Extracellular Self-DNA Effects on Yeast Cell Cycle and Transcriptome during Batch Growth

Author:

Palomba Emanuela1,Chiusano Maria Luisa2ORCID,Monticolo Francesco23,Langella Maria Chiara2,Sanchez Massimo4,Tirelli Valentina4,de Alteriis Elisabetta5ORCID,Iannaccone Marco6,Termolino Pasquale1ORCID,Capparelli Rosanna2,Carteni Fabrizio2ORCID,Incerti Guido7ORCID,Mazzoleni Stefano2ORCID

Affiliation:

1. Institute of Biosciences and Bioresources CNR, Via Università 133, 80055 Portici, Italy

2. Department of Agricultural Sciences, University of Naples “Federico II”, Via Università 100, 80055 Portici, Italy

3. Cutaneous Biology Research Center, Massachusetts General Hospital, Boston, MA 02129, USA

4. Istituto Superiore di Sanità (ISS) Core Facilities, Viale Regina Elena 299, 00161 Rome, Italy

5. Department of Biology, University of Naples “Federico II”, Via Cinthia 26, 80126 Naples, Italy

6. Laboratory of Bioproducts and Bioprocesses ENEA, Piazzale Enrico Fermi 1, 80055 Portici, Italy

7. Department of Agricultural, Food, Environmental and Animal Sciences, University of Udine, Via delle Scienze 206, 33100 Udine, Italy

Abstract

The cell cycle and the transcriptome dynamics of yeast exposed to extracellular self-DNA during an aerobic batch culture on glucose have been investigated using cytofluorimetric and RNA-seq analyses. In parallel, the same study was conducted on yeast cells growing in the presence of (heterologous) nonself-DNA. The self-DNA treatment determined a reduction in the growth rate and a major elongation of the diauxic lag phase, as well as a significant delay in the achievement of the stationary phase. This was associated with significant changes in the cell cycle dynamics, with slower exit from the G0 phase, followed by an increased level of cell percentage in the S phase, during the cultivation. Comparatively, the exposure to heterologous DNA did not affect the growth curve and the cell cycle dynamics. The transcriptomic analysis showed that self-DNA exposure produced a generalized downregulation of transmembrane transport and an upregulation of genes associated with sulfur compounds and the pentose phosphate pathway. Instead, in the case of the nonself treatment, a clear response to nutrient deprivation was detected. Overall, the presented findings represent further insights into the complex functional mechanisms of self-DNA inhibition.

Publisher

MDPI AG

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