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Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro
Abstract Pseudouridine (Ψ) at position 55 in tRNAs plays an important role in their structure and function. This modification is catalyzed by TruB/Pus4/Cbf5 family of pseudouridine synthases in bacteria and yeast. However, the mechanism of TRUB family underlying the formation of Ψ55 in the mammalian...
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Published in: | Nucleic acids research 2022-09, Vol.50 (16), p.9368-9381 |
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description | Abstract
Pseudouridine (Ψ) at position 55 in tRNAs plays an important role in their structure and function. This modification is catalyzed by TruB/Pus4/Cbf5 family of pseudouridine synthases in bacteria and yeast. However, the mechanism of TRUB family underlying the formation of Ψ55 in the mammalian tRNAs is largely unknown. In this report, the CMC/reverse transcription assays demonstrated the presence of Ψ55 in the human mitochondrial tRNAAsn, tRNAGln, tRNAGlu, tRNAPro, tRNAMet, tRNALeu(UUR) and tRNASer(UCN). TRUB1 knockout (KO) cell lines generated by CRISPR/Cas9 technology exhibited the loss of Ψ55 modification in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro but did not affect other 18 mitochondrial tRNAs. An in vitro assay revealed that recombinant TRUB1 protein can catalyze the efficient formation of Ψ55 in tRNAAsn and tRNAGln, but not in tRNAMet and tRNAArg. Notably, the overexpression of TRUB1 cDNA reversed the deficient Ψ55 modifications in these tRNAs in TRUB1KO HeLa cells. TRUB1 deficiency affected the base-pairing (18A/G-Ψ55), conformation and stability but not aminoacylation capacity of these tRNAs. Furthermore, TRUB1 deficiency impacted mitochondrial translation and biogenesis of oxidative phosphorylation system. Our findings demonstrated that human TRUB1 is a highly conserved mitochondrial pseudouridine synthase responsible for the Ψ55 modification in the mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro. |
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Pseudouridine (Ψ) at position 55 in tRNAs plays an important role in their structure and function. This modification is catalyzed by TruB/Pus4/Cbf5 family of pseudouridine synthases in bacteria and yeast. However, the mechanism of TRUB family underlying the formation of Ψ55 in the mammalian tRNAs is largely unknown. In this report, the CMC/reverse transcription assays demonstrated the presence of Ψ55 in the human mitochondrial tRNAAsn, tRNAGln, tRNAGlu, tRNAPro, tRNAMet, tRNALeu(UUR) and tRNASer(UCN). TRUB1 knockout (KO) cell lines generated by CRISPR/Cas9 technology exhibited the loss of Ψ55 modification in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro but did not affect other 18 mitochondrial tRNAs. An in vitro assay revealed that recombinant TRUB1 protein can catalyze the efficient formation of Ψ55 in tRNAAsn and tRNAGln, but not in tRNAMet and tRNAArg. Notably, the overexpression of TRUB1 cDNA reversed the deficient Ψ55 modifications in these tRNAs in TRUB1KO HeLa cells. TRUB1 deficiency affected the base-pairing (18A/G-Ψ55), conformation and stability but not aminoacylation capacity of these tRNAs. Furthermore, TRUB1 deficiency impacted mitochondrial translation and biogenesis of oxidative phosphorylation system. Our findings demonstrated that human TRUB1 is a highly conserved mitochondrial pseudouridine synthase responsible for the Ψ55 modification in the mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkac698</identifier><identifier>PMID: 36018806</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Animals ; HeLa Cells ; Humans ; Intramolecular Transferases - genetics ; Intramolecular Transferases - metabolism ; Mammals - genetics ; Pseudouridine - genetics ; Pseudouridine - metabolism ; RNA and RNA-protein complexes ; RNA, Transfer - metabolism ; RNA, Transfer, Asn ; RNA, Transfer, Gln ; RNA, Transfer, Glu ; RNA, Transfer, Met ; RNA, Transfer, Pro</subject><ispartof>Nucleic acids research, 2022-09, Vol.50 (16), p.9368-9381</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. 2022</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c342t-ecd7f1928edc14cdaaa31f4f412678628c0fe0984cfe75b0071a5114ca537b8c3</citedby><cites>FETCH-LOGICAL-c342t-ecd7f1928edc14cdaaa31f4f412678628c0fe0984cfe75b0071a5114ca537b8c3</cites><orcidid>0000-0003-0340-6180 ; 0000-0003-1272-069X ; 0000-0001-5067-6736 ; 0000-0003-3182-593X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458420/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458420/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1598,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36018806$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jia, Zidong</creatorcontrib><creatorcontrib>Meng, Feilong</creatorcontrib><creatorcontrib>Chen, Hui</creatorcontrib><creatorcontrib>Zhu, Gao</creatorcontrib><creatorcontrib>Li, Xincheng</creatorcontrib><creatorcontrib>He, Yunfan</creatorcontrib><creatorcontrib>Zhang, Liyao</creatorcontrib><creatorcontrib>He, Xiao</creatorcontrib><creatorcontrib>Zhan, Huisen</creatorcontrib><creatorcontrib>Chen, Mengquan</creatorcontrib><creatorcontrib>Ji, Yanchun</creatorcontrib><creatorcontrib>Wang, Meng</creatorcontrib><creatorcontrib>Guan, Min-Xin</creatorcontrib><title>Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>Abstract
Pseudouridine (Ψ) at position 55 in tRNAs plays an important role in their structure and function. This modification is catalyzed by TruB/Pus4/Cbf5 family of pseudouridine synthases in bacteria and yeast. However, the mechanism of TRUB family underlying the formation of Ψ55 in the mammalian tRNAs is largely unknown. In this report, the CMC/reverse transcription assays demonstrated the presence of Ψ55 in the human mitochondrial tRNAAsn, tRNAGln, tRNAGlu, tRNAPro, tRNAMet, tRNALeu(UUR) and tRNASer(UCN). TRUB1 knockout (KO) cell lines generated by CRISPR/Cas9 technology exhibited the loss of Ψ55 modification in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro but did not affect other 18 mitochondrial tRNAs. An in vitro assay revealed that recombinant TRUB1 protein can catalyze the efficient formation of Ψ55 in tRNAAsn and tRNAGln, but not in tRNAMet and tRNAArg. Notably, the overexpression of TRUB1 cDNA reversed the deficient Ψ55 modifications in these tRNAs in TRUB1KO HeLa cells. TRUB1 deficiency affected the base-pairing (18A/G-Ψ55), conformation and stability but not aminoacylation capacity of these tRNAs. Furthermore, TRUB1 deficiency impacted mitochondrial translation and biogenesis of oxidative phosphorylation system. Our findings demonstrated that human TRUB1 is a highly conserved mitochondrial pseudouridine synthase responsible for the Ψ55 modification in the mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro.</description><subject>Animals</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Intramolecular Transferases - genetics</subject><subject>Intramolecular Transferases - metabolism</subject><subject>Mammals - genetics</subject><subject>Pseudouridine - genetics</subject><subject>Pseudouridine - metabolism</subject><subject>RNA and RNA-protein complexes</subject><subject>RNA, Transfer - metabolism</subject><subject>RNA, Transfer, Asn</subject><subject>RNA, Transfer, Gln</subject><subject>RNA, Transfer, Glu</subject><subject>RNA, Transfer, Met</subject><subject>RNA, Transfer, Pro</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kcFu1DAQhi1ERZfCiTvyCSFBWjuxE-eCtFTQVqoAVe3ZmnXGG0NiBzuptA_CO_A0PBNhd1mVC6f5pfn0zUg_IS84O-WsLs48xLP1NzBlrR6RBS_KPBN1mT8mC1YwmXEm1DF5mtJXxrjgUjwhx0XJuFKsXJAfl1MPnt7e3L3n1CUKtHXrtttQE3zCeI8NHRJOTZiia5xHmjZ-bCEhjZiGmXGrDqkNkY7tdvYwuuBpsPTXTymp87R3YzBt8E100NHx5tNymfzbbbjoDmGi4Jtt_hLDM3JkoUv4fD9PyN3HD7fnl9n154ur8-V1ZgqRjxmaprK8zhU2hgvTAEDBrbCC52WlylwZZpHVShiLlVwxVnGQfCZBFtVKmeKEvNt5h2nVzxL0Y4ROD9H1EDc6gNP_brxr9Trc61pIJXI2C17vBTF8nzCNunfJYNeBxzAlnVesKrmsmZrRNzvUxJBSRHs4w5n-U6Sei9T7Imf65cPPDuzf5mbg1Q4I0_Bf0287e6qF</recordid><startdate>20220909</startdate><enddate>20220909</enddate><creator>Jia, Zidong</creator><creator>Meng, Feilong</creator><creator>Chen, Hui</creator><creator>Zhu, Gao</creator><creator>Li, Xincheng</creator><creator>He, Yunfan</creator><creator>Zhang, Liyao</creator><creator>He, Xiao</creator><creator>Zhan, Huisen</creator><creator>Chen, Mengquan</creator><creator>Ji, Yanchun</creator><creator>Wang, Meng</creator><creator>Guan, Min-Xin</creator><general>Oxford University Press</general><scope>TOX</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0340-6180</orcidid><orcidid>https://orcid.org/0000-0003-1272-069X</orcidid><orcidid>https://orcid.org/0000-0001-5067-6736</orcidid><orcidid>https://orcid.org/0000-0003-3182-593X</orcidid></search><sort><creationdate>20220909</creationdate><title>Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro</title><author>Jia, Zidong ; Meng, Feilong ; Chen, Hui ; Zhu, Gao ; Li, Xincheng ; He, Yunfan ; Zhang, Liyao ; He, Xiao ; Zhan, Huisen ; Chen, Mengquan ; Ji, Yanchun ; Wang, Meng ; Guan, Min-Xin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c342t-ecd7f1928edc14cdaaa31f4f412678628c0fe0984cfe75b0071a5114ca537b8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Intramolecular Transferases - genetics</topic><topic>Intramolecular Transferases - metabolism</topic><topic>Mammals - genetics</topic><topic>Pseudouridine - genetics</topic><topic>Pseudouridine - metabolism</topic><topic>RNA and RNA-protein complexes</topic><topic>RNA, Transfer - metabolism</topic><topic>RNA, Transfer, Asn</topic><topic>RNA, Transfer, Gln</topic><topic>RNA, Transfer, Glu</topic><topic>RNA, Transfer, Met</topic><topic>RNA, Transfer, Pro</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jia, Zidong</creatorcontrib><creatorcontrib>Meng, Feilong</creatorcontrib><creatorcontrib>Chen, Hui</creatorcontrib><creatorcontrib>Zhu, Gao</creatorcontrib><creatorcontrib>Li, Xincheng</creatorcontrib><creatorcontrib>He, Yunfan</creatorcontrib><creatorcontrib>Zhang, Liyao</creatorcontrib><creatorcontrib>He, Xiao</creatorcontrib><creatorcontrib>Zhan, Huisen</creatorcontrib><creatorcontrib>Chen, Mengquan</creatorcontrib><creatorcontrib>Ji, Yanchun</creatorcontrib><creatorcontrib>Wang, Meng</creatorcontrib><creatorcontrib>Guan, Min-Xin</creatorcontrib><collection>Oxford Open</collection><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>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jia, Zidong</au><au>Meng, Feilong</au><au>Chen, Hui</au><au>Zhu, Gao</au><au>Li, Xincheng</au><au>He, Yunfan</au><au>Zhang, Liyao</au><au>He, Xiao</au><au>Zhan, Huisen</au><au>Chen, Mengquan</au><au>Ji, Yanchun</au><au>Wang, Meng</au><au>Guan, Min-Xin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2022-09-09</date><risdate>2022</risdate><volume>50</volume><issue>16</issue><spage>9368</spage><epage>9381</epage><pages>9368-9381</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>Abstract
Pseudouridine (Ψ) at position 55 in tRNAs plays an important role in their structure and function. This modification is catalyzed by TruB/Pus4/Cbf5 family of pseudouridine synthases in bacteria and yeast. However, the mechanism of TRUB family underlying the formation of Ψ55 in the mammalian tRNAs is largely unknown. In this report, the CMC/reverse transcription assays demonstrated the presence of Ψ55 in the human mitochondrial tRNAAsn, tRNAGln, tRNAGlu, tRNAPro, tRNAMet, tRNALeu(UUR) and tRNASer(UCN). TRUB1 knockout (KO) cell lines generated by CRISPR/Cas9 technology exhibited the loss of Ψ55 modification in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro but did not affect other 18 mitochondrial tRNAs. An in vitro assay revealed that recombinant TRUB1 protein can catalyze the efficient formation of Ψ55 in tRNAAsn and tRNAGln, but not in tRNAMet and tRNAArg. Notably, the overexpression of TRUB1 cDNA reversed the deficient Ψ55 modifications in these tRNAs in TRUB1KO HeLa cells. TRUB1 deficiency affected the base-pairing (18A/G-Ψ55), conformation and stability but not aminoacylation capacity of these tRNAs. Furthermore, TRUB1 deficiency impacted mitochondrial translation and biogenesis of oxidative phosphorylation system. Our findings demonstrated that human TRUB1 is a highly conserved mitochondrial pseudouridine synthase responsible for the Ψ55 modification in the mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>36018806</pmid><doi>10.1093/nar/gkac698</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-0340-6180</orcidid><orcidid>https://orcid.org/0000-0003-1272-069X</orcidid><orcidid>https://orcid.org/0000-0001-5067-6736</orcidid><orcidid>https://orcid.org/0000-0003-3182-593X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals HeLa Cells Humans Intramolecular Transferases - genetics Intramolecular Transferases - metabolism Mammals - genetics Pseudouridine - genetics Pseudouridine - metabolism RNA and RNA-protein complexes RNA, Transfer - metabolism RNA, Transfer, Asn RNA, Transfer, Gln RNA, Transfer, Glu RNA, Transfer, Met RNA, Transfer, Pro |
title | Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro |
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