# Efficient DNA extraction from cytogenetic suspensions: A new possibility for obtaining DNA, with potential applications in studies of molecular markers

**Authors:** Geórgia Liz Monteiro Sant’ana-Arruda, Paulo Cesar Venere, Daniela Cristina Ferreira

PMC · DOI: 10.1371/journal.pone.0335898 · 2025-11-07

## TL;DR

This study shows that high-quality DNA can be extracted from old fish cell suspensions, enabling molecular studies even when fresh samples are unavailable.

## Contribution

A new DNA extraction method is introduced, using long-stored cytogenetic samples to obtain high-quality genomic DNA.

## Key findings

- DNA extracted from 27 fish specimens showed high purity and concentration.
- PCR successfully amplified four genes, including efficient sequencing of COI.
- The method allows for retrospective molecular studies using archived samples.

## Abstract

The present study demonstrates the viability of extracting DNA for genomic analyses from cell suspensions prepared for cytogenetic analyses, specifically, samples fixed in Carnoy’s solution (3:1 methanol: acetic acid) and stored at –20 °C for more than 10 years. Cell suspensions from 27 specimens of fish of the subfamily Loricariinae, which had been prepared originally for cytogenetic studies, were used to test a DNA extraction procedure based on a routinely-used protocol with specific minor adjustments. The spectrophotometric and electrophoretic analyses of the extracted samples revealed DNA at good concentrations (5.9–1739 ng.μL-1) and high purity (A260/A280 ratios of 1.75–2.07), indicating negligible contamination and no significant fragmentation. The integrity of the material was confirmed by the successful amplification by PCR of four different genes (COI, 5S, 18S, and RAG2), with the COI gene being sequenced efficiently. These results demonstrate that DNA can be extracted from samples collected for other purposes, even after long-term storage, producing high-quality genomic DNA from sources that might otherwise be overlooked. The exploitation of these samples as a source of DNA represents a useful potential strategy for the acquisition of material for analysis when fresh samples are scarce or difficult to obtain. This novel approach expands considerably the possibilities for retrospective molecular studies, especially in the fields of conservation and systematics.

## Linked entities

- **Genes:** COX1 (cytochrome c oxidase subunit I) [NCBI Gene 4512], 5S (5S ribosomal RNA) [NCBI Gene 10446500], RAG2 (recombination activating 2) [NCBI Gene 5897]
- **Chemicals:** methanol (PubChem CID 887), acetic acid (PubChem CID 176)
- **Species:** Loricariinae (taxon 503143)

## Full-text entities

- **Genes:** COX1 (cytochrome c oxidase subunit I) [NCBI Gene 4512] {aka COI, MTCO1}, RAG2 (recombination activating 2) [NCBI Gene 5897] {aka RAG-2}
- **Chemicals:** acetic acid (MESH:D019342), methanol (MESH:D000432), Carnoy's solution (MESH:C033474)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12594425/full.md

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Source: https://tomesphere.com/paper/PMC12594425