Engineering gene overlaps to sustain genetic constructs in vivo
Evolution is often an obstacle to the engineering of stable biological systems due to the selection of mutations inactivating costly gene circuits. Gene overlaps induce important constraints on sequences and their evolution. We show that these constraints can be harnessed to increase the stability o...
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creator | Decrulle, Antoine L Frénoy, Antoine Meiller-Legrand, Thomas A Bernheim, Aude Lotton, Chantal Gutierrez, Arnaud Lindner, Ariel B |
description | Evolution is often an obstacle to the engineering of stable biological systems due to the selection of mutations inactivating costly gene circuits. Gene overlaps induce important constraints on sequences and their evolution. We show that these constraints can be harnessed to increase the stability of costly genes by purging loss-of-function mutations. We combine computational and synthetic biology approaches to rationally design an overlapping reading frame expressing an essential gene within an existing gene to protect. Our algorithm succeeded in creating overlapping reading frames in 80% of E. coli genes. Experimentally, scoring mutations in both genes of such overlapping construct, we found that a significant fraction of mutations impacting the gene to protect have a deleterious effect on the essential gene. Such an overlap thus protects a costly gene from removal by natural selection by associating the benefit of this removal with a larger or even lethal cost. In our synthetic constructs, the overlap converts many of the possible mutants into evolutionary dead-ends, reducing the evolutionary potential of the system and thus increasing its stability over time. |
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Gene overlaps induce important constraints on sequences and their evolution. We show that these constraints can be harnessed to increase the stability of costly genes by purging loss-of-function mutations. We combine computational and synthetic biology approaches to rationally design an overlapping reading frame expressing an essential gene within an existing gene to protect. Our algorithm succeeded in creating overlapping reading frames in 80% of E. coli genes. Experimentally, scoring mutations in both genes of such overlapping construct, we found that a significant fraction of mutations impacting the gene to protect have a deleterious effect on the essential gene. Such an overlap thus protects a costly gene from removal by natural selection by associating the benefit of this removal with a larger or even lethal cost. In our synthetic constructs, the overlap converts many of the possible mutants into evolutionary dead-ends, reducing the evolutionary potential of the system and thus increasing its stability over time.</description><identifier>ISSN: 1553-7358</identifier><identifier>ISSN: 1553-734X</identifier><identifier>EISSN: 1553-7358</identifier><identifier>DOI: 10.1371/journal.pcbi.1009475</identifier><identifier>PMID: 34624014</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Algorithms ; Amino acids ; Analysis ; Binding sites ; Biological evolution ; Biology and Life Sciences ; Cloning ; Computational biology ; Computer applications ; Computer engineering ; Confidence intervals ; E coli ; Engineering and Technology ; Escherichia coli ; Escherichia coli - genetics ; Evolution ; Evolution, Molecular ; Genes ; Genes, Essential - genetics ; Genetic aspects ; Genetic engineering ; Genetic Engineering - methods ; Genomes ; Genomics ; Identification and classification ; Life Sciences ; Methods ; Mutation ; Mutation - genetics ; Natural selection ; Organisms ; Proteins ; Purging ; Reading ; Reading Frames - genetics ; Research and Analysis Methods ; Sequence Analysis, DNA ; Stability ; Synthetic biology ; Synthetic Biology - methods ; Values</subject><ispartof>PLoS computational biology, 2021-10, Vol.17 (10), p.e1009475-e1009475</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Decrulle et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2021 Decrulle et al 2021 Decrulle et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c695t-faf71b669b807ae2265ac4f088b2bcde88931eae30047903e6f1eafcd5d8f1fc3</citedby><cites>FETCH-LOGICAL-c695t-faf71b669b807ae2265ac4f088b2bcde88931eae30047903e6f1eafcd5d8f1fc3</cites><orcidid>0000-0002-3539-8915 ; 0000-0001-6472-2991 ; 0000-0003-0212-777X ; 0000-0002-9512-0659</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528312/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528312/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2919,23857,27915,27916,53782,53784,79361,79362</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34624014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03800488$$DView record in HAL$$Hfree_for_read</backlink></links><search><contributor>Braun, Edward L.</contributor><creatorcontrib>Decrulle, Antoine L</creatorcontrib><creatorcontrib>Frénoy, Antoine</creatorcontrib><creatorcontrib>Meiller-Legrand, Thomas A</creatorcontrib><creatorcontrib>Bernheim, Aude</creatorcontrib><creatorcontrib>Lotton, Chantal</creatorcontrib><creatorcontrib>Gutierrez, Arnaud</creatorcontrib><creatorcontrib>Lindner, Ariel B</creatorcontrib><title>Engineering gene overlaps to sustain genetic constructs in vivo</title><title>PLoS computational biology</title><addtitle>PLoS Comput Biol</addtitle><description>Evolution is often an obstacle to the engineering of stable biological systems due to the selection of mutations inactivating costly gene circuits. Gene overlaps induce important constraints on sequences and their evolution. We show that these constraints can be harnessed to increase the stability of costly genes by purging loss-of-function mutations. We combine computational and synthetic biology approaches to rationally design an overlapping reading frame expressing an essential gene within an existing gene to protect. Our algorithm succeeded in creating overlapping reading frames in 80% of E. coli genes. Experimentally, scoring mutations in both genes of such overlapping construct, we found that a significant fraction of mutations impacting the gene to protect have a deleterious effect on the essential gene. Such an overlap thus protects a costly gene from removal by natural selection by associating the benefit of this removal with a larger or even lethal cost. 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Gene overlaps induce important constraints on sequences and their evolution. We show that these constraints can be harnessed to increase the stability of costly genes by purging loss-of-function mutations. We combine computational and synthetic biology approaches to rationally design an overlapping reading frame expressing an essential gene within an existing gene to protect. Our algorithm succeeded in creating overlapping reading frames in 80% of E. coli genes. Experimentally, scoring mutations in both genes of such overlapping construct, we found that a significant fraction of mutations impacting the gene to protect have a deleterious effect on the essential gene. Such an overlap thus protects a costly gene from removal by natural selection by associating the benefit of this removal with a larger or even lethal cost. In our synthetic constructs, the overlap converts many of the possible mutants into evolutionary dead-ends, reducing the evolutionary potential of the system and thus increasing its stability over time.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>34624014</pmid><doi>10.1371/journal.pcbi.1009475</doi><orcidid>https://orcid.org/0000-0002-3539-8915</orcidid><orcidid>https://orcid.org/0000-0001-6472-2991</orcidid><orcidid>https://orcid.org/0000-0003-0212-777X</orcidid><orcidid>https://orcid.org/0000-0002-9512-0659</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Amino acids Analysis Binding sites Biological evolution Biology and Life Sciences Cloning Computational biology Computer applications Computer engineering Confidence intervals E coli Engineering and Technology Escherichia coli Escherichia coli - genetics Evolution Evolution, Molecular Genes Genes, Essential - genetics Genetic aspects Genetic engineering Genetic Engineering - methods Genomes Genomics Identification and classification Life Sciences Methods Mutation Mutation - genetics Natural selection Organisms Proteins Purging Reading Reading Frames - genetics Research and Analysis Methods Sequence Analysis, DNA Stability Synthetic biology Synthetic Biology - methods Values |
title | Engineering gene overlaps to sustain genetic constructs in vivo |
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