and polysaccharides. Multiple methods have been used to isolate DNA from plants; the CTAB method is commonly used to isolate total cellular DNA from plants that contain nuclear DNA, as well as chloroplast and mitochondrial DNA. Alternatively, DNA can be isolated from nuclei to minimize chloroplast and mitochondrial DNA contamination. RESULTS: We describe optimized protocols for isolation of nuclear DNA from eight different plant species encompassing both monocot and eudicot species. These protocols use nuclei isolation to minimize chloroplast and mitochondrial DNA contamination. We also developed a protocol to determine the number of chloroplast and mitochondrial DNA copies relative to the nuclear DNA using quantitative real time PCR (qPCR). We compared DNA isolated from nuclei to total cellular DNA isolated with the CTAB method. As expected, DNA isolated from nuclei consistently yielded nuclear DNA with fewer chloroplast and mitochondrial DNA copies, as compared to the total cellular DNA prepared with the CTAB method. This protocol will allow for analysis of the quality and quantity of nuclear DNA before starting a plant whole genome sequencing or resequencing experiment. CONCLUSIONS: Extracting high quality, high molecular weight nuclear DNA in plants has the potential to be a bottleneck in the era of whole genome sequencing and resequencing. The methods that are described here provide a framework for researchers to extract and quantify nuclear DNA in multiple types of plants. |
format | Online Article Text |
id | pubmed-3131251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31312512011-07-08 Isolation and analysis of high quality nuclear DNA with reduced organellar DNA for plant genome sequencing and resequencing Lutz, Kerry A Wang, Wenqin Zdepski, Anna Michael, Todd P BMC Biotechnol Methodology Article BACKGROUND: High throughput sequencing (HTS) technologies have revolutionized the field of genomics by drastically reducing the cost of sequencing, making it feasible for individual labs to sequence or resequence plant genomes. Obtaining high quality, high molecular weight DNA from plants poses significant challenges due to the high copy number of chloroplast and mitochondrial DNA, as well as high levels of phenolic compounds and polysaccharides. Multiple methods have been used to isolate DNA from plants; the CTAB method is commonly used to isolate total cellular DNA from plants that contain nuclear DNA, as well as chloroplast and mitochondrial DNA. Alternatively, DNA can be isolated from nuclei to minimize chloroplast and mitochondrial DNA contamination. RESULTS: We describe optimized protocols for isolation of nuclear DNA from eight different plant species encompassing both monocot and eudicot species. These protocols use nuclei isolation to minimize chloroplast and mitochondrial DNA contamination. We also developed a protocol to determine the number of chloroplast and mitochondrial DNA copies relative to the nuclear DNA using quantitative real time PCR (qPCR). We compared DNA isolated from nuclei to total cellular DNA isolated with the CTAB method. As expected, DNA isolated from nuclei consistently yielded nuclear DNA with fewer chloroplast and mitochondrial DNA copies, as compared to the total cellular DNA prepared with the CTAB method. This protocol will allow for analysis of the quality and quantity of nuclear DNA before starting a plant whole genome sequencing or resequencing experiment. CONCLUSIONS: Extracting high quality, high molecular weight nuclear DNA in plants has the potential to be a bottleneck in the era of whole genome sequencing and resequencing. The methods that are described here provide a framework for researchers to extract and quantify nuclear DNA in multiple types of plants. BioMed Central 2011-05-20 /pmc/articles/PMC3131251/ /pubmed/21599914 http://dx.doi.org/10.1186/1472-6750-11-54 Text en Copyright ©2011 Lutz et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Lutz, Kerry A Wang, Wenqin Zdepski, Anna Michael, Todd P Isolation and analysis of high quality nuclear DNA with reduced organellar DNA for plant genome sequencing and resequencing |
title | Isolation and analysis of high quality nuclear DNA with reduced organellar DNA for plant genome sequencing and resequencing |
title_full | Isolation and analysis of high quality nuclear DNA with reduced organellar DNA for plant genome sequencing and resequencing |
title_fullStr | Isolation and analysis of high quality nuclear DNA with reduced organellar DNA for plant genome sequencing and resequencing |
title_full_unstemmed | Isolation and analysis of high quality nuclear DNA with reduced organellar DNA for plant genome sequencing and resequencing |
title_short | Isolation and analysis of high quality nuclear DNA with reduced organellar DNA for plant genome sequencing and resequencing |
title_sort | isolation and analysis of high quality nuclear dna with reduced organellar dna for plant genome sequencing and resequencing |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131251/ https://www.ncbi.nlm.nih.gov/pubmed/21599914 http://dx.doi.org/10.1186/1472-6750-11-54 |
work_keys_str_mv | AT lutzkerrya isolationandanalysisofhighqualitynucleardnawithreducedorganellardnaforplantgenomesequencingandresequencing AT wangwenqin isolationandanalysisofhighqualitynucleardnawithreducedorganellardnaforplantgenomesequencingandresequencing AT zdepskianna isolationandanalysisofhighqualitynucleardnawithreducedorganellardnaforplantgenomesequencingandresequencing AT michaeltoddp isolationandanalysisofhighqualitynucleardnawithreducedorganellardnaforplantgenomesequencingandresequencing |