Mechanical stress affects dynamics and rheology of the human genome
Material properties of the genome are critical for proper cellular function - they directly affect timescales and length scales of DNA transactions such as transcription, replication and DNA repair, which in turn impact all cellular processes via the central dogma of molecular biology. Hence, elucid...
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description | Material properties of the genome are critical for proper cellular function - they directly affect timescales and length scales of DNA transactions such as transcription, replication and DNA repair, which in turn impact all cellular processes
via
the central dogma of molecular biology. Hence, elucidating the genome's rheology
in vivo
may help reveal physical principles underlying the genome's organization and function. Here, we present a novel noninvasive approach to study the genome's rheology and its response to mechanical stress in form of nuclear injection in live human cells. Specifically, we use Displacement Correlation Spectroscopy to map nucleus-wide genomic motions pre/post injection, during which we deposit rheological probes inside the cell nucleus. While the genomic motions inform on the bulk rheology of the genome pre/post injection, the probe's motion informs on the local rheology of its surroundings. Our results reveal that mechanical stress of injection leads to local as well as nucleus-wide changes in the genome's compaction, dynamics and rheology. We find that the genome pre-injection exhibits subdiffusive motions, which are coherent over several micrometers. In contrast, genomic motions post-injection become faster and uncorrelated, moreover, the genome becomes less compact and more viscous across the entire nucleus. In addition, we use the injected particles as rheological probes and find the genome to condense locally around them, mounting a local elastic response. Taken together, our results show that mechanical stress alters both dynamics and material properties of the genome. These changes are consistent with those observed upon DNA damage, suggesting that the genome experiences similar effects during the injection process.
Using a novel noninvasive approach, we measure dynamics and rheology of the genome in live human cells before and after applying mechanical stress. We find that mechanical stress alters both dynamics and material properties of the genome. |
doi_str_mv | 10.1039/d1sm00983d |
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via
the central dogma of molecular biology. Hence, elucidating the genome's rheology
in vivo
may help reveal physical principles underlying the genome's organization and function. Here, we present a novel noninvasive approach to study the genome's rheology and its response to mechanical stress in form of nuclear injection in live human cells. Specifically, we use Displacement Correlation Spectroscopy to map nucleus-wide genomic motions pre/post injection, during which we deposit rheological probes inside the cell nucleus. While the genomic motions inform on the bulk rheology of the genome pre/post injection, the probe's motion informs on the local rheology of its surroundings. Our results reveal that mechanical stress of injection leads to local as well as nucleus-wide changes in the genome's compaction, dynamics and rheology. We find that the genome pre-injection exhibits subdiffusive motions, which are coherent over several micrometers. In contrast, genomic motions post-injection become faster and uncorrelated, moreover, the genome becomes less compact and more viscous across the entire nucleus. In addition, we use the injected particles as rheological probes and find the genome to condense locally around them, mounting a local elastic response. Taken together, our results show that mechanical stress alters both dynamics and material properties of the genome. These changes are consistent with those observed upon DNA damage, suggesting that the genome experiences similar effects during the injection process.
Using a novel noninvasive approach, we measure dynamics and rheology of the genome in live human cells before and after applying mechanical stress. We find that mechanical stress alters both dynamics and material properties of the genome.</description><identifier>ISSN: 1744-683X</identifier><identifier>EISSN: 1744-6848</identifier><identifier>DOI: 10.1039/d1sm00983d</identifier><identifier>PMID: 34874386</identifier><language>eng</language><publisher>CAMBRIDGE: Royal Soc Chemistry</publisher><subject>Cell Nucleus ; Chemistry ; Chemistry, Physical ; Deoxyribonucleic acid ; DNA ; DNA - genetics ; DNA biosynthesis ; DNA damage ; DNA probes ; DNA repair ; Genome, Human ; Genomes ; Genomics ; Humans ; Injection ; Material properties ; Materials Science ; Materials Science, Multidisciplinary ; Micrometers ; Molecular biology ; Nuclei (cytology) ; Physical Sciences ; Physics ; Physics, Multidisciplinary ; Polymer Science ; Probes ; Rheological properties ; Rheology ; Science & Technology ; Spectroscopy ; Stress ; Stress, Mechanical ; Technology ; Transcription</subject><ispartof>Soft matter, 2021-12, Vol.18 (1), p.17-116</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>7</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000727608800001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c337t-f5c8c025c0feeb18552787c2adfddc2a981e5af9951750d49ab550a2563600b03</citedby><cites>FETCH-LOGICAL-c337t-f5c8c025c0feeb18552787c2adfddc2a981e5af9951750d49ab550a2563600b03</cites><orcidid>0000-0002-4619-4424 ; 0000-0002-5958-7200</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930,39263</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34874386$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Caragine, Christina M</creatorcontrib><creatorcontrib>Kanellakopoulos, Nikitas</creatorcontrib><creatorcontrib>Zidovska, Alexandra</creatorcontrib><title>Mechanical stress affects dynamics and rheology of the human genome</title><title>Soft matter</title><addtitle>SOFT MATTER</addtitle><addtitle>Soft Matter</addtitle><description>Material properties of the genome are critical for proper cellular function - they directly affect timescales and length scales of DNA transactions such as transcription, replication and DNA repair, which in turn impact all cellular processes
via
the central dogma of molecular biology. Hence, elucidating the genome's rheology
in vivo
may help reveal physical principles underlying the genome's organization and function. Here, we present a novel noninvasive approach to study the genome's rheology and its response to mechanical stress in form of nuclear injection in live human cells. Specifically, we use Displacement Correlation Spectroscopy to map nucleus-wide genomic motions pre/post injection, during which we deposit rheological probes inside the cell nucleus. While the genomic motions inform on the bulk rheology of the genome pre/post injection, the probe's motion informs on the local rheology of its surroundings. Our results reveal that mechanical stress of injection leads to local as well as nucleus-wide changes in the genome's compaction, dynamics and rheology. We find that the genome pre-injection exhibits subdiffusive motions, which are coherent over several micrometers. In contrast, genomic motions post-injection become faster and uncorrelated, moreover, the genome becomes less compact and more viscous across the entire nucleus. In addition, we use the injected particles as rheological probes and find the genome to condense locally around them, mounting a local elastic response. Taken together, our results show that mechanical stress alters both dynamics and material properties of the genome. These changes are consistent with those observed upon DNA damage, suggesting that the genome experiences similar effects during the injection process.
Using a novel noninvasive approach, we measure dynamics and rheology of the genome in live human cells before and after applying mechanical stress. We find that mechanical stress alters both dynamics and material properties of the genome.</description><subject>Cell Nucleus</subject><subject>Chemistry</subject><subject>Chemistry, Physical</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA - genetics</subject><subject>DNA biosynthesis</subject><subject>DNA damage</subject><subject>DNA probes</subject><subject>DNA repair</subject><subject>Genome, Human</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Humans</subject><subject>Injection</subject><subject>Material properties</subject><subject>Materials Science</subject><subject>Materials Science, Multidisciplinary</subject><subject>Micrometers</subject><subject>Molecular biology</subject><subject>Nuclei (cytology)</subject><subject>Physical Sciences</subject><subject>Physics</subject><subject>Physics, Multidisciplinary</subject><subject>Polymer Science</subject><subject>Probes</subject><subject>Rheological properties</subject><subject>Rheology</subject><subject>Science & Technology</subject><subject>Spectroscopy</subject><subject>Stress</subject><subject>Stress, Mechanical</subject><subject>Technology</subject><subject>Transcription</subject><issn>1744-683X</issn><issn>1744-6848</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><sourceid>EIF</sourceid><recordid>eNqN0kFLHDEUB_BQKu7WeundMtBLUVZfJpNJ5ihjrYLioRW8DZnkxZ1lJlmTGcp--8aubsGTp_cIv_8jPB4hXyicUmDVmaFxAKgkMx_InIqiWJSykB93PXuYkU8xrgCYLGi5T2askKJgspyT-hb1UrlOqz6LY8AYM2Ut6jFmZuPU0On04EwWluh7_7jJvM3GJWbLaVAue0TnB_xM9qzqIx6-1ANyf_njd321uLn7eV2f3yw0Y2JcWK6lhpxrsIgtlZznQgqdK2ONSaWSFLmyVcWp4GCKSrWcg8p5yUqAFtgB-b6duw7-acI4NkMXNfa9cuin2OQlCC6BiSrRb2_oyk_Bpd8lRXNGKxAsqeOt0sHHGNA269ANKmwaCs3zapsL-uv232ovEv76MnJqBzQ7-rrLBE624A-23kbdodO4YwAgclGClKkDmrR8v667UY2dd7Wf3JiiR9toiHqX-H8E7C8fGp0n</recordid><startdate>20211222</startdate><enddate>20211222</enddate><creator>Caragine, Christina M</creator><creator>Kanellakopoulos, Nikitas</creator><creator>Zidovska, Alexandra</creator><general>Royal Soc Chemistry</general><general>Royal Society of Chemistry</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4619-4424</orcidid><orcidid>https://orcid.org/0000-0002-5958-7200</orcidid></search><sort><creationdate>20211222</creationdate><title>Mechanical stress affects dynamics and rheology of the human genome</title><author>Caragine, Christina M ; Kanellakopoulos, Nikitas ; Zidovska, Alexandra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-f5c8c025c0feeb18552787c2adfddc2a981e5af9951750d49ab550a2563600b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Cell Nucleus</topic><topic>Chemistry</topic><topic>Chemistry, Physical</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA - genetics</topic><topic>DNA biosynthesis</topic><topic>DNA damage</topic><topic>DNA probes</topic><topic>DNA repair</topic><topic>Genome, Human</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Humans</topic><topic>Injection</topic><topic>Material properties</topic><topic>Materials Science</topic><topic>Materials Science, Multidisciplinary</topic><topic>Micrometers</topic><topic>Molecular biology</topic><topic>Nuclei (cytology)</topic><topic>Physical Sciences</topic><topic>Physics</topic><topic>Physics, Multidisciplinary</topic><topic>Polymer Science</topic><topic>Probes</topic><topic>Rheological properties</topic><topic>Rheology</topic><topic>Science & Technology</topic><topic>Spectroscopy</topic><topic>Stress</topic><topic>Stress, Mechanical</topic><topic>Technology</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Caragine, Christina M</creatorcontrib><creatorcontrib>Kanellakopoulos, Nikitas</creatorcontrib><creatorcontrib>Zidovska, Alexandra</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Soft matter</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Caragine, Christina M</au><au>Kanellakopoulos, Nikitas</au><au>Zidovska, Alexandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanical stress affects dynamics and rheology of the human genome</atitle><jtitle>Soft matter</jtitle><stitle>SOFT MATTER</stitle><addtitle>Soft Matter</addtitle><date>2021-12-22</date><risdate>2021</risdate><volume>18</volume><issue>1</issue><spage>17</spage><epage>116</epage><pages>17-116</pages><issn>1744-683X</issn><eissn>1744-6848</eissn><abstract>Material properties of the genome are critical for proper cellular function - they directly affect timescales and length scales of DNA transactions such as transcription, replication and DNA repair, which in turn impact all cellular processes
via
the central dogma of molecular biology. Hence, elucidating the genome's rheology
in vivo
may help reveal physical principles underlying the genome's organization and function. Here, we present a novel noninvasive approach to study the genome's rheology and its response to mechanical stress in form of nuclear injection in live human cells. Specifically, we use Displacement Correlation Spectroscopy to map nucleus-wide genomic motions pre/post injection, during which we deposit rheological probes inside the cell nucleus. While the genomic motions inform on the bulk rheology of the genome pre/post injection, the probe's motion informs on the local rheology of its surroundings. Our results reveal that mechanical stress of injection leads to local as well as nucleus-wide changes in the genome's compaction, dynamics and rheology. We find that the genome pre-injection exhibits subdiffusive motions, which are coherent over several micrometers. In contrast, genomic motions post-injection become faster and uncorrelated, moreover, the genome becomes less compact and more viscous across the entire nucleus. In addition, we use the injected particles as rheological probes and find the genome to condense locally around them, mounting a local elastic response. Taken together, our results show that mechanical stress alters both dynamics and material properties of the genome. These changes are consistent with those observed upon DNA damage, suggesting that the genome experiences similar effects during the injection process.
Using a novel noninvasive approach, we measure dynamics and rheology of the genome in live human cells before and after applying mechanical stress. We find that mechanical stress alters both dynamics and material properties of the genome.</abstract><cop>CAMBRIDGE</cop><pub>Royal Soc Chemistry</pub><pmid>34874386</pmid><doi>10.1039/d1sm00983d</doi><orcidid>https://orcid.org/0000-0002-4619-4424</orcidid><orcidid>https://orcid.org/0000-0002-5958-7200</orcidid></addata></record> |
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subjects | Cell Nucleus Chemistry Chemistry, Physical Deoxyribonucleic acid DNA DNA - genetics DNA biosynthesis DNA damage DNA probes DNA repair Genome, Human Genomes Genomics Humans Injection Material properties Materials Science Materials Science, Multidisciplinary Micrometers Molecular biology Nuclei (cytology) Physical Sciences Physics Physics, Multidisciplinary Polymer Science Probes Rheological properties Rheology Science & Technology Spectroscopy Stress Stress, Mechanical Technology Transcription |
title | Mechanical stress affects dynamics and rheology of the human genome |
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