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15.2:

Aislamiento del ADN

JoVE Core
Molecular Biology
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JoVE Core Molecular Biology
DNA Isolation

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DNA needs to be isolated from cells and cut at precise positions for many applications, such as recombinant DNA technology. Though different types of DNA extraction methods are used for different cell types, there are three standard steps: cell lysis, protein removal, and DNA recovery. Inside eukaryotic cells, DNA is packed within the nucleus. Thus, both the cell membrane and the nuclear membrane need to be ruptured to isolate the DNA. This step can be done mechanically by breaking down cells through grinding or sonication, or chemically by using detergents and enzymes to dissolve parts of the cell membrane. Once the cell contents are released, the debris is separated from soluble components by centrifugation. The supernatant recovered contains nucleic acids and water-soluble proteins. To remove proteins, enzymes, such as proteinase K, peptidase, or lysozyme, are added to the supernatant to break the peptide bonds. DNA is recovered from the supernatant through precipitation by adding alcohol and a salt, such as sodium acetate. The isolated precipitate is dissolved in water or a buffer.

15.2:

Aislamiento del ADN

DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow specific protocols even for genomic DNA extraction.

Types of genomic DNA extraction methods

The main aim of genomic DNA extraction methods is to separate gDNA from proteins, RNA, and other cell content. It involves four basic steps – 1. Disruption of the cell structure mechanically or using chemicals to obtain the cell lysate 2. Protection of DNA from degradation during processing 3. Separation of the soluble DNA from cell debris 4. Elution of purified DNA.

Most genomic DNA isolation protocols are either solution-based or solid-phase extraction methods. Solution-based methods rely on precipitation and centrifugation steps to separate DNA from other cellular material, followed by organic extraction or "salting out" to separate soluble DNA from cellular proteins. The final DNA precipitation is done using ethanol. In contrast, solid-phase extraction methods use solid support, such as silica or cellulose matrices, to bind DNA, followed by washing and DNA elution from the solid support. It involves centrifugation, vacuum, or magnetic methods to separate the bound DNA from other cellular components.

The choice of gDNA extraction method depends on the type of sample, the number of samples to be processed at once, and the downstream application of the DNA.

Suggested Reading

  1. Goldenberger, Daniel, Inge Perschil, Michael Ritzler, and Martin Altwegg. "A simple" universal" DNA extraction procedure using SDS and proteinase K is compatible with direct PCR amplification." Genome Research 4, no. 6 (1995): 368-370.
  2. Bimboim, H. C., and Janine Doly. "A rapid alkaline extraction procedure for screening recombinant plasmid DNA." Nucleic acids research 7, no. 6 (1979): 1513-1523.
  3. Oakes, Christopher C., Sophie La Salle, Jacquetta M. Trasler, and Bernard Robaire. "Restriction digestion and real-time PCR (qAMP)." In DNA Methylation, pp. 271-280. Humana Press, 2009.