Group II intron-like reverse transcriptases function in double-strand break repair
Bacteria encode reverse transcriptases (RTs) of unknown function that are closely related to group II intron-encoded RTs. We found that a Pseudomonas aeruginosa group II intron-like RT (G2L4 RT) with YIDD instead of YADD at its active site functions in DNA repair in its native host and when expresse...
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Veröffentlicht in: | Cell 2022-09, Vol.185 (20), p.3671-3688.e23 |
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creator | Park, Seung Kuk Mohr, Georg Yao, Jun Russell, Rick Lambowitz, Alan M |
description | Bacteria encode reverse transcriptases (RTs) of unknown function that are closely related to group II intron-encoded RTs. We found that a Pseudomonas aeruginosa group II intron-like RT (G2L4 RT) with YIDD instead of YADD at its active site functions in DNA repair in its native host and when expressed in Escherichia coli. G2L4 RT has biochemical activities strikingly similar to those of human DNA repair polymerase θ and uses them for translesion DNA synthesis and double-strand break repair (DSBR) via microhomology-mediated end-joining (MMEJ). We also found that a group II intron RT can function similarly in DNA repair, with reciprocal active-site substitutions showing isoleucine favors MMEJ and alanine favors primer extension in both enzymes. These DNA repair functions utilize conserved structural features of non-LTR-retroelement RTs, including human LINE-1 and other eukaryotic non-LTR-retrotransposon RTs, suggesting such enzymes may have inherent ability to function in DSBR in a wide range of organisms. |
doi_str_mv | 10.1016/j.cell.2022.08.014 |
format | Article |
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We found that a Pseudomonas aeruginosa group II intron-like RT (G2L4 RT) with YIDD instead of YADD at its active site functions in DNA repair in its native host and when expressed in Escherichia coli. G2L4 RT has biochemical activities strikingly similar to those of human DNA repair polymerase θ and uses them for translesion DNA synthesis and double-strand break repair (DSBR) via microhomology-mediated end-joining (MMEJ). We also found that a group II intron RT can function similarly in DNA repair, with reciprocal active-site substitutions showing isoleucine favors MMEJ and alanine favors primer extension in both enzymes. These DNA repair functions utilize conserved structural features of non-LTR-retroelement RTs, including human LINE-1 and other eukaryotic non-LTR-retrotransposon RTs, suggesting such enzymes may have inherent ability to function in DSBR in a wide range of organisms.</description><identifier>ISSN: 0092-8674</identifier><identifier>EISSN: 1097-4172</identifier><identifier>DOI: 10.1016/j.cell.2022.08.014</identifier><identifier>PMID: 36113466</identifier><language>eng</language><publisher>United States</publisher><subject>Alanine - genetics ; DNA End-Joining Repair ; DNA Repair ; DNA-Directed RNA Polymerases - genetics ; Humans ; Introns ; Isoleucine - genetics ; Retroelements ; RNA-Directed DNA Polymerase - chemistry</subject><ispartof>Cell, 2022-09, Vol.185 (20), p.3671-3688.e23</ispartof><rights>Copyright © 2022 Elsevier Inc. 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We found that a Pseudomonas aeruginosa group II intron-like RT (G2L4 RT) with YIDD instead of YADD at its active site functions in DNA repair in its native host and when expressed in Escherichia coli. G2L4 RT has biochemical activities strikingly similar to those of human DNA repair polymerase θ and uses them for translesion DNA synthesis and double-strand break repair (DSBR) via microhomology-mediated end-joining (MMEJ). We also found that a group II intron RT can function similarly in DNA repair, with reciprocal active-site substitutions showing isoleucine favors MMEJ and alanine favors primer extension in both enzymes. These DNA repair functions utilize conserved structural features of non-LTR-retroelement RTs, including human LINE-1 and other eukaryotic non-LTR-retrotransposon RTs, suggesting such enzymes may have inherent ability to function in DSBR in a wide range of organisms.</description><subject>Alanine - genetics</subject><subject>DNA End-Joining Repair</subject><subject>DNA Repair</subject><subject>DNA-Directed RNA Polymerases - genetics</subject><subject>Humans</subject><subject>Introns</subject><subject>Isoleucine - genetics</subject><subject>Retroelements</subject><subject>RNA-Directed DNA Polymerase - chemistry</subject><issn>0092-8674</issn><issn>1097-4172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUctK7TAUDXJFj48fcCAd3klrnm0yuXARHwcEQXQcknRXc-xpatIK_r0pPtDRHuy11t5rLYROCK4IJvXZpnLQ9xXFlFZYVpjwHbQiWDUlJw39g1YYK1rKuuH76CClDcZYCiH20D6rCWG8rlfo7iqGeSzW68IPUwxD2ftnKCK8QkxQTNEMyUU_TiZBKrp5cJMPQ8YWbZhtD2VaIG1hI5jnTBuNj0dotzN9guPPeYgeLi_uz6_Lm9ur9fn_m9JxTKdSMldLKpXhQlpSU9VIYmknnMBUAVeWqbbmJttRHReqFVaBYLZtrBPAoGWH6N-H7jjbLbQOsgHT6zH6rYlvOhivf28G_6Qfw6tWguUoeBb4-ykQw8sMadJbn5ZIzQBhTpo2RHCOBaUZSj-gLoaUInTfZwjWSxl6oxemXsrQWOpcRiad_nzwm_KVPnsHexqILw</recordid><startdate>20220929</startdate><enddate>20220929</enddate><creator>Park, Seung Kuk</creator><creator>Mohr, Georg</creator><creator>Yao, Jun</creator><creator>Russell, Rick</creator><creator>Lambowitz, Alan M</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><scope>5PM</scope></search><sort><creationdate>20220929</creationdate><title>Group II intron-like reverse transcriptases function in double-strand break repair</title><author>Park, Seung Kuk ; Mohr, Georg ; Yao, Jun ; Russell, Rick ; Lambowitz, Alan M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-83c68289a458b1629781b2f5c5029e49b39d64a0979f459d5b9e53bd7bc5e3ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alanine - genetics</topic><topic>DNA End-Joining Repair</topic><topic>DNA Repair</topic><topic>DNA-Directed RNA Polymerases - genetics</topic><topic>Humans</topic><topic>Introns</topic><topic>Isoleucine - genetics</topic><topic>Retroelements</topic><topic>RNA-Directed DNA Polymerase - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Seung Kuk</creatorcontrib><creatorcontrib>Mohr, Georg</creatorcontrib><creatorcontrib>Yao, Jun</creatorcontrib><creatorcontrib>Russell, Rick</creatorcontrib><creatorcontrib>Lambowitz, Alan M</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Seung Kuk</au><au>Mohr, Georg</au><au>Yao, Jun</au><au>Russell, Rick</au><au>Lambowitz, Alan M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Group II intron-like reverse transcriptases function in double-strand break repair</atitle><jtitle>Cell</jtitle><addtitle>Cell</addtitle><date>2022-09-29</date><risdate>2022</risdate><volume>185</volume><issue>20</issue><spage>3671</spage><epage>3688.e23</epage><pages>3671-3688.e23</pages><issn>0092-8674</issn><eissn>1097-4172</eissn><abstract>Bacteria encode reverse transcriptases (RTs) of unknown function that are closely related to group II intron-encoded RTs. We found that a Pseudomonas aeruginosa group II intron-like RT (G2L4 RT) with YIDD instead of YADD at its active site functions in DNA repair in its native host and when expressed in Escherichia coli. G2L4 RT has biochemical activities strikingly similar to those of human DNA repair polymerase θ and uses them for translesion DNA synthesis and double-strand break repair (DSBR) via microhomology-mediated end-joining (MMEJ). We also found that a group II intron RT can function similarly in DNA repair, with reciprocal active-site substitutions showing isoleucine favors MMEJ and alanine favors primer extension in both enzymes. These DNA repair functions utilize conserved structural features of non-LTR-retroelement RTs, including human LINE-1 and other eukaryotic non-LTR-retrotransposon RTs, suggesting such enzymes may have inherent ability to function in DSBR in a wide range of organisms.</abstract><cop>United States</cop><pmid>36113466</pmid><doi>10.1016/j.cell.2022.08.014</doi><oa>free_for_read</oa></addata></record> |
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source | Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE; Cell Press Free Archives; EZB-FREE-00999 freely available EZB journals |
subjects | Alanine - genetics DNA End-Joining Repair DNA Repair DNA-Directed RNA Polymerases - genetics Humans Introns Isoleucine - genetics Retroelements RNA-Directed DNA Polymerase - chemistry |
title | Group II intron-like reverse transcriptases function in double-strand break repair |
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