Gene gain by horizontal gene transfer is a major pathway of genome innovation in bacteria. The current view posits that acquired genes initially need to be silenced and that a bacterial chromatin protein, H-NS, plays a role in this silencing. However, we lack direct observation of the early fate of a horizontally transferred gene to prove this theory. We combine sequencing, flow cytometry and sorting, followed by microscopy to monitor gene expression and its variability after large-scale random insertions of a reporter gene in a population of Escherichia coli bacteria. We find that inserted promoters have a wide range of gene-expression variability related to their location. We find that high-expression clones carry insertions that are not correlated with H-NS binding. Conversely, binding of H-NS correlates with silencing. Finally, while most promoters show a common level of extrinsic noise, some insertions show higher noise levels. Analysis of these high-noise clones supports a scenario of switching due to transcriptional interference from divergent ribosomal promoters. Altogether, our findings point to evolutionary pathways where newly-acquired genes are not necessarily silenced, but may immediately explore a wide range of expression levels to probe the optimal ones.

Early fate of exogenous promoters in E. coli / M. Yousuf, I. Iuliani, R.T. Veetil, A.S.N. Seshasayee, B. Sclavi, M. Cosentino Lagomarsino. - In: NUCLEIC ACIDS RESEARCH. - ISSN 0305-1048. - 48:5(2020 Mar), pp. 2348-2356. [10.1093/nar/gkz1196]

Early fate of exogenous promoters in E. coli

M. Cosentino Lagomarsino
Ultimo
2020

Abstract

Gene gain by horizontal gene transfer is a major pathway of genome innovation in bacteria. The current view posits that acquired genes initially need to be silenced and that a bacterial chromatin protein, H-NS, plays a role in this silencing. However, we lack direct observation of the early fate of a horizontally transferred gene to prove this theory. We combine sequencing, flow cytometry and sorting, followed by microscopy to monitor gene expression and its variability after large-scale random insertions of a reporter gene in a population of Escherichia coli bacteria. We find that inserted promoters have a wide range of gene-expression variability related to their location. We find that high-expression clones carry insertions that are not correlated with H-NS binding. Conversely, binding of H-NS correlates with silencing. Finally, while most promoters show a common level of extrinsic noise, some insertions show higher noise levels. Analysis of these high-noise clones supports a scenario of switching due to transcriptional interference from divergent ribosomal promoters. Altogether, our findings point to evolutionary pathways where newly-acquired genes are not necessarily silenced, but may immediately explore a wide range of expression levels to probe the optimal ones.
Chromatin; Escherichia coli; Escherichia coli Proteins; Fimbriae Proteins; Gene Dosage; Gene Silencing; Gene Transfer, Horizontal; Genes, Reporter; Green Fluorescent Proteins; Protein Binding; Protein Biosynthesis; Transgenes; Gene Expression Regulation, Bacterial; Mutagenesis, Insertional; Promoter Regions, Genetic
Settore FIS/02 - Fisica Teorica, Modelli e Metodi Matematici
Settore BIO/09 - Fisiologia
Settore BIO/11 - Biologia Molecolare
mar-2020
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/737827
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