IDEAS home Printed from https://ideas.repec.org/a/gam/jijerp/v19y2022i13p8119-d854131.html
   My bibliography  Save this article

Resistance to Arsenite and Arsenate in Saccharomyces cerevisiae Arises through the Subtelomeric Expansion of a Cluster of Yeast Genes

Author

Listed:
  • Irene Stefanini

    (Department of Life Sciences and Systems Biology, University of Turin, 10123 Turin, Italy)

  • Monica Di Paola

    (Department of Biology, University of Florence, Sesto Fiorentino, 50019 Florence, Italy)

  • Gianni Liti

    (National Centre for Scientific Research (CNRS), National Institute of Health and Medical Research (INSERM), Institute for Research on Cancer and Aging (IRCAN), Université Côte d’Azur, 06103 Nice, France)

  • Andrea Marranci

    (Core Research Laboratory, Oncogenomics Unit, Istituto di Fisiologia Clinica, Institute for Cancer Research and Pre-vention (ISPRO), 56124 Pisa, Italy)

  • Federico Sebastiani

    (Institute for Sustainable Plant Protection, National Research Council (IPSP-CNR), Sesto Fiorentino, 50019 Florence, Italy)

  • Enrico Casalone

    (Department of Biology, University of Florence, Sesto Fiorentino, 50019 Florence, Italy)

  • Duccio Cavalieri

    (Department of Biology, University of Florence, Sesto Fiorentino, 50019 Florence, Italy)

Abstract

Arsenic is one of the most prevalent toxic elements in the environment, and its toxicity affects every organism. Arsenic resistance has mainly been observed in microorganisms, and, in bacteria, it has been associated with the presence of the Ars operon. In Saccharomyces cerevisiae , three genes confer arsenic resistance: ARR1 , ARR2 , and ARR3 . Unlike bacteria, in which the presence of the Ars genes confers per se resistance to arsenic, most of the S. cerevisiae isolates present the three ARR genes, regardless of whether the strain is resistant or sensitive to arsenic. To assess the genetic features that make natural S. cerevisiae strains resistant to arsenic, we used a combination of comparative genomic hybridization, whole-genome sequencing, and transcriptomics profiling with microarray analyses. We observed that both the presence and the genomic location of multiple copies of the whole cluster of ARR genes were central to the escape from subtelomeric silencing and the acquisition of resistance to arsenic. As a result of the repositioning, the ARR genes were expressed even in the absence of arsenic. In addition to their relevance in improving our understanding of the mechanism of arsenic resistance in yeast, these results provide evidence for a new cluster of functionally related genes that are independently duplicated and translocated.

Suggested Citation

  • Irene Stefanini & Monica Di Paola & Gianni Liti & Andrea Marranci & Federico Sebastiani & Enrico Casalone & Duccio Cavalieri, 2022. "Resistance to Arsenite and Arsenate in Saccharomyces cerevisiae Arises through the Subtelomeric Expansion of a Cluster of Yeast Genes," IJERPH, MDPI, vol. 19(13), pages 1-15, July.
  • Handle: RePEc:gam:jijerp:v:19:y:2022:i:13:p:8119-:d:854131
    as

    Download full text from publisher

    File URL: https://www.mdpi.com/1660-4601/19/13/8119/pdf
    Download Restriction: no

    File URL: https://www.mdpi.com/1660-4601/19/13/8119/
    Download Restriction: no
    ---><---

    References listed on IDEAS

    as
    1. Ravi K Patel & Mukesh Jain, 2012. "NGS QC Toolkit: A Toolkit for Quality Control of Next Generation Sequencing Data," PLOS ONE, Public Library of Science, vol. 7(2), pages 1-7, February.
    2. Simone Morais & Henrique M. A. C. Fonseca & Sónia M. R. Oliveira & Helena Oliveira & Vivek Kumar Gupta & Bechan Sharma & Maria de Lourdes Pereira, 2021. "Environmental and Health Hazards of Chromated Copper Arsenate-Treated Wood: A Review," IJERPH, MDPI, vol. 18(11), pages 1-12, May.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Dongya Wu & Enhui Shen & Bowen Jiang & Yu Feng & Wei Tang & Sangting Lao & Lei Jia & Han-Yang Lin & Lingjuan Xie & Xifang Weng & Chenfeng Dong & Qinghong Qian & Feng Lin & Haiming Xu & Huabing Lu & Lu, 2022. "Genomic insights into the evolution of Echinochloa species as weed and orphan crop," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    2. Abrar E Al-Shaer & George R Flentke & Mark E Berres & Ana Garic & Susan M Smith, 2019. "Exon level machine learning analyses elucidate novel candidate miRNA targets in an avian model of fetal alcohol spectrum disorder," PLOS Computational Biology, Public Library of Science, vol. 15(4), pages 1-25, April.
    3. Wei Ding & Shougang Wang & Peng Qin & Shen Fan & Xiaoyan Su & Peiyan Cai & Jie Lu & Han Cui & Meng Wang & Yi Shu & Yongming Wang & Hui-Hui Fu & Yu-Zhong Zhang & Yong-Xin Li & Weipeng Zhang, 2023. "Anaerobic thiosulfate oxidation by the Roseobacter group is prevalent in marine biofilms," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    4. Wenxiu Wang & Weizhi Song & Marwan E. Majzoub & Xiaoyuan Feng & Bu Xu & Jianchang Tao & Yuanqing Zhu & Zhiyong Li & Pei-Yuan Qian & Nicole S. Webster & Torsten Thomas & Lu Fan, 2024. "Decoupling of strain- and intrastrain-level interactions of microbiomes in a sponge holobiont," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    5. Lihong Gu & Feng Wang & Zhemin Lin & Tieshan Xu & Dajie Lin & Manping Xing & Shaoxiong Yang & Zhe Chao & Baoguo Ye & Peng Lin & Chunhui Hui & Lizhi Lu & Shuisheng Hou, 2020. "Genetic characteristics of Jiaji Duck by whole genome re-sequencing," PLOS ONE, Public Library of Science, vol. 15(2), pages 1-15, February.
    6. Pingfen Zhu & Weiqiang Liu & Xiaoxiao Zhang & Meng Li & Gaoming Liu & Yang Yu & Zihao Li & Xuanjing Li & Juan Du & Xiao Wang & Cyril C. Grueter & Ming Li & Xuming Zhou, 2023. "Correlated evolution of social organization and lifespan in mammals," Nature Communications, Nature, vol. 14(1), pages 1-18, December.

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jijerp:v:19:y:2022:i:13:p:8119-:d:854131. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager (email available below). General contact details of provider: https://www.mdpi.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.