The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs

Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is requi...
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Autor*in:	Stefanie Gerstberger [verfasserIn] Cindy Meyer [verfasserIn] Sigi Benjamin-Hong [verfasserIn] Joe Rodriguez [verfasserIn] Daniel Briskin [verfasserIn] Claudia Bognanni [verfasserIn] Kimberly Bogardus [verfasserIn] Hermann Steller [verfasserIn] Thomas Tuschl [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2017

Schlagwörter:	rRNA biogenesis rRNA 3′ end maturation rRNA processing snoRNA biogenesis snoRNA 3′ end maturation snoRNA processing RNA exonuclease U8 snoRNA

Übergeordnetes Werk:	In: Cell Reports - Elsevier, 2015, 21(2017), 3, Seite 758-772
Übergeordnetes Werk:	volume:21 ; year:2017 ; number:3 ; pages:758-772

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.1016/j.celrep.2017.09.067

Katalog-ID:	DOAJ012661481

Internformat


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520			\|a Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is required for small nucleolar RNA (snoRNA) and rRNA biogenesis and is essential in D. melanogaster. Loss-of-function mutants accumulate improperly 3′ end-trimmed 28S rRNA, 5S rRNA, and snoRNA precursors in vivo. Rexo5 is ubiquitously expressed at low levels in somatic metazoan cells but extremely elevated in male and female germ cells. Loss of Rexo5 leads to increased nucleolar size, genomic instability, defective ribosome subunit export, and larval death. Loss of germline expression compromises gonadal growth and meiotic entry during germline development.
650		4	\|a rRNA biogenesis
650		4	\|a rRNA 3′ end maturation
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650		4	\|a snoRNA biogenesis
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650		4	\|a snoRNA processing
650		4	\|a RNA exonuclease
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700	0		\|a Kimberly Bogardus \|e verfasserin \|4 aut
700	0		\|a Hermann Steller \|e verfasserin \|4 aut
700	0		\|a Thomas Tuschl \|e verfasserin \|4 aut
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912			\|a GBV_ILN_4393
912			\|a GBV_ILN_4700
951			\|a AR
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allfields	10.1016/j.celrep.2017.09.067 doi (DE-627)DOAJ012661481 (DE-599)DOAJ06c6c57008cb4839b64703f881b49613 DE-627 ger DE-627 rakwb eng QH301-705.5 Stefanie Gerstberger verfasserin aut The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is required for small nucleolar RNA (snoRNA) and rRNA biogenesis and is essential in D. melanogaster. Loss-of-function mutants accumulate improperly 3′ end-trimmed 28S rRNA, 5S rRNA, and snoRNA precursors in vivo. Rexo5 is ubiquitously expressed at low levels in somatic metazoan cells but extremely elevated in male and female germ cells. Loss of Rexo5 leads to increased nucleolar size, genomic instability, defective ribosome subunit export, and larval death. Loss of germline expression compromises gonadal growth and meiotic entry during germline development. rRNA biogenesis rRNA 3′ end maturation rRNA processing snoRNA biogenesis snoRNA 3′ end maturation snoRNA processing RNA exonuclease U8 snoRNA Biology (General) Cindy Meyer verfasserin aut Sigi Benjamin-Hong verfasserin aut Joe Rodriguez verfasserin aut Daniel Briskin verfasserin aut Claudia Bognanni verfasserin aut Kimberly Bogardus verfasserin aut Hermann Steller verfasserin aut Thomas Tuschl verfasserin aut In Cell Reports Elsevier, 2015 21(2017), 3, Seite 758-772 (DE-627)684964562 (DE-600)2649101-1 22111247 nnns volume:21 year:2017 number:3 pages:758-772 https://doi.org/10.1016/j.celrep.2017.09.067 kostenfrei https://doaj.org/article/06c6c57008cb4839b64703f881b49613 kostenfrei http://www.sciencedirect.com/science/article/pii/S2211124717313724 kostenfrei https://doaj.org/toc/2211-1247 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 21 2017 3 758-772
spelling	10.1016/j.celrep.2017.09.067 doi (DE-627)DOAJ012661481 (DE-599)DOAJ06c6c57008cb4839b64703f881b49613 DE-627 ger DE-627 rakwb eng QH301-705.5 Stefanie Gerstberger verfasserin aut The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is required for small nucleolar RNA (snoRNA) and rRNA biogenesis and is essential in D. melanogaster. Loss-of-function mutants accumulate improperly 3′ end-trimmed 28S rRNA, 5S rRNA, and snoRNA precursors in vivo. Rexo5 is ubiquitously expressed at low levels in somatic metazoan cells but extremely elevated in male and female germ cells. Loss of Rexo5 leads to increased nucleolar size, genomic instability, defective ribosome subunit export, and larval death. Loss of germline expression compromises gonadal growth and meiotic entry during germline development. rRNA biogenesis rRNA 3′ end maturation rRNA processing snoRNA biogenesis snoRNA 3′ end maturation snoRNA processing RNA exonuclease U8 snoRNA Biology (General) Cindy Meyer verfasserin aut Sigi Benjamin-Hong verfasserin aut Joe Rodriguez verfasserin aut Daniel Briskin verfasserin aut Claudia Bognanni verfasserin aut Kimberly Bogardus verfasserin aut Hermann Steller verfasserin aut Thomas Tuschl verfasserin aut In Cell Reports Elsevier, 2015 21(2017), 3, Seite 758-772 (DE-627)684964562 (DE-600)2649101-1 22111247 nnns volume:21 year:2017 number:3 pages:758-772 https://doi.org/10.1016/j.celrep.2017.09.067 kostenfrei https://doaj.org/article/06c6c57008cb4839b64703f881b49613 kostenfrei http://www.sciencedirect.com/science/article/pii/S2211124717313724 kostenfrei https://doaj.org/toc/2211-1247 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 21 2017 3 758-772
allfields_unstemmed	10.1016/j.celrep.2017.09.067 doi (DE-627)DOAJ012661481 (DE-599)DOAJ06c6c57008cb4839b64703f881b49613 DE-627 ger DE-627 rakwb eng QH301-705.5 Stefanie Gerstberger verfasserin aut The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is required for small nucleolar RNA (snoRNA) and rRNA biogenesis and is essential in D. melanogaster. Loss-of-function mutants accumulate improperly 3′ end-trimmed 28S rRNA, 5S rRNA, and snoRNA precursors in vivo. Rexo5 is ubiquitously expressed at low levels in somatic metazoan cells but extremely elevated in male and female germ cells. Loss of Rexo5 leads to increased nucleolar size, genomic instability, defective ribosome subunit export, and larval death. Loss of germline expression compromises gonadal growth and meiotic entry during germline development. rRNA biogenesis rRNA 3′ end maturation rRNA processing snoRNA biogenesis snoRNA 3′ end maturation snoRNA processing RNA exonuclease U8 snoRNA Biology (General) Cindy Meyer verfasserin aut Sigi Benjamin-Hong verfasserin aut Joe Rodriguez verfasserin aut Daniel Briskin verfasserin aut Claudia Bognanni verfasserin aut Kimberly Bogardus verfasserin aut Hermann Steller verfasserin aut Thomas Tuschl verfasserin aut In Cell Reports Elsevier, 2015 21(2017), 3, Seite 758-772 (DE-627)684964562 (DE-600)2649101-1 22111247 nnns volume:21 year:2017 number:3 pages:758-772 https://doi.org/10.1016/j.celrep.2017.09.067 kostenfrei https://doaj.org/article/06c6c57008cb4839b64703f881b49613 kostenfrei http://www.sciencedirect.com/science/article/pii/S2211124717313724 kostenfrei https://doaj.org/toc/2211-1247 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 21 2017 3 758-772
allfieldsGer	10.1016/j.celrep.2017.09.067 doi (DE-627)DOAJ012661481 (DE-599)DOAJ06c6c57008cb4839b64703f881b49613 DE-627 ger DE-627 rakwb eng QH301-705.5 Stefanie Gerstberger verfasserin aut The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is required for small nucleolar RNA (snoRNA) and rRNA biogenesis and is essential in D. melanogaster. Loss-of-function mutants accumulate improperly 3′ end-trimmed 28S rRNA, 5S rRNA, and snoRNA precursors in vivo. Rexo5 is ubiquitously expressed at low levels in somatic metazoan cells but extremely elevated in male and female germ cells. Loss of Rexo5 leads to increased nucleolar size, genomic instability, defective ribosome subunit export, and larval death. Loss of germline expression compromises gonadal growth and meiotic entry during germline development. rRNA biogenesis rRNA 3′ end maturation rRNA processing snoRNA biogenesis snoRNA 3′ end maturation snoRNA processing RNA exonuclease U8 snoRNA Biology (General) Cindy Meyer verfasserin aut Sigi Benjamin-Hong verfasserin aut Joe Rodriguez verfasserin aut Daniel Briskin verfasserin aut Claudia Bognanni verfasserin aut Kimberly Bogardus verfasserin aut Hermann Steller verfasserin aut Thomas Tuschl verfasserin aut In Cell Reports Elsevier, 2015 21(2017), 3, Seite 758-772 (DE-627)684964562 (DE-600)2649101-1 22111247 nnns volume:21 year:2017 number:3 pages:758-772 https://doi.org/10.1016/j.celrep.2017.09.067 kostenfrei https://doaj.org/article/06c6c57008cb4839b64703f881b49613 kostenfrei http://www.sciencedirect.com/science/article/pii/S2211124717313724 kostenfrei https://doaj.org/toc/2211-1247 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 21 2017 3 758-772
allfieldsSound	10.1016/j.celrep.2017.09.067 doi (DE-627)DOAJ012661481 (DE-599)DOAJ06c6c57008cb4839b64703f881b49613 DE-627 ger DE-627 rakwb eng QH301-705.5 Stefanie Gerstberger verfasserin aut The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs 2017 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is required for small nucleolar RNA (snoRNA) and rRNA biogenesis and is essential in D. melanogaster. Loss-of-function mutants accumulate improperly 3′ end-trimmed 28S rRNA, 5S rRNA, and snoRNA precursors in vivo. Rexo5 is ubiquitously expressed at low levels in somatic metazoan cells but extremely elevated in male and female germ cells. Loss of Rexo5 leads to increased nucleolar size, genomic instability, defective ribosome subunit export, and larval death. Loss of germline expression compromises gonadal growth and meiotic entry during germline development. rRNA biogenesis rRNA 3′ end maturation rRNA processing snoRNA biogenesis snoRNA 3′ end maturation snoRNA processing RNA exonuclease U8 snoRNA Biology (General) Cindy Meyer verfasserin aut Sigi Benjamin-Hong verfasserin aut Joe Rodriguez verfasserin aut Daniel Briskin verfasserin aut Claudia Bognanni verfasserin aut Kimberly Bogardus verfasserin aut Hermann Steller verfasserin aut Thomas Tuschl verfasserin aut In Cell Reports Elsevier, 2015 21(2017), 3, Seite 758-772 (DE-627)684964562 (DE-600)2649101-1 22111247 nnns volume:21 year:2017 number:3 pages:758-772 https://doi.org/10.1016/j.celrep.2017.09.067 kostenfrei https://doaj.org/article/06c6c57008cb4839b64703f881b49613 kostenfrei http://www.sciencedirect.com/science/article/pii/S2211124717313724 kostenfrei https://doaj.org/toc/2211-1247 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2110 GBV_ILN_2112 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 21 2017 3 758-772
language	English
source	In Cell Reports 21(2017), 3, Seite 758-772 volume:21 year:2017 number:3 pages:758-772
sourceStr	In Cell Reports 21(2017), 3, Seite 758-772 volume:21 year:2017 number:3 pages:758-772
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	rRNA biogenesis rRNA 3′ end maturation rRNA processing snoRNA biogenesis snoRNA 3′ end maturation snoRNA processing RNA exonuclease U8 snoRNA Biology (General)
isfreeaccess_bool	true
container_title	Cell Reports
authorswithroles_txt_mv	Stefanie Gerstberger @@aut@@ Cindy Meyer @@aut@@ Sigi Benjamin-Hong @@aut@@ Joe Rodriguez @@aut@@ Daniel Briskin @@aut@@ Claudia Bognanni @@aut@@ Kimberly Bogardus @@aut@@ Hermann Steller @@aut@@ Thomas Tuschl @@aut@@
publishDateDaySort_date	2017-01-01T00:00:00Z
hierarchy_top_id	684964562
id	DOAJ012661481
language_de	englisch
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callnumber-first	Q - Science
author	Stefanie Gerstberger
spellingShingle	Stefanie Gerstberger misc QH301-705.5 misc rRNA biogenesis misc rRNA 3′ end maturation misc rRNA processing misc snoRNA biogenesis misc snoRNA 3′ end maturation misc snoRNA processing misc RNA exonuclease misc U8 snoRNA misc Biology (General) The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs
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topic_title	QH301-705.5 The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs rRNA biogenesis rRNA 3′ end maturation rRNA processing snoRNA biogenesis snoRNA 3′ end maturation snoRNA processing RNA exonuclease U8 snoRNA
topic	misc QH301-705.5 misc rRNA biogenesis misc rRNA 3′ end maturation misc rRNA processing misc snoRNA biogenesis misc snoRNA 3′ end maturation misc snoRNA processing misc RNA exonuclease misc U8 snoRNA misc Biology (General)
topic_unstemmed	misc QH301-705.5 misc rRNA biogenesis misc rRNA 3′ end maturation misc rRNA processing misc snoRNA biogenesis misc snoRNA 3′ end maturation misc snoRNA processing misc RNA exonuclease misc U8 snoRNA misc Biology (General)
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title	The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs
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title_full	The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs
author_sort	Stefanie Gerstberger
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author_browse	Stefanie Gerstberger Cindy Meyer Sigi Benjamin-Hong Joe Rodriguez Daniel Briskin Claudia Bognanni Kimberly Bogardus Hermann Steller Thomas Tuschl
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author-letter	Stefanie Gerstberger
doi_str_mv	10.1016/j.celrep.2017.09.067
author2-role	verfasserin
title_sort	conserved rna exonuclease rexo5 is required for 3′ end maturation of 28s rrna, 5s rrna, and snornas
callnumber	QH301-705.5
title_auth	The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs
abstract	Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is required for small nucleolar RNA (snoRNA) and rRNA biogenesis and is essential in D. melanogaster. Loss-of-function mutants accumulate improperly 3′ end-trimmed 28S rRNA, 5S rRNA, and snoRNA precursors in vivo. Rexo5 is ubiquitously expressed at low levels in somatic metazoan cells but extremely elevated in male and female germ cells. Loss of Rexo5 leads to increased nucleolar size, genomic instability, defective ribosome subunit export, and larval death. Loss of germline expression compromises gonadal growth and meiotic entry during germline development.
abstractGer	Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is required for small nucleolar RNA (snoRNA) and rRNA biogenesis and is essential in D. melanogaster. Loss-of-function mutants accumulate improperly 3′ end-trimmed 28S rRNA, 5S rRNA, and snoRNA precursors in vivo. Rexo5 is ubiquitously expressed at low levels in somatic metazoan cells but extremely elevated in male and female germ cells. Loss of Rexo5 leads to increased nucleolar size, genomic instability, defective ribosome subunit export, and larval death. Loss of germline expression compromises gonadal growth and meiotic entry during germline development.
abstract_unstemmed	Non-coding RNA biogenesis in higher eukaryotes has not been fully characterized. Here, we studied the Drosophila melanogaster Rexo5 (CG8368) protein, a metazoan-specific member of the DEDDh 3′-5′ single-stranded RNA exonucleases, by genetic, biochemical, and RNA-sequencing approaches. Rexo5 is required for small nucleolar RNA (snoRNA) and rRNA biogenesis and is essential in D. melanogaster. Loss-of-function mutants accumulate improperly 3′ end-trimmed 28S rRNA, 5S rRNA, and snoRNA precursors in vivo. Rexo5 is ubiquitously expressed at low levels in somatic metazoan cells but extremely elevated in male and female germ cells. Loss of Rexo5 leads to increased nucleolar size, genomic instability, defective ribosome subunit export, and larval death. Loss of germline expression compromises gonadal growth and meiotic entry during germline development.
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container_issue	3
title_short	The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs
url	https://doi.org/10.1016/j.celrep.2017.09.067 https://doaj.org/article/06c6c57008cb4839b64703f881b49613 http://www.sciencedirect.com/science/article/pii/S2211124717313724 https://doaj.org/toc/2211-1247
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up_date	2024-07-03T13:20:08.206Z
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The Conserved RNA Exonuclease Rexo5 Is Required for 3′ End Maturation of 28S rRNA, 5S rRNA, and snoRNAs

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