# Long-read plasmid sequencing strategy for evaluating intrinsic instability of tandem gene arrays

**Authors:** Hiroaki Takesue, Satoshi Okada, Takashi Ito

PMC · DOI: 10.17912/micropub.biology.001582 · microPublication Biology · 2025-05-08

## TL;DR

The paper introduces a sequencing method to study how unstable gene arrays are in yeast by measuring their length changes using long-read sequencing.

## Contribution

A novel nanopore sequencing strategy is proposed to evaluate the intrinsic instability of tandem gene arrays in yeast.

## Key findings

- Nanopore sequencing can directly determine the length distribution of gene arrays on plasmids.
- The method allows assessment of array instability and identification of factors influencing stability.

## Abstract

Tandem gene arrays are inherently unstable, particularly in recombination-prone organisms such as the budding yeast
Saccharomyces cerevisiae
. However, understanding the nature of this instability—how frequently and to what extent the target array contracts or expands within the genome—remains challenging. As a surrogate approach to this goal, we propose using nanopore long-read sequencing to directly determine the length distribution of a target gene array cloned onto a centromeric plasmid functioning as an artificial chromosome. This strategy will not only allow us to assess the intrinsic instability of the array but also help identify factors that may influence its stability.

## Linked entities

- **Species:** Saccharomyces cerevisiae (taxon 4932)

## Full-text entities

- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12100151/full.md

## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12100151/full.md

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Source: https://tomesphere.com/paper/PMC12100151