Novel insights into the effects of 5-hydroxymethfurural on genomic instability and phenotypic evolution using a yeast

Ying-Xuan Zhu1,2, Min He1, Ke-Jing Li2

  • 1Hainan Institute of Zhejiang University, Zhejiang University, Sanya, China.

Insights

5-Hydroxymethfurural (5-HMF) increases genomic instability in yeast, causing aneuploidy and mutations. However, this chromosomal instability can enhance yeast tolerance to 5-HMF, aiding environmental adaptation.

Area of Science:

  • Microbiology
  • Genetics
  • Biochemistry

Background:

  • 5-Hydroxymethfurural (5-HMF) is a common food and lignocellulosic hydrolysate inhibitor.
  • Yeast, such as *Saccharomyces cerevisiae*, face various stressors in industrial and natural environments.

Purpose of the Study:

  • To investigate the impact of 5-HMF on the genomic stability and phenotypic plasticity of *Saccharomyces cerevisiae*.
  • To understand the mechanisms of 5-HMF-induced genomic alterations and their role in yeast adaptation.

Main Methods:

  • Utilized next-generation sequencing to analyze genomic alterations in yeast subcultured on 5-HMF-containing media.
  • Examined rates of chromosome aneuploidy, large deletions/duplications, loss of heterozygosity, and point mutations.
  • Investigated the effect of specific gene overexpression (*ADH6*, *ZWF1*) on genomic stability.

Main Results:

  • 5-HMF exposure elevated rates of aneuploidy, large deletions/duplications, and loss of heterozygosity.
  • A shift in mutation spectrum and a higher incidence of monosomy over trisomy were observed.
  • A monosomic mutant (chromosome IX) exhibited increased resistance to 5-HMF due to enhanced alcohol dehydrogenase activity.
  • Overexpression of *ADH6* and *ZWF1* stabilized the yeast genome under 5-HMF stress.

Conclusions:

  • 5-HMF significantly impacts yeast genomic integrity, driving chromosomal instability.
  • Chromosomal loss, often detrimental, can confer tolerance to stressors like 5-HMF, facilitating environmental adaptation.
  • Findings provide insights into stress-induced genomic plasticity and eukaryotic cell adaptation.