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Telomere-to-Telomere genome assemblies of human-infecting Encephalitozoon species
Microsporidia are diverse spore forming, fungal-related obligate intracellular pathogens infecting a wide range of hosts. This diversity is reflected at the genome level with sizes varying by an order of magnitude, ranging from less than 3 Mb in Encephalitozoon species (the smallest known in eukaryo...
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Published in: | BMC genomics 2023-05, Vol.24 (1), p.237-19, Article 237 |
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description | Microsporidia are diverse spore forming, fungal-related obligate intracellular pathogens infecting a wide range of hosts. This diversity is reflected at the genome level with sizes varying by an order of magnitude, ranging from less than 3 Mb in Encephalitozoon species (the smallest known in eukaryotes) to more than 50 Mb in Edhazardia spp. As a paradigm of genome reduction in eukaryotes, the small Encephalitozoon genomes have attracted much attention with investigations revealing gene dense, repeat- and intron-poor genomes characterized by a thorough pruning of molecular functions no longer relevant to their obligate intracellular lifestyle. However, because no Encephalitozoon genome has been sequenced from telomere-to-telomere and since no methylation data is available for these species, our understanding of their overall genetic and epigenetic architectures is incomplete.
In this study, we sequenced the complete genomes from telomere-to-telomere of three human-infecting Encephalitozoon spp. -E. intestinalis ATCC 50506, E. hellem ATCC 50604 and E. cuniculi ATCC 50602- using short and long read platforms and leveraged the data generated as part of the sequencing process to investigate the presence of epigenetic markers in these genomes. We also used a mixture of sequence- and structure-based computational approaches, including protein structure prediction, to help identify which Encephalitozoon proteins are involved in telomere maintenance, epigenetic regulation, and heterochromatin formation.
The Encephalitozoon chromosomes were found capped by TTAGG 5-mer telomeric repeats followed by telomere associated repeat elements (TAREs) flanking hypermethylated ribosomal RNA (rRNA) gene loci featuring 5-methylcytosines (5mC) and 5-hemimethylcytosines (5hmC), themselves followed by lesser methylated subtelomeres and hypomethylated chromosome cores. Strong nucleotide biases were identified between the telomeres/subtelomeres and chromosome cores with significant changes in GC/AT, GT/AC and GA/CT contents. The presence of several genes coding for proteins essential to telomere maintenance, epigenetic regulation, and heterochromatin formation was further confirmed in the Encephalitozoon genomes.
Altogether, our results strongly support the subtelomeres as sites of heterochromatin formation in Encephalitozoon genomes and further suggest that these species might shutdown their energy-consuming ribosomal machinery while dormant as spores by silencing of the rRNA genes u |
doi_str_mv | 10.1186/s12864-023-09331-3 |
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In this study, we sequenced the complete genomes from telomere-to-telomere of three human-infecting Encephalitozoon spp. -E. intestinalis ATCC 50506, E. hellem ATCC 50604 and E. cuniculi ATCC 50602- using short and long read platforms and leveraged the data generated as part of the sequencing process to investigate the presence of epigenetic markers in these genomes. We also used a mixture of sequence- and structure-based computational approaches, including protein structure prediction, to help identify which Encephalitozoon proteins are involved in telomere maintenance, epigenetic regulation, and heterochromatin formation.
The Encephalitozoon chromosomes were found capped by TTAGG 5-mer telomeric repeats followed by telomere associated repeat elements (TAREs) flanking hypermethylated ribosomal RNA (rRNA) gene loci featuring 5-methylcytosines (5mC) and 5-hemimethylcytosines (5hmC), themselves followed by lesser methylated subtelomeres and hypomethylated chromosome cores. Strong nucleotide biases were identified between the telomeres/subtelomeres and chromosome cores with significant changes in GC/AT, GT/AC and GA/CT contents. The presence of several genes coding for proteins essential to telomere maintenance, epigenetic regulation, and heterochromatin formation was further confirmed in the Encephalitozoon genomes.
Altogether, our results strongly support the subtelomeres as sites of heterochromatin formation in Encephalitozoon genomes and further suggest that these species might shutdown their energy-consuming ribosomal machinery while dormant as spores by silencing of the rRNA genes using both 5mC/5hmC methylation and facultative heterochromatin formation at these loci.</description><identifier>ISSN: 1471-2164</identifier><identifier>EISSN: 1471-2164</identifier><identifier>DOI: 10.1186/s12864-023-09331-3</identifier><identifier>PMID: 37142951</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Chromosomes ; Computational biology ; Control ; Cores ; DNA methylation ; Encephalitozoon ; Encephalitozoon - genetics ; Epigenesis, Genetic ; Epigenetic inheritance ; Epigenetics ; Eukaryotes ; Gene loci ; Genes ; Genetic research ; Genome, Fungal ; Genomes ; Genomics ; Health aspects ; Heterochromatin ; Heterochromatin - genetics ; Humans ; Identification and classification ; Intracellular ; Maintenance ; Measurement ; Methods ; Methylation ; Microsporidia ; Nucleotides ; Pathogens ; Protein structure ; Protein structure prediction ; Proteins ; Ribosomal RNA ; RNA polymerase ; rRNA ; Spores ; Telomerase ; Telomere - genetics ; Telomeres ; Yeast</subject><ispartof>BMC genomics, 2023-05, Vol.24 (1), p.237-19, Article 237</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c598t-b7714ba5bb4f6f46194ecb97b21f4cf911783d5de98abe04c76b0e69347bdd4c3</citedby><cites>FETCH-LOGICAL-c598t-b7714ba5bb4f6f46194ecb97b21f4cf911783d5de98abe04c76b0e69347bdd4c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158259/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2815558876?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37142951$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mascarenhas Dos Santos, Anne Caroline</creatorcontrib><creatorcontrib>Julian, Alexander Thomas</creatorcontrib><creatorcontrib>Liang, Pingdong</creatorcontrib><creatorcontrib>Juárez, Oscar</creatorcontrib><creatorcontrib>Pombert, Jean-François</creatorcontrib><title>Telomere-to-Telomere genome assemblies of human-infecting Encephalitozoon species</title><title>BMC genomics</title><addtitle>BMC Genomics</addtitle><description>Microsporidia are diverse spore forming, fungal-related obligate intracellular pathogens infecting a wide range of hosts. This diversity is reflected at the genome level with sizes varying by an order of magnitude, ranging from less than 3 Mb in Encephalitozoon species (the smallest known in eukaryotes) to more than 50 Mb in Edhazardia spp. As a paradigm of genome reduction in eukaryotes, the small Encephalitozoon genomes have attracted much attention with investigations revealing gene dense, repeat- and intron-poor genomes characterized by a thorough pruning of molecular functions no longer relevant to their obligate intracellular lifestyle. However, because no Encephalitozoon genome has been sequenced from telomere-to-telomere and since no methylation data is available for these species, our understanding of their overall genetic and epigenetic architectures is incomplete.
In this study, we sequenced the complete genomes from telomere-to-telomere of three human-infecting Encephalitozoon spp. -E. intestinalis ATCC 50506, E. hellem ATCC 50604 and E. cuniculi ATCC 50602- using short and long read platforms and leveraged the data generated as part of the sequencing process to investigate the presence of epigenetic markers in these genomes. We also used a mixture of sequence- and structure-based computational approaches, including protein structure prediction, to help identify which Encephalitozoon proteins are involved in telomere maintenance, epigenetic regulation, and heterochromatin formation.
The Encephalitozoon chromosomes were found capped by TTAGG 5-mer telomeric repeats followed by telomere associated repeat elements (TAREs) flanking hypermethylated ribosomal RNA (rRNA) gene loci featuring 5-methylcytosines (5mC) and 5-hemimethylcytosines (5hmC), themselves followed by lesser methylated subtelomeres and hypomethylated chromosome cores. Strong nucleotide biases were identified between the telomeres/subtelomeres and chromosome cores with significant changes in GC/AT, GT/AC and GA/CT contents. The presence of several genes coding for proteins essential to telomere maintenance, epigenetic regulation, and heterochromatin formation was further confirmed in the Encephalitozoon genomes.
Altogether, our results strongly support the subtelomeres as sites of heterochromatin formation in Encephalitozoon genomes and further suggest that these species might shutdown their energy-consuming ribosomal machinery while dormant as spores by silencing of the rRNA genes using both 5mC/5hmC methylation and facultative heterochromatin formation at these loci.</description><subject>Analysis</subject><subject>Chromosomes</subject><subject>Computational biology</subject><subject>Control</subject><subject>Cores</subject><subject>DNA methylation</subject><subject>Encephalitozoon</subject><subject>Encephalitozoon - genetics</subject><subject>Epigenesis, Genetic</subject><subject>Epigenetic inheritance</subject><subject>Epigenetics</subject><subject>Eukaryotes</subject><subject>Gene loci</subject><subject>Genes</subject><subject>Genetic research</subject><subject>Genome, Fungal</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>Heterochromatin</subject><subject>Heterochromatin - genetics</subject><subject>Humans</subject><subject>Identification and classification</subject><subject>Intracellular</subject><subject>Maintenance</subject><subject>Measurement</subject><subject>Methods</subject><subject>Methylation</subject><subject>Microsporidia</subject><subject>Nucleotides</subject><subject>Pathogens</subject><subject>Protein structure</subject><subject>Protein structure prediction</subject><subject>Proteins</subject><subject>Ribosomal RNA</subject><subject>RNA polymerase</subject><subject>rRNA</subject><subject>Spores</subject><subject>Telomerase</subject><subject>Telomere - genetics</subject><subject>Telomeres</subject><subject>Yeast</subject><issn>1471-2164</issn><issn>1471-2164</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQhiMEomXhD3BAkbjAIcWfiX1CVdXCSpUQUM6W7YyzXiX2EicV8Ovr7balQcgHj8bPvB6_nqJ4jdEJxqL-kDARNasQoRWSlOKKPimOMWtwRXDNnj6Kj4oXKW0Rwo0g_HlxRBvMiOT4uPh6BX0cYIRqitV9XHYQclDqlGAwvYdURldu5kGHygcHdvKhK8-Dhd1G936Kf2IMZdqBzejL4pnTfYJXd_uq-HFxfnX2ubr88ml9dnpZWS7FVJkm92A0N4a52rEaSwbWyMYQ7Jh1EudeactbkEIbQMw2tUFQS8oa07bM0lWxPui2UW_VbvSDHn-rqL26TcSxU3qcvO1BcSINF4wi0RJGhdENosgSrk3rDG9d1vp40NrNZoDWQphG3S9ElyfBb1QXrxVGmGdLZVZ4d6cwxp8zpEkNPlnoex0gzkkRgZHEdZ0_a1W8_QfdxnkM2as9xTkXoqn_Up3OL8iux3yx3Yuq04YJzDhFe-rkP1ReLQzexgDO5_yi4P2iIDMT_Jo6Paek1t-_LVlyYO0YUxrBPRiCkdpPoDpMoMqPUrcTqGguevPYyoeS-5GjNyoA1TA</recordid><startdate>20230504</startdate><enddate>20230504</enddate><creator>Mascarenhas Dos Santos, Anne Caroline</creator><creator>Julian, Alexander Thomas</creator><creator>Liang, Pingdong</creator><creator>Juárez, Oscar</creator><creator>Pombert, Jean-François</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230504</creationdate><title>Telomere-to-Telomere genome assemblies of human-infecting Encephalitozoon species</title><author>Mascarenhas Dos Santos, Anne Caroline ; Julian, Alexander Thomas ; Liang, Pingdong ; Juárez, Oscar ; Pombert, Jean-François</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c598t-b7714ba5bb4f6f46194ecb97b21f4cf911783d5de98abe04c76b0e69347bdd4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Analysis</topic><topic>Chromosomes</topic><topic>Computational biology</topic><topic>Control</topic><topic>Cores</topic><topic>DNA methylation</topic><topic>Encephalitozoon</topic><topic>Encephalitozoon - genetics</topic><topic>Epigenesis, Genetic</topic><topic>Epigenetic inheritance</topic><topic>Epigenetics</topic><topic>Eukaryotes</topic><topic>Gene loci</topic><topic>Genes</topic><topic>Genetic research</topic><topic>Genome, Fungal</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Health aspects</topic><topic>Heterochromatin</topic><topic>Heterochromatin - genetics</topic><topic>Humans</topic><topic>Identification and classification</topic><topic>Intracellular</topic><topic>Maintenance</topic><topic>Measurement</topic><topic>Methods</topic><topic>Methylation</topic><topic>Microsporidia</topic><topic>Nucleotides</topic><topic>Pathogens</topic><topic>Protein structure</topic><topic>Protein structure prediction</topic><topic>Proteins</topic><topic>Ribosomal RNA</topic><topic>RNA polymerase</topic><topic>rRNA</topic><topic>Spores</topic><topic>Telomerase</topic><topic>Telomere - genetics</topic><topic>Telomeres</topic><topic>Yeast</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mascarenhas Dos Santos, Anne Caroline</creatorcontrib><creatorcontrib>Julian, Alexander Thomas</creatorcontrib><creatorcontrib>Liang, Pingdong</creatorcontrib><creatorcontrib>Juárez, Oscar</creatorcontrib><creatorcontrib>Pombert, Jean-François</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>BMC genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mascarenhas Dos Santos, Anne Caroline</au><au>Julian, Alexander Thomas</au><au>Liang, Pingdong</au><au>Juárez, Oscar</au><au>Pombert, Jean-François</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Telomere-to-Telomere genome assemblies of human-infecting Encephalitozoon species</atitle><jtitle>BMC genomics</jtitle><addtitle>BMC Genomics</addtitle><date>2023-05-04</date><risdate>2023</risdate><volume>24</volume><issue>1</issue><spage>237</spage><epage>19</epage><pages>237-19</pages><artnum>237</artnum><issn>1471-2164</issn><eissn>1471-2164</eissn><abstract>Microsporidia are diverse spore forming, fungal-related obligate intracellular pathogens infecting a wide range of hosts. This diversity is reflected at the genome level with sizes varying by an order of magnitude, ranging from less than 3 Mb in Encephalitozoon species (the smallest known in eukaryotes) to more than 50 Mb in Edhazardia spp. As a paradigm of genome reduction in eukaryotes, the small Encephalitozoon genomes have attracted much attention with investigations revealing gene dense, repeat- and intron-poor genomes characterized by a thorough pruning of molecular functions no longer relevant to their obligate intracellular lifestyle. However, because no Encephalitozoon genome has been sequenced from telomere-to-telomere and since no methylation data is available for these species, our understanding of their overall genetic and epigenetic architectures is incomplete.
In this study, we sequenced the complete genomes from telomere-to-telomere of three human-infecting Encephalitozoon spp. -E. intestinalis ATCC 50506, E. hellem ATCC 50604 and E. cuniculi ATCC 50602- using short and long read platforms and leveraged the data generated as part of the sequencing process to investigate the presence of epigenetic markers in these genomes. We also used a mixture of sequence- and structure-based computational approaches, including protein structure prediction, to help identify which Encephalitozoon proteins are involved in telomere maintenance, epigenetic regulation, and heterochromatin formation.
The Encephalitozoon chromosomes were found capped by TTAGG 5-mer telomeric repeats followed by telomere associated repeat elements (TAREs) flanking hypermethylated ribosomal RNA (rRNA) gene loci featuring 5-methylcytosines (5mC) and 5-hemimethylcytosines (5hmC), themselves followed by lesser methylated subtelomeres and hypomethylated chromosome cores. Strong nucleotide biases were identified between the telomeres/subtelomeres and chromosome cores with significant changes in GC/AT, GT/AC and GA/CT contents. The presence of several genes coding for proteins essential to telomere maintenance, epigenetic regulation, and heterochromatin formation was further confirmed in the Encephalitozoon genomes.
Altogether, our results strongly support the subtelomeres as sites of heterochromatin formation in Encephalitozoon genomes and further suggest that these species might shutdown their energy-consuming ribosomal machinery while dormant as spores by silencing of the rRNA genes using both 5mC/5hmC methylation and facultative heterochromatin formation at these loci.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37142951</pmid><doi>10.1186/s12864-023-09331-3</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Chromosomes Computational biology Control Cores DNA methylation Encephalitozoon Encephalitozoon - genetics Epigenesis, Genetic Epigenetic inheritance Epigenetics Eukaryotes Gene loci Genes Genetic research Genome, Fungal Genomes Genomics Health aspects Heterochromatin Heterochromatin - genetics Humans Identification and classification Intracellular Maintenance Measurement Methods Methylation Microsporidia Nucleotides Pathogens Protein structure Protein structure prediction Proteins Ribosomal RNA RNA polymerase rRNA Spores Telomerase Telomere - genetics Telomeres Yeast |
title | Telomere-to-Telomere genome assemblies of human-infecting Encephalitozoon species |
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