Phenotypic screens identify SCAF1 as critical activator of RNAPII elongation and global transcription
Transcripts produced by RNA polymerase II (RNAPII) are fundamental for cellular responses to environmental changes. It is therefore no surprise that there exist multiple avenues for the regulation of this process. To explore the regulation mediated by RNAPII-interacting proteins, we used a small int...
Gespeichert in:
Veröffentlicht in: | Nucleic acids research 2024-12 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | Nucleic acids research |
container_volume | |
creator | Bhandare, Pranjali Narain, Ashwin Hofstetter, Julia Rummel, Teresa Wenzel, Julia Schülein-Völk, Christina Lamer, Stephanie Eilers, Ursula Schlosser, Andreas Eilers, Martin Erhard, Florian Wolf, Elmar |
description | Transcripts produced by RNA polymerase II (RNAPII) are fundamental for cellular responses to environmental changes. It is therefore no surprise that there exist multiple avenues for the regulation of this process. To explore the regulation mediated by RNAPII-interacting proteins, we used a small interfering RNA (siRNA)-based screen to systematically evaluate their influence on RNA synthesis. We identified several proteins that strongly affected RNAPII activity. We evaluated one of the top hits, SCAF1 (SR-related C-terminal domain-associated factor 1), using an auxin-inducible degradation system and sequencing approaches. In agreement with our screen results, acute depletion of SCAF1 decreased RNA synthesis, and showed an increase of Serine-2 phosphorylated-RNAPII (pS2-RNAPII). We found that the accumulation of pS2-RNAPII within the gene body occurred at GC-rich regions and was indicative of stalled RNAPII complexes. The accumulation of stalled RNAPII complexes was accompanied by reduced recruitment of initiating RNAPII, explaining the observed global decrease in transcriptional output. Furthermore, upon SCAF1 depletion, RNAPII complexes showed increased association with components of the proteasomal-degradation machinery. We concluded that in cells lacking SCAF1, RNAPII undergoes a rather interrupted passage, resulting in intervention by the proteasomal-degradation machinery to clear stalled RNAPII. While cells survive the compromised transcription caused by absence of SCAF1, further inhibition of proteasomal-degradation machinery is synthetically lethal. |
doi_str_mv | 10.1093/nar/gkae1219 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3147134422</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3147134422</sourcerecordid><originalsourceid>FETCH-LOGICAL-c216t-5478fcf12540ed48ac3b7ae476ea4fc12f80eea787398b0170af321878fffb5f3</originalsourceid><addsrcrecordid>eNo9kEFPGzEQRi1EBSlw44x85NAtHtu76z1GEbSRUIvacl7NOuNg2NjBdpDy71kE9DSHed87PMbOQXwH0amrgOlq_YQEEroDNgPVyEp3jTxkM6FEXYHQ5ph9zflRCNBQ6yN2rLqmM0Y2M0Z3DxRi2W-95dkmopC5X1Eo3u3538X8BjhmbpMv3uLI0Rb_giUmHh3_82t-t1xyGmNYY_ExcAwrvh7jMJElYZiEfvv2OGVfHI6Zzj7uCbu_uf63-Fnd_v6xXMxvKyuhKVWtW-OsA1lrQStt0KqhRdJtQ6idBemMIMLWtKozg4BWoFMSzLRybqidOmGX795tis87yqXf-GxpHDFQ3OVegW5BaS3lhH57R22KOSdy_Tb5DaZ9D6J_C9tPYfvPsBN-8WHeDRta_Yc_S6pXBrV2BA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3147134422</pqid></control><display><type>article</type><title>Phenotypic screens identify SCAF1 as critical activator of RNAPII elongation and global transcription</title><source>Oxford Journals Open Access Collection</source><source>DOAJ Directory of Open Access Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Bhandare, Pranjali ; Narain, Ashwin ; Hofstetter, Julia ; Rummel, Teresa ; Wenzel, Julia ; Schülein-Völk, Christina ; Lamer, Stephanie ; Eilers, Ursula ; Schlosser, Andreas ; Eilers, Martin ; Erhard, Florian ; Wolf, Elmar</creator><creatorcontrib>Bhandare, Pranjali ; Narain, Ashwin ; Hofstetter, Julia ; Rummel, Teresa ; Wenzel, Julia ; Schülein-Völk, Christina ; Lamer, Stephanie ; Eilers, Ursula ; Schlosser, Andreas ; Eilers, Martin ; Erhard, Florian ; Wolf, Elmar</creatorcontrib><description>Transcripts produced by RNA polymerase II (RNAPII) are fundamental for cellular responses to environmental changes. It is therefore no surprise that there exist multiple avenues for the regulation of this process. To explore the regulation mediated by RNAPII-interacting proteins, we used a small interfering RNA (siRNA)-based screen to systematically evaluate their influence on RNA synthesis. We identified several proteins that strongly affected RNAPII activity. We evaluated one of the top hits, SCAF1 (SR-related C-terminal domain-associated factor 1), using an auxin-inducible degradation system and sequencing approaches. In agreement with our screen results, acute depletion of SCAF1 decreased RNA synthesis, and showed an increase of Serine-2 phosphorylated-RNAPII (pS2-RNAPII). We found that the accumulation of pS2-RNAPII within the gene body occurred at GC-rich regions and was indicative of stalled RNAPII complexes. The accumulation of stalled RNAPII complexes was accompanied by reduced recruitment of initiating RNAPII, explaining the observed global decrease in transcriptional output. Furthermore, upon SCAF1 depletion, RNAPII complexes showed increased association with components of the proteasomal-degradation machinery. We concluded that in cells lacking SCAF1, RNAPII undergoes a rather interrupted passage, resulting in intervention by the proteasomal-degradation machinery to clear stalled RNAPII. While cells survive the compromised transcription caused by absence of SCAF1, further inhibition of proteasomal-degradation machinery is synthetically lethal.</description><identifier>ISSN: 0305-1048</identifier><identifier>ISSN: 1362-4962</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkae1219</identifier><identifier>PMID: 39698826</identifier><language>eng</language><publisher>England</publisher><ispartof>Nucleic acids research, 2024-12</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of Nucleic Acids Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c216t-5478fcf12540ed48ac3b7ae476ea4fc12f80eea787398b0170af321878fffb5f3</cites><orcidid>0000-0002-3574-6983 ; 0000-0002-5299-6335</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39698826$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bhandare, Pranjali</creatorcontrib><creatorcontrib>Narain, Ashwin</creatorcontrib><creatorcontrib>Hofstetter, Julia</creatorcontrib><creatorcontrib>Rummel, Teresa</creatorcontrib><creatorcontrib>Wenzel, Julia</creatorcontrib><creatorcontrib>Schülein-Völk, Christina</creatorcontrib><creatorcontrib>Lamer, Stephanie</creatorcontrib><creatorcontrib>Eilers, Ursula</creatorcontrib><creatorcontrib>Schlosser, Andreas</creatorcontrib><creatorcontrib>Eilers, Martin</creatorcontrib><creatorcontrib>Erhard, Florian</creatorcontrib><creatorcontrib>Wolf, Elmar</creatorcontrib><title>Phenotypic screens identify SCAF1 as critical activator of RNAPII elongation and global transcription</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>Transcripts produced by RNA polymerase II (RNAPII) are fundamental for cellular responses to environmental changes. It is therefore no surprise that there exist multiple avenues for the regulation of this process. To explore the regulation mediated by RNAPII-interacting proteins, we used a small interfering RNA (siRNA)-based screen to systematically evaluate their influence on RNA synthesis. We identified several proteins that strongly affected RNAPII activity. We evaluated one of the top hits, SCAF1 (SR-related C-terminal domain-associated factor 1), using an auxin-inducible degradation system and sequencing approaches. In agreement with our screen results, acute depletion of SCAF1 decreased RNA synthesis, and showed an increase of Serine-2 phosphorylated-RNAPII (pS2-RNAPII). We found that the accumulation of pS2-RNAPII within the gene body occurred at GC-rich regions and was indicative of stalled RNAPII complexes. The accumulation of stalled RNAPII complexes was accompanied by reduced recruitment of initiating RNAPII, explaining the observed global decrease in transcriptional output. Furthermore, upon SCAF1 depletion, RNAPII complexes showed increased association with components of the proteasomal-degradation machinery. We concluded that in cells lacking SCAF1, RNAPII undergoes a rather interrupted passage, resulting in intervention by the proteasomal-degradation machinery to clear stalled RNAPII. While cells survive the compromised transcription caused by absence of SCAF1, further inhibition of proteasomal-degradation machinery is synthetically lethal.</description><issn>0305-1048</issn><issn>1362-4962</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kEFPGzEQRi1EBSlw44x85NAtHtu76z1GEbSRUIvacl7NOuNg2NjBdpDy71kE9DSHed87PMbOQXwH0amrgOlq_YQEEroDNgPVyEp3jTxkM6FEXYHQ5ph9zflRCNBQ6yN2rLqmM0Y2M0Z3DxRi2W-95dkmopC5X1Eo3u3538X8BjhmbpMv3uLI0Rb_giUmHh3_82t-t1xyGmNYY_ExcAwrvh7jMJElYZiEfvv2OGVfHI6Zzj7uCbu_uf63-Fnd_v6xXMxvKyuhKVWtW-OsA1lrQStt0KqhRdJtQ6idBemMIMLWtKozg4BWoFMSzLRybqidOmGX795tis87yqXf-GxpHDFQ3OVegW5BaS3lhH57R22KOSdy_Tb5DaZ9D6J_C9tPYfvPsBN-8WHeDRta_Yc_S6pXBrV2BA</recordid><startdate>20241219</startdate><enddate>20241219</enddate><creator>Bhandare, Pranjali</creator><creator>Narain, Ashwin</creator><creator>Hofstetter, Julia</creator><creator>Rummel, Teresa</creator><creator>Wenzel, Julia</creator><creator>Schülein-Völk, Christina</creator><creator>Lamer, Stephanie</creator><creator>Eilers, Ursula</creator><creator>Schlosser, Andreas</creator><creator>Eilers, Martin</creator><creator>Erhard, Florian</creator><creator>Wolf, Elmar</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3574-6983</orcidid><orcidid>https://orcid.org/0000-0002-5299-6335</orcidid></search><sort><creationdate>20241219</creationdate><title>Phenotypic screens identify SCAF1 as critical activator of RNAPII elongation and global transcription</title><author>Bhandare, Pranjali ; Narain, Ashwin ; Hofstetter, Julia ; Rummel, Teresa ; Wenzel, Julia ; Schülein-Völk, Christina ; Lamer, Stephanie ; Eilers, Ursula ; Schlosser, Andreas ; Eilers, Martin ; Erhard, Florian ; Wolf, Elmar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c216t-5478fcf12540ed48ac3b7ae476ea4fc12f80eea787398b0170af321878fffb5f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bhandare, Pranjali</creatorcontrib><creatorcontrib>Narain, Ashwin</creatorcontrib><creatorcontrib>Hofstetter, Julia</creatorcontrib><creatorcontrib>Rummel, Teresa</creatorcontrib><creatorcontrib>Wenzel, Julia</creatorcontrib><creatorcontrib>Schülein-Völk, Christina</creatorcontrib><creatorcontrib>Lamer, Stephanie</creatorcontrib><creatorcontrib>Eilers, Ursula</creatorcontrib><creatorcontrib>Schlosser, Andreas</creatorcontrib><creatorcontrib>Eilers, Martin</creatorcontrib><creatorcontrib>Erhard, Florian</creatorcontrib><creatorcontrib>Wolf, Elmar</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bhandare, Pranjali</au><au>Narain, Ashwin</au><au>Hofstetter, Julia</au><au>Rummel, Teresa</au><au>Wenzel, Julia</au><au>Schülein-Völk, Christina</au><au>Lamer, Stephanie</au><au>Eilers, Ursula</au><au>Schlosser, Andreas</au><au>Eilers, Martin</au><au>Erhard, Florian</au><au>Wolf, Elmar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenotypic screens identify SCAF1 as critical activator of RNAPII elongation and global transcription</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2024-12-19</date><risdate>2024</risdate><issn>0305-1048</issn><issn>1362-4962</issn><eissn>1362-4962</eissn><abstract>Transcripts produced by RNA polymerase II (RNAPII) are fundamental for cellular responses to environmental changes. It is therefore no surprise that there exist multiple avenues for the regulation of this process. To explore the regulation mediated by RNAPII-interacting proteins, we used a small interfering RNA (siRNA)-based screen to systematically evaluate their influence on RNA synthesis. We identified several proteins that strongly affected RNAPII activity. We evaluated one of the top hits, SCAF1 (SR-related C-terminal domain-associated factor 1), using an auxin-inducible degradation system and sequencing approaches. In agreement with our screen results, acute depletion of SCAF1 decreased RNA synthesis, and showed an increase of Serine-2 phosphorylated-RNAPII (pS2-RNAPII). We found that the accumulation of pS2-RNAPII within the gene body occurred at GC-rich regions and was indicative of stalled RNAPII complexes. The accumulation of stalled RNAPII complexes was accompanied by reduced recruitment of initiating RNAPII, explaining the observed global decrease in transcriptional output. Furthermore, upon SCAF1 depletion, RNAPII complexes showed increased association with components of the proteasomal-degradation machinery. We concluded that in cells lacking SCAF1, RNAPII undergoes a rather interrupted passage, resulting in intervention by the proteasomal-degradation machinery to clear stalled RNAPII. While cells survive the compromised transcription caused by absence of SCAF1, further inhibition of proteasomal-degradation machinery is synthetically lethal.</abstract><cop>England</cop><pmid>39698826</pmid><doi>10.1093/nar/gkae1219</doi><orcidid>https://orcid.org/0000-0002-3574-6983</orcidid><orcidid>https://orcid.org/0000-0002-5299-6335</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0305-1048 |
ispartof | Nucleic acids research, 2024-12 |
issn | 0305-1048 1362-4962 1362-4962 |
language | eng |
recordid | cdi_proquest_miscellaneous_3147134422 |
source | Oxford Journals Open Access Collection; DOAJ Directory of Open Access Journals; PubMed Central; Free Full-Text Journals in Chemistry |
title | Phenotypic screens identify SCAF1 as critical activator of RNAPII elongation and global transcription |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T00%3A01%3A48IST&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=Phenotypic%20screens%20identify%20SCAF1%20as%20critical%20activator%20of%20RNAPII%20elongation%20and%20global%20transcription&rft.jtitle=Nucleic%20acids%20research&rft.au=Bhandare,%20Pranjali&rft.date=2024-12-19&rft.issn=0305-1048&rft.eissn=1362-4962&rft_id=info:doi/10.1093/nar/gkae1219&rft_dat=%3Cproquest_cross%3E3147134422%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=3147134422&rft_id=info:pmid/39698826&rfr_iscdi=true |