Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen.

Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Oren, M. [verfasserIn] Bienz, B. [verfasserIn] Givol, D. [verfasserIn] Rechavi, G. [verfasserIn] Zakut, R. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	1983

Anmerkung:	© European Molecular Biology Organization 1983

Übergeordnetes Werk:	Enthalten in: The EMBO Journal - Nature Publishing Group UK, 2023, 2(1983), 10 vom: 01. Okt., Seite 1633-1639
Übergeordnetes Werk:	volume:2 ; year:1983 ; number:10 ; day:01 ; month:10 ; pages:1633-1639

Links:	Volltext

DOI / URN:	10.1002/j.1460-2075.1983.tb01637.x

Katalog-ID:	SPR057544751

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520			\|a Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation and immunoprecipitation with anti‐p53 monoclonal antibodies. The p53 mRNA appeared to be the only messenger species specifically selected by these clones. The size of the p53 mRNA was found to be approximately 2 kb, and its levels to vary substantially among different types of transformed cells. Evidence was found for the existence of two distinct p53‐specific genes in mouse genomic DNA. Two partially overlapping recombinant phage clones were obtained, both derived from the same p53‐specific genomic DNA region. The orientation of the various cDNA clones relative to that of the p53 mRNA was established by S1 analysis and the relationship between the cDNA clones and the genomic ones was determined by comparative restriction enzyme mapping and nucleic acid hybridization.
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allfields	10.1002/j.1460-2075.1983.tb01637.x doi (DE-627)SPR057544751 (SPR)j.1460-2075.1983.tb01637.x-e DE-627 ger DE-627 rakwb eng Oren, M. verfasserin aut Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen. 1983 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 1983 Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation and immunoprecipitation with anti‐p53 monoclonal antibodies. The p53 mRNA appeared to be the only messenger species specifically selected by these clones. The size of the p53 mRNA was found to be approximately 2 kb, and its levels to vary substantially among different types of transformed cells. Evidence was found for the existence of two distinct p53‐specific genes in mouse genomic DNA. Two partially overlapping recombinant phage clones were obtained, both derived from the same p53‐specific genomic DNA region. The orientation of the various cDNA clones relative to that of the p53 mRNA was established by S1 analysis and the relationship between the cDNA clones and the genomic ones was determined by comparative restriction enzyme mapping and nucleic acid hybridization. Bienz, B. verfasserin aut Givol, D. verfasserin aut Rechavi, G. verfasserin aut Zakut, R. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 2(1983), 10 vom: 01. Okt., Seite 1633-1639 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:2 year:1983 number:10 day:01 month:10 pages:1633-1639 https://dx.doi.org/10.1002/j.1460-2075.1983.tb01637.x X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 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_213 GBV_ILN_230 GBV_ILN_252 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2021 GBV_ILN_2050 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 1983 10 01 10 1633-1639
spelling	10.1002/j.1460-2075.1983.tb01637.x doi (DE-627)SPR057544751 (SPR)j.1460-2075.1983.tb01637.x-e DE-627 ger DE-627 rakwb eng Oren, M. verfasserin aut Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen. 1983 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 1983 Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation and immunoprecipitation with anti‐p53 monoclonal antibodies. The p53 mRNA appeared to be the only messenger species specifically selected by these clones. The size of the p53 mRNA was found to be approximately 2 kb, and its levels to vary substantially among different types of transformed cells. Evidence was found for the existence of two distinct p53‐specific genes in mouse genomic DNA. Two partially overlapping recombinant phage clones were obtained, both derived from the same p53‐specific genomic DNA region. The orientation of the various cDNA clones relative to that of the p53 mRNA was established by S1 analysis and the relationship between the cDNA clones and the genomic ones was determined by comparative restriction enzyme mapping and nucleic acid hybridization. Bienz, B. verfasserin aut Givol, D. verfasserin aut Rechavi, G. verfasserin aut Zakut, R. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 2(1983), 10 vom: 01. Okt., Seite 1633-1639 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:2 year:1983 number:10 day:01 month:10 pages:1633-1639 https://dx.doi.org/10.1002/j.1460-2075.1983.tb01637.x X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 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_213 GBV_ILN_230 GBV_ILN_252 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2021 GBV_ILN_2050 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 1983 10 01 10 1633-1639
allfields_unstemmed	10.1002/j.1460-2075.1983.tb01637.x doi (DE-627)SPR057544751 (SPR)j.1460-2075.1983.tb01637.x-e DE-627 ger DE-627 rakwb eng Oren, M. verfasserin aut Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen. 1983 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 1983 Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation and immunoprecipitation with anti‐p53 monoclonal antibodies. The p53 mRNA appeared to be the only messenger species specifically selected by these clones. The size of the p53 mRNA was found to be approximately 2 kb, and its levels to vary substantially among different types of transformed cells. Evidence was found for the existence of two distinct p53‐specific genes in mouse genomic DNA. Two partially overlapping recombinant phage clones were obtained, both derived from the same p53‐specific genomic DNA region. The orientation of the various cDNA clones relative to that of the p53 mRNA was established by S1 analysis and the relationship between the cDNA clones and the genomic ones was determined by comparative restriction enzyme mapping and nucleic acid hybridization. Bienz, B. verfasserin aut Givol, D. verfasserin aut Rechavi, G. verfasserin aut Zakut, R. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 2(1983), 10 vom: 01. Okt., Seite 1633-1639 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:2 year:1983 number:10 day:01 month:10 pages:1633-1639 https://dx.doi.org/10.1002/j.1460-2075.1983.tb01637.x X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 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_213 GBV_ILN_230 GBV_ILN_252 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2021 GBV_ILN_2050 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 1983 10 01 10 1633-1639
allfieldsGer	10.1002/j.1460-2075.1983.tb01637.x doi (DE-627)SPR057544751 (SPR)j.1460-2075.1983.tb01637.x-e DE-627 ger DE-627 rakwb eng Oren, M. verfasserin aut Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen. 1983 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 1983 Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation and immunoprecipitation with anti‐p53 monoclonal antibodies. The p53 mRNA appeared to be the only messenger species specifically selected by these clones. The size of the p53 mRNA was found to be approximately 2 kb, and its levels to vary substantially among different types of transformed cells. Evidence was found for the existence of two distinct p53‐specific genes in mouse genomic DNA. Two partially overlapping recombinant phage clones were obtained, both derived from the same p53‐specific genomic DNA region. The orientation of the various cDNA clones relative to that of the p53 mRNA was established by S1 analysis and the relationship between the cDNA clones and the genomic ones was determined by comparative restriction enzyme mapping and nucleic acid hybridization. Bienz, B. verfasserin aut Givol, D. verfasserin aut Rechavi, G. verfasserin aut Zakut, R. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 2(1983), 10 vom: 01. Okt., Seite 1633-1639 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:2 year:1983 number:10 day:01 month:10 pages:1633-1639 https://dx.doi.org/10.1002/j.1460-2075.1983.tb01637.x X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 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_213 GBV_ILN_230 GBV_ILN_252 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2021 GBV_ILN_2050 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 1983 10 01 10 1633-1639
allfieldsSound	10.1002/j.1460-2075.1983.tb01637.x doi (DE-627)SPR057544751 (SPR)j.1460-2075.1983.tb01637.x-e DE-627 ger DE-627 rakwb eng Oren, M. verfasserin aut Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen. 1983 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © European Molecular Biology Organization 1983 Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation and immunoprecipitation with anti‐p53 monoclonal antibodies. The p53 mRNA appeared to be the only messenger species specifically selected by these clones. The size of the p53 mRNA was found to be approximately 2 kb, and its levels to vary substantially among different types of transformed cells. Evidence was found for the existence of two distinct p53‐specific genes in mouse genomic DNA. Two partially overlapping recombinant phage clones were obtained, both derived from the same p53‐specific genomic DNA region. The orientation of the various cDNA clones relative to that of the p53 mRNA was established by S1 analysis and the relationship between the cDNA clones and the genomic ones was determined by comparative restriction enzyme mapping and nucleic acid hybridization. Bienz, B. verfasserin aut Givol, D. verfasserin aut Rechavi, G. verfasserin aut Zakut, R. verfasserin aut Enthalten in The EMBO Journal Nature Publishing Group UK, 2023 2(1983), 10 vom: 01. Okt., Seite 1633-1639 (DE-627)266022529 (DE-600)1467419-1 1460-2075 nnns volume:2 year:1983 number:10 day:01 month:10 pages:1633-1639 https://dx.doi.org/10.1002/j.1460-2075.1983.tb01637.x X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_72 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_213 GBV_ILN_230 GBV_ILN_252 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_2021 GBV_ILN_2050 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 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_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2 1983 10 01 10 1633-1639
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author	Oren, M.
spellingShingle	Oren, M. Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen.
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topic_title	Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen
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title	Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen.
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title_sort	analysis of recombinant dna clones specific for the murine p53 cellular tumor antigen
title_auth	Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen.
abstract	Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation and immunoprecipitation with anti‐p53 monoclonal antibodies. The p53 mRNA appeared to be the only messenger species specifically selected by these clones. The size of the p53 mRNA was found to be approximately 2 kb, and its levels to vary substantially among different types of transformed cells. Evidence was found for the existence of two distinct p53‐specific genes in mouse genomic DNA. Two partially overlapping recombinant phage clones were obtained, both derived from the same p53‐specific genomic DNA region. The orientation of the various cDNA clones relative to that of the p53 mRNA was established by S1 analysis and the relationship between the cDNA clones and the genomic ones was determined by comparative restriction enzyme mapping and nucleic acid hybridization. © European Molecular Biology Organization 1983
abstractGer	Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation and immunoprecipitation with anti‐p53 monoclonal antibodies. The p53 mRNA appeared to be the only messenger species specifically selected by these clones. The size of the p53 mRNA was found to be approximately 2 kb, and its levels to vary substantially among different types of transformed cells. Evidence was found for the existence of two distinct p53‐specific genes in mouse genomic DNA. Two partially overlapping recombinant phage clones were obtained, both derived from the same p53‐specific genomic DNA region. The orientation of the various cDNA clones relative to that of the p53 mRNA was established by S1 analysis and the relationship between the cDNA clones and the genomic ones was determined by comparative restriction enzyme mapping and nucleic acid hybridization. © European Molecular Biology Organization 1983
abstract_unstemmed	Abstract Three cDNA clones, corresponding to two non‐overlapping regions of the mRNA coding for the mouse p53 cellular tumor antigen, were isolated and characterized. In hybridization‐selection assays, these clones were capable of selectively binding p53 mRNA, as demonstrated by in vitro translation and immunoprecipitation with anti‐p53 monoclonal antibodies. The p53 mRNA appeared to be the only messenger species specifically selected by these clones. The size of the p53 mRNA was found to be approximately 2 kb, and its levels to vary substantially among different types of transformed cells. Evidence was found for the existence of two distinct p53‐specific genes in mouse genomic DNA. Two partially overlapping recombinant phage clones were obtained, both derived from the same p53‐specific genomic DNA region. The orientation of the various cDNA clones relative to that of the p53 mRNA was established by S1 analysis and the relationship between the cDNA clones and the genomic ones was determined by comparative restriction enzyme mapping and nucleic acid hybridization. © European Molecular Biology Organization 1983
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title_short	Analysis of recombinant DNA clones specific for the murine p53 cellular tumor antigen.
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