The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis
Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homol...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
He, Hongjiang [verfasserIn] Zhu, Dan [verfasserIn] Sun, Ji [verfasserIn] Pei, Rong [verfasserIn] Jia, Shenshan [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2011 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Molecular biology - Moscow : MAIK Nauka/Interperiodica Publ., 1997, 45(2011), 3 vom: 16. Juni |
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| Übergeordnetes Werk: |
volume:45 ; year:2011 ; number:3 ; day:16 ; month:06 |
| Links: |
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| DOI / URN: |
10.1134/S0026893311020099 |
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| Katalog-ID: |
SPR015585336 |
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| 100 | 1 | |a He, Hongjiang |e verfasserin |4 aut | |
| 245 | 1 | 4 | |a The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis |
| 264 | 1 | |c 2011 | |
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| 337 | |a Computermedien |b c |2 rdamedia | ||
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| 520 | |a Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homolog), a protein containing a WGG motif, which has no known specific function, although this protein is conserved during evolution across different species. The cDNA sequence contains a 576 bp open reading frame, encoding a 191 amino acid protein with a predicted molecular mass of 20.9 kDa. Northern blot analysis revealed broad TSR2 mRNA expression in human tissues. Overexpression of TSR2 in human epidermal HEp-2 cells inhibited the transcriptional activity of NF-κB, with or without tumor necrosis factor α stimulus, and induced HEp-2 cell apoptosis. This data for the first time suggests that TSR2 is involved in the NF-κB signaling pathway and may regulate apoptosis. | ||
| 650 | 4 | |a TSR2 |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a nuclear factor-kappaB |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a apoptosis |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a laryngeal cancer |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Zhu, Dan |e verfasserin |4 aut | |
| 700 | 1 | |a Sun, Ji |e verfasserin |4 aut | |
| 700 | 1 | |a Pei, Rong |e verfasserin |4 aut | |
| 700 | 1 | |a Jia, Shenshan |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Molecular biology |d Moscow : MAIK Nauka/Interperiodica Publ., 1997 |g 45(2011), 3 vom: 16. Juni |w (DE-627)324825382 |w (DE-600)2031117-5 |x 1608-3245 |7 nnns |
| 773 | 1 | 8 | |g volume:45 |g year:2011 |g number:3 |g day:16 |g month:06 |
| 856 | 4 | 0 | |u https://dx.doi.org/10.1134/S0026893311020099 |z lizenzpflichtig |3 Volltext |
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| 912 | |a GBV_ILN_22 | ||
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| 912 | |a GBV_ILN_31 | ||
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| 912 | |a GBV_ILN_39 | ||
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| 912 | |a GBV_ILN_60 | ||
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| 912 | |a GBV_ILN_63 | ||
| 912 | |a GBV_ILN_69 | ||
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| 912 | |a GBV_ILN_73 | ||
| 912 | |a GBV_ILN_74 | ||
| 912 | |a GBV_ILN_90 | ||
| 912 | |a GBV_ILN_95 | ||
| 912 | |a GBV_ILN_100 | ||
| 912 | |a GBV_ILN_101 | ||
| 912 | |a GBV_ILN_105 | ||
| 912 | |a GBV_ILN_110 | ||
| 912 | |a GBV_ILN_120 | ||
| 912 | |a GBV_ILN_138 | ||
| 912 | |a GBV_ILN_150 | ||
| 912 | |a GBV_ILN_151 | ||
| 912 | |a GBV_ILN_152 | ||
| 912 | |a GBV_ILN_161 | ||
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| 912 | |a GBV_ILN_171 | ||
| 912 | |a GBV_ILN_187 | ||
| 912 | |a GBV_ILN_213 | ||
| 912 | |a GBV_ILN_224 | ||
| 912 | |a GBV_ILN_230 | ||
| 912 | |a GBV_ILN_250 | ||
| 912 | |a GBV_ILN_281 | ||
| 912 | |a GBV_ILN_285 | ||
| 912 | |a GBV_ILN_293 | ||
| 912 | |a GBV_ILN_370 | ||
| 912 | |a GBV_ILN_602 | ||
| 912 | |a GBV_ILN_636 | ||
| 912 | |a GBV_ILN_702 | ||
| 912 | |a GBV_ILN_2001 | ||
| 912 | |a GBV_ILN_2003 | ||
| 912 | |a GBV_ILN_2004 | ||
| 912 | |a GBV_ILN_2005 | ||
| 912 | |a GBV_ILN_2006 | ||
| 912 | |a GBV_ILN_2007 | ||
| 912 | |a GBV_ILN_2008 | ||
| 912 | |a GBV_ILN_2009 | ||
| 912 | |a GBV_ILN_2010 | ||
| 912 | |a GBV_ILN_2011 | ||
| 912 | |a GBV_ILN_2014 | ||
| 912 | |a GBV_ILN_2015 | ||
| 912 | |a GBV_ILN_2020 | ||
| 912 | |a GBV_ILN_2021 | ||
| 912 | |a GBV_ILN_2025 | ||
| 912 | |a GBV_ILN_2026 | ||
| 912 | |a GBV_ILN_2027 | ||
| 912 | |a GBV_ILN_2031 | ||
| 912 | |a GBV_ILN_2034 | ||
| 912 | |a GBV_ILN_2037 | ||
| 912 | |a GBV_ILN_2038 | ||
| 912 | |a GBV_ILN_2039 | ||
| 912 | |a GBV_ILN_2044 | ||
| 912 | |a GBV_ILN_2048 | ||
| 912 | |a GBV_ILN_2049 | ||
| 912 | |a GBV_ILN_2050 | ||
| 912 | |a GBV_ILN_2055 | ||
| 912 | |a GBV_ILN_2057 | ||
| 912 | |a GBV_ILN_2059 | ||
| 912 | |a GBV_ILN_2061 | ||
| 912 | |a GBV_ILN_2064 | ||
| 912 | |a GBV_ILN_2065 | ||
| 912 | |a GBV_ILN_2068 | ||
| 912 | |a GBV_ILN_2070 | ||
| 912 | |a GBV_ILN_2086 | ||
| 912 | |a GBV_ILN_2088 | ||
| 912 | |a GBV_ILN_2093 | ||
| 912 | |a GBV_ILN_2106 | ||
| 912 | |a GBV_ILN_2107 | ||
| 912 | |a GBV_ILN_2108 | ||
| 912 | |a GBV_ILN_2110 | ||
| 912 | |a GBV_ILN_2111 | ||
| 912 | |a GBV_ILN_2112 | ||
| 912 | |a GBV_ILN_2113 | ||
| 912 | |a GBV_ILN_2116 | ||
| 912 | |a GBV_ILN_2118 | ||
| 912 | |a GBV_ILN_2119 | ||
| 912 | |a GBV_ILN_2122 | ||
| 912 | |a GBV_ILN_2129 | ||
| 912 | |a GBV_ILN_2143 | ||
| 912 | |a GBV_ILN_2144 | ||
| 912 | |a GBV_ILN_2147 | ||
| 912 | |a GBV_ILN_2148 | ||
| 912 | |a GBV_ILN_2152 | ||
| 912 | |a GBV_ILN_2153 | ||
| 912 | |a GBV_ILN_2188 | ||
| 912 | |a GBV_ILN_2190 | ||
| 912 | |a GBV_ILN_2232 | ||
| 912 | |a GBV_ILN_2336 | ||
| 912 | |a GBV_ILN_2446 | ||
| 912 | |a GBV_ILN_2470 | ||
| 912 | |a GBV_ILN_2472 | ||
| 912 | |a GBV_ILN_2507 | ||
| 912 | |a GBV_ILN_2522 | ||
| 912 | |a GBV_ILN_2548 | ||
| 912 | |a GBV_ILN_4012 | ||
| 912 | |a GBV_ILN_4035 | ||
| 912 | |a GBV_ILN_4037 | ||
| 912 | |a GBV_ILN_4046 | ||
| 912 | |a GBV_ILN_4112 | ||
| 912 | |a GBV_ILN_4125 | ||
| 912 | |a GBV_ILN_4126 | ||
| 912 | |a GBV_ILN_4242 | ||
| 912 | |a GBV_ILN_4246 | ||
| 912 | |a GBV_ILN_4249 | ||
| 912 | |a GBV_ILN_4251 | ||
| 912 | |a GBV_ILN_4305 | ||
| 912 | |a GBV_ILN_4306 | ||
| 912 | |a GBV_ILN_4307 | ||
| 912 | |a GBV_ILN_4313 | ||
| 912 | |a GBV_ILN_4322 | ||
| 912 | |a GBV_ILN_4323 | ||
| 912 | |a GBV_ILN_4324 | ||
| 912 | |a GBV_ILN_4325 | ||
| 912 | |a GBV_ILN_4326 | ||
| 912 | |a GBV_ILN_4333 | ||
| 912 | |a GBV_ILN_4334 | ||
| 912 | |a GBV_ILN_4335 | ||
| 912 | |a GBV_ILN_4336 | ||
| 912 | |a GBV_ILN_4338 | ||
| 912 | |a GBV_ILN_4393 | ||
| 912 | |a GBV_ILN_4700 | ||
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| allfields |
10.1134/S0026893311020099 doi (DE-627)SPR015585336 (SPR)S0026893311020099-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl He, Hongjiang verfasserin aut The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homolog), a protein containing a WGG motif, which has no known specific function, although this protein is conserved during evolution across different species. The cDNA sequence contains a 576 bp open reading frame, encoding a 191 amino acid protein with a predicted molecular mass of 20.9 kDa. Northern blot analysis revealed broad TSR2 mRNA expression in human tissues. Overexpression of TSR2 in human epidermal HEp-2 cells inhibited the transcriptional activity of NF-κB, with or without tumor necrosis factor α stimulus, and induced HEp-2 cell apoptosis. This data for the first time suggests that TSR2 is involved in the NF-κB signaling pathway and may regulate apoptosis. TSR2 (dpeaa)DE-He213 nuclear factor-kappaB (dpeaa)DE-He213 apoptosis (dpeaa)DE-He213 laryngeal cancer (dpeaa)DE-He213 Zhu, Dan verfasserin aut Sun, Ji verfasserin aut Pei, Rong verfasserin aut Jia, Shenshan verfasserin aut Enthalten in Molecular biology Moscow : MAIK Nauka/Interperiodica Publ., 1997 45(2011), 3 vom: 16. Juni (DE-627)324825382 (DE-600)2031117-5 1608-3245 nnns volume:45 year:2011 number:3 day:16 month:06 https://dx.doi.org/10.1134/S0026893311020099 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2011 3 16 06 |
| spelling |
10.1134/S0026893311020099 doi (DE-627)SPR015585336 (SPR)S0026893311020099-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl He, Hongjiang verfasserin aut The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homolog), a protein containing a WGG motif, which has no known specific function, although this protein is conserved during evolution across different species. The cDNA sequence contains a 576 bp open reading frame, encoding a 191 amino acid protein with a predicted molecular mass of 20.9 kDa. Northern blot analysis revealed broad TSR2 mRNA expression in human tissues. Overexpression of TSR2 in human epidermal HEp-2 cells inhibited the transcriptional activity of NF-κB, with or without tumor necrosis factor α stimulus, and induced HEp-2 cell apoptosis. This data for the first time suggests that TSR2 is involved in the NF-κB signaling pathway and may regulate apoptosis. TSR2 (dpeaa)DE-He213 nuclear factor-kappaB (dpeaa)DE-He213 apoptosis (dpeaa)DE-He213 laryngeal cancer (dpeaa)DE-He213 Zhu, Dan verfasserin aut Sun, Ji verfasserin aut Pei, Rong verfasserin aut Jia, Shenshan verfasserin aut Enthalten in Molecular biology Moscow : MAIK Nauka/Interperiodica Publ., 1997 45(2011), 3 vom: 16. Juni (DE-627)324825382 (DE-600)2031117-5 1608-3245 nnns volume:45 year:2011 number:3 day:16 month:06 https://dx.doi.org/10.1134/S0026893311020099 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2011 3 16 06 |
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10.1134/S0026893311020099 doi (DE-627)SPR015585336 (SPR)S0026893311020099-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl He, Hongjiang verfasserin aut The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homolog), a protein containing a WGG motif, which has no known specific function, although this protein is conserved during evolution across different species. The cDNA sequence contains a 576 bp open reading frame, encoding a 191 amino acid protein with a predicted molecular mass of 20.9 kDa. Northern blot analysis revealed broad TSR2 mRNA expression in human tissues. Overexpression of TSR2 in human epidermal HEp-2 cells inhibited the transcriptional activity of NF-κB, with or without tumor necrosis factor α stimulus, and induced HEp-2 cell apoptosis. This data for the first time suggests that TSR2 is involved in the NF-κB signaling pathway and may regulate apoptosis. TSR2 (dpeaa)DE-He213 nuclear factor-kappaB (dpeaa)DE-He213 apoptosis (dpeaa)DE-He213 laryngeal cancer (dpeaa)DE-He213 Zhu, Dan verfasserin aut Sun, Ji verfasserin aut Pei, Rong verfasserin aut Jia, Shenshan verfasserin aut Enthalten in Molecular biology Moscow : MAIK Nauka/Interperiodica Publ., 1997 45(2011), 3 vom: 16. Juni (DE-627)324825382 (DE-600)2031117-5 1608-3245 nnns volume:45 year:2011 number:3 day:16 month:06 https://dx.doi.org/10.1134/S0026893311020099 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2011 3 16 06 |
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10.1134/S0026893311020099 doi (DE-627)SPR015585336 (SPR)S0026893311020099-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl He, Hongjiang verfasserin aut The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homolog), a protein containing a WGG motif, which has no known specific function, although this protein is conserved during evolution across different species. The cDNA sequence contains a 576 bp open reading frame, encoding a 191 amino acid protein with a predicted molecular mass of 20.9 kDa. Northern blot analysis revealed broad TSR2 mRNA expression in human tissues. Overexpression of TSR2 in human epidermal HEp-2 cells inhibited the transcriptional activity of NF-κB, with or without tumor necrosis factor α stimulus, and induced HEp-2 cell apoptosis. This data for the first time suggests that TSR2 is involved in the NF-κB signaling pathway and may regulate apoptosis. TSR2 (dpeaa)DE-He213 nuclear factor-kappaB (dpeaa)DE-He213 apoptosis (dpeaa)DE-He213 laryngeal cancer (dpeaa)DE-He213 Zhu, Dan verfasserin aut Sun, Ji verfasserin aut Pei, Rong verfasserin aut Jia, Shenshan verfasserin aut Enthalten in Molecular biology Moscow : MAIK Nauka/Interperiodica Publ., 1997 45(2011), 3 vom: 16. Juni (DE-627)324825382 (DE-600)2031117-5 1608-3245 nnns volume:45 year:2011 number:3 day:16 month:06 https://dx.doi.org/10.1134/S0026893311020099 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2011 3 16 06 |
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10.1134/S0026893311020099 doi (DE-627)SPR015585336 (SPR)S0026893311020099-e DE-627 ger DE-627 rakwb eng 570 ASE 42.00 bkl He, Hongjiang verfasserin aut The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homolog), a protein containing a WGG motif, which has no known specific function, although this protein is conserved during evolution across different species. The cDNA sequence contains a 576 bp open reading frame, encoding a 191 amino acid protein with a predicted molecular mass of 20.9 kDa. Northern blot analysis revealed broad TSR2 mRNA expression in human tissues. Overexpression of TSR2 in human epidermal HEp-2 cells inhibited the transcriptional activity of NF-κB, with or without tumor necrosis factor α stimulus, and induced HEp-2 cell apoptosis. This data for the first time suggests that TSR2 is involved in the NF-κB signaling pathway and may regulate apoptosis. TSR2 (dpeaa)DE-He213 nuclear factor-kappaB (dpeaa)DE-He213 apoptosis (dpeaa)DE-He213 laryngeal cancer (dpeaa)DE-He213 Zhu, Dan verfasserin aut Sun, Ji verfasserin aut Pei, Rong verfasserin aut Jia, Shenshan verfasserin aut Enthalten in Molecular biology Moscow : MAIK Nauka/Interperiodica Publ., 1997 45(2011), 3 vom: 16. Juni (DE-627)324825382 (DE-600)2031117-5 1608-3245 nnns volume:45 year:2011 number:3 day:16 month:06 https://dx.doi.org/10.1134/S0026893311020099 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 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_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 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_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 45 2011 3 16 06 |
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He, Hongjiang @@aut@@ Zhu, Dan @@aut@@ Sun, Ji @@aut@@ Pei, Rong @@aut@@ Jia, Shenshan @@aut@@ |
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| author |
He, Hongjiang |
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He, Hongjiang ddc 570 bkl 42.00 misc TSR2 misc nuclear factor-kappaB misc apoptosis misc laryngeal cancer The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis |
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570 ASE 42.00 bkl The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis TSR2 (dpeaa)DE-He213 nuclear factor-kappaB (dpeaa)DE-He213 apoptosis (dpeaa)DE-He213 laryngeal cancer (dpeaa)DE-He213 |
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ddc 570 bkl 42.00 misc TSR2 misc nuclear factor-kappaB misc apoptosis misc laryngeal cancer |
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The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis |
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The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis |
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novel protein tsr2 inhibits the transcriptional activity of nuclear factor-κb and induces apoptosis |
| title_auth |
The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis |
| abstract |
Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homolog), a protein containing a WGG motif, which has no known specific function, although this protein is conserved during evolution across different species. The cDNA sequence contains a 576 bp open reading frame, encoding a 191 amino acid protein with a predicted molecular mass of 20.9 kDa. Northern blot analysis revealed broad TSR2 mRNA expression in human tissues. Overexpression of TSR2 in human epidermal HEp-2 cells inhibited the transcriptional activity of NF-κB, with or without tumor necrosis factor α stimulus, and induced HEp-2 cell apoptosis. This data for the first time suggests that TSR2 is involved in the NF-κB signaling pathway and may regulate apoptosis. |
| abstractGer |
Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homolog), a protein containing a WGG motif, which has no known specific function, although this protein is conserved during evolution across different species. The cDNA sequence contains a 576 bp open reading frame, encoding a 191 amino acid protein with a predicted molecular mass of 20.9 kDa. Northern blot analysis revealed broad TSR2 mRNA expression in human tissues. Overexpression of TSR2 in human epidermal HEp-2 cells inhibited the transcriptional activity of NF-κB, with or without tumor necrosis factor α stimulus, and induced HEp-2 cell apoptosis. This data for the first time suggests that TSR2 is involved in the NF-κB signaling pathway and may regulate apoptosis. |
| abstract_unstemmed |
Abstract The nuclear factor-κB (NF-κB) pathway is involved in a variety of cellular functions, including cell proliferation, differentiation, development, oncogenesis, and apoptosis. In this study, we report on cloning and characterization of the human TSR2 (also known as 20S rRNA accumulation homolog), a protein containing a WGG motif, which has no known specific function, although this protein is conserved during evolution across different species. The cDNA sequence contains a 576 bp open reading frame, encoding a 191 amino acid protein with a predicted molecular mass of 20.9 kDa. Northern blot analysis revealed broad TSR2 mRNA expression in human tissues. Overexpression of TSR2 in human epidermal HEp-2 cells inhibited the transcriptional activity of NF-κB, with or without tumor necrosis factor α stimulus, and induced HEp-2 cell apoptosis. This data for the first time suggests that TSR2 is involved in the NF-κB signaling pathway and may regulate apoptosis. |
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| title_short |
The Novel protein TSR2 inhibits the transcriptional activity of nuclear factor-κB and induces apoptosis |
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https://dx.doi.org/10.1134/S0026893311020099 |
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| author2 |
Zhu, Dan Sun, Ji Pei, Rong Jia, Shenshan |
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Zhu, Dan Sun, Ji Pei, Rong Jia, Shenshan |
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| doi_str |
10.1134/S0026893311020099 |
| up_date |
2024-07-03T17:10:51.875Z |
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| score |
7.400818 |