Genome-wide transcription and the implications for genomic organization
Key Points In-depth analyses of the transcriptional outputs of eukaryotic genomes suggest that the information content of a genome is complex, and that this complexity manifests itself at two levels: the fraction of the genome that is devoted to encoding functional elements is higher than expected,...
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description | Key Points
In-depth analyses of the transcriptional outputs of eukaryotic genomes suggest that the information content of a genome is complex, and that this complexity manifests itself at two levels: the fraction of the genome that is devoted to encoding functional elements is higher than expected, and multiple functional elements can exist in a single region.
The architecture of the eukaryotic transcriptome is clearly much more complex than could have been anticipated in terms of the number of nucleotides that are transcribed and the final arrangements of nucleotides that are present in mature processed RNA molecules.
The complexity of genomic organization suggests that the currently accepted model, by which each region of DNA carries a single discrete function, must be re-evaluated, and an interleaved model for the arrangement of functional elements is more likely to represent the informational content of eukaryotic genomes.
Despite the potential problems that are presented by use of the same genomic space for multiple purposes, the following advantages are brought by this complex genomic organization: an increase in protein-coding transcript diversity; a widespread adoption of RNA transcripts as regulatory agents; and a reliance on transcription as a regulatory process.
On a global level, an interleaved genomic organization of functional elements seems to be preserved in different kingdoms, and the arrangement of specific overlapping functional elements is preserved among different species. This suggests that such a model does indeed provide advantages throughout evolution.
Mutations at non-canonical sites, such as intronic regions that lie distal from splice sites, can affect fitness if they involve internal promoter regions, an exon of an overlapping transcript or a short RNA.
Genome-wide analyses of transcriptional output in eukaryotes have revealed an unanticipated transcriptome complexity. These findings imply a complex, interleaved genomic organization, in which individual sequences carry multiple and overlapping informational content. The authors discuss the evidence for, and functional and evolutionary consequences of, this organization.
Recent evidence of genome-wide transcription in several species indicates that the amount of transcription that occurs cannot be entirely accounted for by current sets of genome-wide annotations. Evidence indicates that most of both strands of the human genome might be transcribed, implying extensive overlap of |
doi_str_mv | 10.1038/nrg2083 |
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In-depth analyses of the transcriptional outputs of eukaryotic genomes suggest that the information content of a genome is complex, and that this complexity manifests itself at two levels: the fraction of the genome that is devoted to encoding functional elements is higher than expected, and multiple functional elements can exist in a single region.
The architecture of the eukaryotic transcriptome is clearly much more complex than could have been anticipated in terms of the number of nucleotides that are transcribed and the final arrangements of nucleotides that are present in mature processed RNA molecules.
The complexity of genomic organization suggests that the currently accepted model, by which each region of DNA carries a single discrete function, must be re-evaluated, and an interleaved model for the arrangement of functional elements is more likely to represent the informational content of eukaryotic genomes.
Despite the potential problems that are presented by use of the same genomic space for multiple purposes, the following advantages are brought by this complex genomic organization: an increase in protein-coding transcript diversity; a widespread adoption of RNA transcripts as regulatory agents; and a reliance on transcription as a regulatory process.
On a global level, an interleaved genomic organization of functional elements seems to be preserved in different kingdoms, and the arrangement of specific overlapping functional elements is preserved among different species. This suggests that such a model does indeed provide advantages throughout evolution.
Mutations at non-canonical sites, such as intronic regions that lie distal from splice sites, can affect fitness if they involve internal promoter regions, an exon of an overlapping transcript or a short RNA.
Genome-wide analyses of transcriptional output in eukaryotes have revealed an unanticipated transcriptome complexity. These findings imply a complex, interleaved genomic organization, in which individual sequences carry multiple and overlapping informational content. The authors discuss the evidence for, and functional and evolutionary consequences of, this organization.
Recent evidence of genome-wide transcription in several species indicates that the amount of transcription that occurs cannot be entirely accounted for by current sets of genome-wide annotations. Evidence indicates that most of both strands of the human genome might be transcribed, implying extensive overlap of transcriptional units and regulatory elements. These observations suggest that genomic architecture is not colinear, but is instead interleaved and modular, and that the same genomic sequences are multifunctional: that is, used for multiple independently regulated transcripts and as regulatory regions. What are the implications and consequences of such an interleaved genomic architecture in terms of increased information content, transcriptional complexity, evolution and disease states?</description><identifier>ISSN: 1471-0056</identifier><identifier>EISSN: 1471-0064</identifier><identifier>DOI: 10.1038/nrg2083</identifier><identifier>PMID: 17486121</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Agriculture ; Animal Genetics and Genomics ; Animals ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Evolution, Molecular ; Fundamental and applied biological sciences. Psychology ; Gene Expression ; Gene Function ; Genes ; Genes, Regulator ; Genetic regulation ; Genetic Techniques ; Genetic transcription ; Genetics of eukaryotes. Biological and molecular evolution ; Genome ; Genome, Human ; Genomes ; Human Genetics ; Humans ; Models, Genetic ; Molecular and cellular biology ; Molecular evolution ; Molecular genetics ; Physiological aspects ; Promoter Regions, Genetic ; Proteins ; review-article ; RNA - genetics ; RNA polymerase ; RNA, Antisense - genetics ; Signal Transduction - genetics ; Transcription, Genetic ; Transcription. Transcription factor. Splicing. Rna processing</subject><ispartof>Nature reviews. Genetics, 2007-06, Vol.8 (6), p.413-423</ispartof><rights>Springer Nature Limited 2007</rights><rights>2007 INIST-CNRS</rights><rights>COPYRIGHT 2007 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Jun 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c598t-3665c2ead3631f9deed4097661ea2255c720111045c9576ff387b0221137b873</citedby><cites>FETCH-LOGICAL-c598t-3665c2ead3631f9deed4097661ea2255c720111045c9576ff387b0221137b873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nrg2083$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nrg2083$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18756330$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17486121$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kapranov, Philipp</creatorcontrib><creatorcontrib>Willingham, Aarron T.</creatorcontrib><creatorcontrib>Gingeras, Thomas R.</creatorcontrib><title>Genome-wide transcription and the implications for genomic organization</title><title>Nature reviews. Genetics</title><addtitle>Nat Rev Genet</addtitle><addtitle>Nat Rev Genet</addtitle><description>Key Points
In-depth analyses of the transcriptional outputs of eukaryotic genomes suggest that the information content of a genome is complex, and that this complexity manifests itself at two levels: the fraction of the genome that is devoted to encoding functional elements is higher than expected, and multiple functional elements can exist in a single region.
The architecture of the eukaryotic transcriptome is clearly much more complex than could have been anticipated in terms of the number of nucleotides that are transcribed and the final arrangements of nucleotides that are present in mature processed RNA molecules.
The complexity of genomic organization suggests that the currently accepted model, by which each region of DNA carries a single discrete function, must be re-evaluated, and an interleaved model for the arrangement of functional elements is more likely to represent the informational content of eukaryotic genomes.
Despite the potential problems that are presented by use of the same genomic space for multiple purposes, the following advantages are brought by this complex genomic organization: an increase in protein-coding transcript diversity; a widespread adoption of RNA transcripts as regulatory agents; and a reliance on transcription as a regulatory process.
On a global level, an interleaved genomic organization of functional elements seems to be preserved in different kingdoms, and the arrangement of specific overlapping functional elements is preserved among different species. This suggests that such a model does indeed provide advantages throughout evolution.
Mutations at non-canonical sites, such as intronic regions that lie distal from splice sites, can affect fitness if they involve internal promoter regions, an exon of an overlapping transcript or a short RNA.
Genome-wide analyses of transcriptional output in eukaryotes have revealed an unanticipated transcriptome complexity. These findings imply a complex, interleaved genomic organization, in which individual sequences carry multiple and overlapping informational content. The authors discuss the evidence for, and functional and evolutionary consequences of, this organization.
Recent evidence of genome-wide transcription in several species indicates that the amount of transcription that occurs cannot be entirely accounted for by current sets of genome-wide annotations. Evidence indicates that most of both strands of the human genome might be transcribed, implying extensive overlap of transcriptional units and regulatory elements. These observations suggest that genomic architecture is not colinear, but is instead interleaved and modular, and that the same genomic sequences are multifunctional: that is, used for multiple independently regulated transcripts and as regulatory regions. What are the implications and consequences of such an interleaved genomic architecture in terms of increased information content, transcriptional complexity, evolution and disease states?</description><subject>Agriculture</subject><subject>Animal Genetics and Genomics</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Evolution, Molecular</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression</subject><subject>Gene Function</subject><subject>Genes</subject><subject>Genes, Regulator</subject><subject>Genetic regulation</subject><subject>Genetic Techniques</subject><subject>Genetic transcription</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Genome</subject><subject>Genome, Human</subject><subject>Genomes</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Models, Genetic</subject><subject>Molecular and cellular biology</subject><subject>Molecular evolution</subject><subject>Molecular genetics</subject><subject>Physiological aspects</subject><subject>Promoter Regions, Genetic</subject><subject>Proteins</subject><subject>review-article</subject><subject>RNA - genetics</subject><subject>RNA polymerase</subject><subject>RNA, Antisense - genetics</subject><subject>Signal Transduction - genetics</subject><subject>Transcription, Genetic</subject><subject>Transcription. Transcription factor. Splicing. Rna processing</subject><issn>1471-0056</issn><issn>1471-0064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqF0l9r1TAUAPAiiptT_AZSlE196MxJmj99HEOvg4Ggey-56WlvRptckxZ1n950t3i9Q5A8JCS_c0JOTpa9BHIOhKkPLnSUKPYoO4ZSQkGIKB__WXNxlD2L8ZYQECDZ0-wIZKkEUDjOVit0fsDih20wH4N20QS7Ha13uXZNPm4wt8O2t0bPezFvfci7OcSa3IdOO3t3f_I8e9LqPuKLZT7Jbj59vLn8XFx_WV1dXlwXhldqLJgQ3FDUDRMM2qpBbEpSSSEANaWcG0kJAJCSm4pL0bZMyTWhFIDJtZLsJDvbpd0G_33CONaDjQb7Xjv0U6wl4SA4Ef-FlMiqVHLO-PoBvPVTcOkNNaVMlhVQldCbHep0j7V1rU-lMnPG-gLUPHhVJnX-D5VGg6lc3mFr0_5BwPuDgGRG_Dl2eoqxvvr29dCe_WU3qPtxE30_3X_LIXy7gyb4GAO29TbYQYdfNZB6bpZ6aZYkXy1Pn9YDNnu3dEcCpwvQ0ei-Te1hbNw7JblgjCT3budiOnIdhn0NH975G_mMzt4</recordid><startdate>20070601</startdate><enddate>20070601</enddate><creator>Kapranov, Philipp</creator><creator>Willingham, Aarron T.</creator><creator>Gingeras, Thomas R.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</scope><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>7RV</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</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>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070601</creationdate><title>Genome-wide transcription and the implications for genomic organization</title><author>Kapranov, Philipp ; Willingham, Aarron T. ; Gingeras, Thomas R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c598t-3665c2ead3631f9deed4097661ea2255c720111045c9576ff387b0221137b873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Agriculture</topic><topic>Animal Genetics and Genomics</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Evolution, Molecular</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression</topic><topic>Gene Function</topic><topic>Genes</topic><topic>Genes, Regulator</topic><topic>Genetic regulation</topic><topic>Genetic Techniques</topic><topic>Genetic transcription</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Genome</topic><topic>Genome, Human</topic><topic>Genomes</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Models, Genetic</topic><topic>Molecular and cellular biology</topic><topic>Molecular evolution</topic><topic>Molecular genetics</topic><topic>Physiological aspects</topic><topic>Promoter Regions, Genetic</topic><topic>Proteins</topic><topic>review-article</topic><topic>RNA - genetics</topic><topic>RNA polymerase</topic><topic>RNA, Antisense - genetics</topic><topic>Signal Transduction - genetics</topic><topic>Transcription, Genetic</topic><topic>Transcription. Transcription factor. Splicing. Rna processing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kapranov, Philipp</creatorcontrib><creatorcontrib>Willingham, Aarron T.</creatorcontrib><creatorcontrib>Gingeras, Thomas R.</creatorcontrib><collection>Pascal-Francis</collection><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>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nature reviews. Genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kapranov, Philipp</au><au>Willingham, Aarron T.</au><au>Gingeras, Thomas R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome-wide transcription and the implications for genomic organization</atitle><jtitle>Nature reviews. Genetics</jtitle><stitle>Nat Rev Genet</stitle><addtitle>Nat Rev Genet</addtitle><date>2007-06-01</date><risdate>2007</risdate><volume>8</volume><issue>6</issue><spage>413</spage><epage>423</epage><pages>413-423</pages><issn>1471-0056</issn><eissn>1471-0064</eissn><abstract>Key Points
In-depth analyses of the transcriptional outputs of eukaryotic genomes suggest that the information content of a genome is complex, and that this complexity manifests itself at two levels: the fraction of the genome that is devoted to encoding functional elements is higher than expected, and multiple functional elements can exist in a single region.
The architecture of the eukaryotic transcriptome is clearly much more complex than could have been anticipated in terms of the number of nucleotides that are transcribed and the final arrangements of nucleotides that are present in mature processed RNA molecules.
The complexity of genomic organization suggests that the currently accepted model, by which each region of DNA carries a single discrete function, must be re-evaluated, and an interleaved model for the arrangement of functional elements is more likely to represent the informational content of eukaryotic genomes.
Despite the potential problems that are presented by use of the same genomic space for multiple purposes, the following advantages are brought by this complex genomic organization: an increase in protein-coding transcript diversity; a widespread adoption of RNA transcripts as regulatory agents; and a reliance on transcription as a regulatory process.
On a global level, an interleaved genomic organization of functional elements seems to be preserved in different kingdoms, and the arrangement of specific overlapping functional elements is preserved among different species. This suggests that such a model does indeed provide advantages throughout evolution.
Mutations at non-canonical sites, such as intronic regions that lie distal from splice sites, can affect fitness if they involve internal promoter regions, an exon of an overlapping transcript or a short RNA.
Genome-wide analyses of transcriptional output in eukaryotes have revealed an unanticipated transcriptome complexity. These findings imply a complex, interleaved genomic organization, in which individual sequences carry multiple and overlapping informational content. The authors discuss the evidence for, and functional and evolutionary consequences of, this organization.
Recent evidence of genome-wide transcription in several species indicates that the amount of transcription that occurs cannot be entirely accounted for by current sets of genome-wide annotations. Evidence indicates that most of both strands of the human genome might be transcribed, implying extensive overlap of transcriptional units and regulatory elements. These observations suggest that genomic architecture is not colinear, but is instead interleaved and modular, and that the same genomic sequences are multifunctional: that is, used for multiple independently regulated transcripts and as regulatory regions. What are the implications and consequences of such an interleaved genomic architecture in terms of increased information content, transcriptional complexity, evolution and disease states?</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>17486121</pmid><doi>10.1038/nrg2083</doi><tpages>11</tpages></addata></record> |
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subjects | Agriculture Animal Genetics and Genomics Animals Biological and medical sciences Biomedical and Life Sciences Biomedicine Cancer Research Evolution, Molecular Fundamental and applied biological sciences. Psychology Gene Expression Gene Function Genes Genes, Regulator Genetic regulation Genetic Techniques Genetic transcription Genetics of eukaryotes. Biological and molecular evolution Genome Genome, Human Genomes Human Genetics Humans Models, Genetic Molecular and cellular biology Molecular evolution Molecular genetics Physiological aspects Promoter Regions, Genetic Proteins review-article RNA - genetics RNA polymerase RNA, Antisense - genetics Signal Transduction - genetics Transcription, Genetic Transcription. Transcription factor. Splicing. Rna processing |
title | Genome-wide transcription and the implications for genomic organization |
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