Hit the brakes - a new perspective on the loop extrusion mechanism of cohesin and other SMC complexes
The three-dimensional structure of chromatin is determined by the action of protein complexes of the structural maintenance of chromosome (SMC) family. Eukaryotic cells contain three SMC complexes, cohesin, condensin, and a complex of Smc5 and Smc6. Initially, cohesin was linked to sister chromatid...
Gespeichert in:
Veröffentlicht in: | Journal of cell science 2021-01, Vol.134 (1) |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 1 |
container_start_page | |
container_title | Journal of cell science |
container_volume | 134 |
creator | Matityahu, Avi Onn, Itay |
description | The three-dimensional structure of chromatin is determined by the action of protein complexes of the structural maintenance of chromosome (SMC) family. Eukaryotic cells contain three SMC complexes, cohesin, condensin, and a complex of Smc5 and Smc6. Initially, cohesin was linked to sister chromatid cohesion, the process that ensures the fidelity of chromosome segregation in mitosis. In recent years, a second function in the organization of interphase chromatin into topologically associated domains has been determined, and loop extrusion has emerged as the leading mechanism of this process. Interestingly, fundamental mechanistic differences exist between mitotic tethering and loop extrusion. As distinct molecular switches that aim to suppress loop extrusion in different biological contexts have been identified, we hypothesize here that loop extrusion is the default biochemical activity of cohesin and that its suppression shifts cohesin into a tethering mode. With this model, we aim to provide an explanation for how loop extrusion and tethering can coexist in a single cohesin complex and also apply it to the other eukaryotic SMC complexes, describing both similarities and differences between them. Finally, we present model-derived molecular predictions that can be tested experimentally, thus offering a new perspective on the mechanisms by which SMC complexes shape the higher-order structure of chromatin. |
doi_str_mv | 10.1242/jcs.247577 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2476560992</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2476560992</sourcerecordid><originalsourceid>FETCH-LOGICAL-c323t-275e82a56de1cd86e0efff0f869f97a4582d162295721435e16e3c14a715ed373</originalsourceid><addsrcrecordid>eNo90E9LwzAYx_EgipvTiy9AchShM3-b5ihDnTDxoJ5Llj5hnW1Tk1bnu7fa6emBhw-_wxehc0rmlAl2vbVxzoSSSh2gKRVKJZpydYimhDCaaMn5BJ3EuCWEKKbVMZpwLqjWQk8RLMsOdxvA62DeIOIEG9zAJ24hxBZsV34A9s2vqLxvMey60MdyeNVgN6YpY429w9ZvIJYNNk2B_YADfn5cDN-6rWAH8RQdOVNFONvfGXq9u31ZLJPV0_3D4maVWM54lzAlIWNGpgVQW2QpEHDOEZel2mllhMxYQVPGtFSMCi6BpsAtFUZRCQVXfIYux902-PceYpfXZbRQVaYB38d8qJTKlGjNBno1Uht8jAFc3oayNuErpyT_yZoPWfMx64Av9rv9uobin_515N9ZfXJv</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2476560992</pqid></control><display><type>article</type><title>Hit the brakes - a new perspective on the loop extrusion mechanism of cohesin and other SMC complexes</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><source>Company of Biologists</source><creator>Matityahu, Avi ; Onn, Itay</creator><creatorcontrib>Matityahu, Avi ; Onn, Itay</creatorcontrib><description>The three-dimensional structure of chromatin is determined by the action of protein complexes of the structural maintenance of chromosome (SMC) family. Eukaryotic cells contain three SMC complexes, cohesin, condensin, and a complex of Smc5 and Smc6. Initially, cohesin was linked to sister chromatid cohesion, the process that ensures the fidelity of chromosome segregation in mitosis. In recent years, a second function in the organization of interphase chromatin into topologically associated domains has been determined, and loop extrusion has emerged as the leading mechanism of this process. Interestingly, fundamental mechanistic differences exist between mitotic tethering and loop extrusion. As distinct molecular switches that aim to suppress loop extrusion in different biological contexts have been identified, we hypothesize here that loop extrusion is the default biochemical activity of cohesin and that its suppression shifts cohesin into a tethering mode. With this model, we aim to provide an explanation for how loop extrusion and tethering can coexist in a single cohesin complex and also apply it to the other eukaryotic SMC complexes, describing both similarities and differences between them. Finally, we present model-derived molecular predictions that can be tested experimentally, thus offering a new perspective on the mechanisms by which SMC complexes shape the higher-order structure of chromatin.</description><identifier>ISSN: 0021-9533</identifier><identifier>EISSN: 1477-9137</identifier><identifier>DOI: 10.1242/jcs.247577</identifier><identifier>PMID: 33419949</identifier><language>eng</language><publisher>England</publisher><subject>Cell Cycle Proteins - genetics ; Chromosomal Proteins, Non-Histone - genetics ; Chromosomes ; Cohesins ; Mitosis</subject><ispartof>Journal of cell science, 2021-01, Vol.134 (1)</ispartof><rights>2021. Published by The Company of Biologists Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c323t-275e82a56de1cd86e0efff0f869f97a4582d162295721435e16e3c14a715ed373</citedby><cites>FETCH-LOGICAL-c323t-275e82a56de1cd86e0efff0f869f97a4582d162295721435e16e3c14a715ed373</cites><orcidid>0000-0002-7689-5520</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3676,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33419949$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matityahu, Avi</creatorcontrib><creatorcontrib>Onn, Itay</creatorcontrib><title>Hit the brakes - a new perspective on the loop extrusion mechanism of cohesin and other SMC complexes</title><title>Journal of cell science</title><addtitle>J Cell Sci</addtitle><description>The three-dimensional structure of chromatin is determined by the action of protein complexes of the structural maintenance of chromosome (SMC) family. Eukaryotic cells contain three SMC complexes, cohesin, condensin, and a complex of Smc5 and Smc6. Initially, cohesin was linked to sister chromatid cohesion, the process that ensures the fidelity of chromosome segregation in mitosis. In recent years, a second function in the organization of interphase chromatin into topologically associated domains has been determined, and loop extrusion has emerged as the leading mechanism of this process. Interestingly, fundamental mechanistic differences exist between mitotic tethering and loop extrusion. As distinct molecular switches that aim to suppress loop extrusion in different biological contexts have been identified, we hypothesize here that loop extrusion is the default biochemical activity of cohesin and that its suppression shifts cohesin into a tethering mode. With this model, we aim to provide an explanation for how loop extrusion and tethering can coexist in a single cohesin complex and also apply it to the other eukaryotic SMC complexes, describing both similarities and differences between them. Finally, we present model-derived molecular predictions that can be tested experimentally, thus offering a new perspective on the mechanisms by which SMC complexes shape the higher-order structure of chromatin.</description><subject>Cell Cycle Proteins - genetics</subject><subject>Chromosomal Proteins, Non-Histone - genetics</subject><subject>Chromosomes</subject><subject>Cohesins</subject><subject>Mitosis</subject><issn>0021-9533</issn><issn>1477-9137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo90E9LwzAYx_EgipvTiy9AchShM3-b5ihDnTDxoJ5Llj5hnW1Tk1bnu7fa6emBhw-_wxehc0rmlAl2vbVxzoSSSh2gKRVKJZpydYimhDCaaMn5BJ3EuCWEKKbVMZpwLqjWQk8RLMsOdxvA62DeIOIEG9zAJ24hxBZsV34A9s2vqLxvMey60MdyeNVgN6YpY429w9ZvIJYNNk2B_YADfn5cDN-6rWAH8RQdOVNFONvfGXq9u31ZLJPV0_3D4maVWM54lzAlIWNGpgVQW2QpEHDOEZel2mllhMxYQVPGtFSMCi6BpsAtFUZRCQVXfIYux902-PceYpfXZbRQVaYB38d8qJTKlGjNBno1Uht8jAFc3oayNuErpyT_yZoPWfMx64Av9rv9uobin_515N9ZfXJv</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Matityahu, Avi</creator><creator>Onn, Itay</creator><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>7X8</scope><orcidid>https://orcid.org/0000-0002-7689-5520</orcidid></search><sort><creationdate>20210101</creationdate><title>Hit the brakes - a new perspective on the loop extrusion mechanism of cohesin and other SMC complexes</title><author>Matityahu, Avi ; Onn, Itay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-275e82a56de1cd86e0efff0f869f97a4582d162295721435e16e3c14a715ed373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Cell Cycle Proteins - genetics</topic><topic>Chromosomal Proteins, Non-Histone - genetics</topic><topic>Chromosomes</topic><topic>Cohesins</topic><topic>Mitosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matityahu, Avi</creatorcontrib><creatorcontrib>Onn, Itay</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cell science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matityahu, Avi</au><au>Onn, Itay</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hit the brakes - a new perspective on the loop extrusion mechanism of cohesin and other SMC complexes</atitle><jtitle>Journal of cell science</jtitle><addtitle>J Cell Sci</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>134</volume><issue>1</issue><issn>0021-9533</issn><eissn>1477-9137</eissn><abstract>The three-dimensional structure of chromatin is determined by the action of protein complexes of the structural maintenance of chromosome (SMC) family. Eukaryotic cells contain three SMC complexes, cohesin, condensin, and a complex of Smc5 and Smc6. Initially, cohesin was linked to sister chromatid cohesion, the process that ensures the fidelity of chromosome segregation in mitosis. In recent years, a second function in the organization of interphase chromatin into topologically associated domains has been determined, and loop extrusion has emerged as the leading mechanism of this process. Interestingly, fundamental mechanistic differences exist between mitotic tethering and loop extrusion. As distinct molecular switches that aim to suppress loop extrusion in different biological contexts have been identified, we hypothesize here that loop extrusion is the default biochemical activity of cohesin and that its suppression shifts cohesin into a tethering mode. With this model, we aim to provide an explanation for how loop extrusion and tethering can coexist in a single cohesin complex and also apply it to the other eukaryotic SMC complexes, describing both similarities and differences between them. Finally, we present model-derived molecular predictions that can be tested experimentally, thus offering a new perspective on the mechanisms by which SMC complexes shape the higher-order structure of chromatin.</abstract><cop>England</cop><pmid>33419949</pmid><doi>10.1242/jcs.247577</doi><orcidid>https://orcid.org/0000-0002-7689-5520</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9533 |
ispartof | Journal of cell science, 2021-01, Vol.134 (1) |
issn | 0021-9533 1477-9137 |
language | eng |
recordid | cdi_proquest_miscellaneous_2476560992 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection; Company of Biologists |
subjects | Cell Cycle Proteins - genetics Chromosomal Proteins, Non-Histone - genetics Chromosomes Cohesins Mitosis |
title | Hit the brakes - a new perspective on the loop extrusion mechanism of cohesin and other SMC complexes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T11%3A29%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hit%20the%20brakes%20-%20a%20new%20perspective%20on%20the%20loop%20extrusion%20mechanism%20of%20cohesin%20and%20other%20SMC%20complexes&rft.jtitle=Journal%20of%20cell%20science&rft.au=Matityahu,%20Avi&rft.date=2021-01-01&rft.volume=134&rft.issue=1&rft.issn=0021-9533&rft.eissn=1477-9137&rft_id=info:doi/10.1242/jcs.247577&rft_dat=%3Cproquest_cross%3E2476560992%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2476560992&rft_id=info:pmid/33419949&rfr_iscdi=true |