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Transformation of NIH3T3 Cells with Synthetic c‐Ha‐ras Genes

Synthetic human c‐Ha‐ras genes in which amino acid codons were altered to those which are frequently used in highly expressed Escherichia coli genes were ligated to the 3′‐end of Rous sarcoma virus long terminal repeat. When NIH3T3 cells were transfected with the plasmids having those genes with val...

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Detalles Bibliográficos
Autores principales: Kamiya, Hiroyuki, Miura, Kazunobu, Ohtomo, Noriko, Koda, Toshiaki, Kakinuma, Mitsuaki, Nishimura, Susumu, Ohtsuka, Eiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917723/
https://www.ncbi.nlm.nih.gov/pubmed/2542206
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02291.x
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author Kamiya, Hiroyuki
Miura, Kazunobu
Ohtomo, Noriko
Koda, Toshiaki
Kakinuma, Mitsuaki
Nishimura, Susumu
Ohtsuka, Eiko
author_facet Kamiya, Hiroyuki
Miura, Kazunobu
Ohtomo, Noriko
Koda, Toshiaki
Kakinuma, Mitsuaki
Nishimura, Susumu
Ohtsuka, Eiko
author_sort Kamiya, Hiroyuki
collection PubMed
description Synthetic human c‐Ha‐ras genes in which amino acid codons were altered to those which are frequently used in highly expressed Escherichia coli genes were ligated to the 3′‐end of Rous sarcoma virus long terminal repeat. When NIH3T3 cells were transfected with the plasmids having those genes with valine at codon 12, leucine at codon 61 or arginine at codon 61, transformants were efficiently produced. These results indicated that the synthetic c‐Ha‐ras genes are expressed in a mammalian system even though their codon usage is altered to correspond with that of E. colt. This expression vector system should he useful for studies on the structure‐function relationships of c‐Ha‐ras, since the synthetic gene can be easily modified to have multiple base alterations, and can also be used simultaneously for the production of large amounts of p21 in E. coli for biochemical and biophysical studies.
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spelling pubmed-59177232018-05-11 Transformation of NIH3T3 Cells with Synthetic c‐Ha‐ras Genes Kamiya, Hiroyuki Miura, Kazunobu Ohtomo, Noriko Koda, Toshiaki Kakinuma, Mitsuaki Nishimura, Susumu Ohtsuka, Eiko Jpn J Cancer Res Rapid Communication Synthetic human c‐Ha‐ras genes in which amino acid codons were altered to those which are frequently used in highly expressed Escherichia coli genes were ligated to the 3′‐end of Rous sarcoma virus long terminal repeat. When NIH3T3 cells were transfected with the plasmids having those genes with valine at codon 12, leucine at codon 61 or arginine at codon 61, transformants were efficiently produced. These results indicated that the synthetic c‐Ha‐ras genes are expressed in a mammalian system even though their codon usage is altered to correspond with that of E. colt. This expression vector system should he useful for studies on the structure‐function relationships of c‐Ha‐ras, since the synthetic gene can be easily modified to have multiple base alterations, and can also be used simultaneously for the production of large amounts of p21 in E. coli for biochemical and biophysical studies. Blackwell Publishing Ltd 1989-03 /pmc/articles/PMC5917723/ /pubmed/2542206 http://dx.doi.org/10.1111/j.1349-7006.1989.tb02291.x Text en
spellingShingle Rapid Communication
Kamiya, Hiroyuki
Miura, Kazunobu
Ohtomo, Noriko
Koda, Toshiaki
Kakinuma, Mitsuaki
Nishimura, Susumu
Ohtsuka, Eiko
Transformation of NIH3T3 Cells with Synthetic c‐Ha‐ras Genes
title Transformation of NIH3T3 Cells with Synthetic c‐Ha‐ras Genes
title_full Transformation of NIH3T3 Cells with Synthetic c‐Ha‐ras Genes
title_fullStr Transformation of NIH3T3 Cells with Synthetic c‐Ha‐ras Genes
title_full_unstemmed Transformation of NIH3T3 Cells with Synthetic c‐Ha‐ras Genes
title_short Transformation of NIH3T3 Cells with Synthetic c‐Ha‐ras Genes
title_sort transformation of nih3t3 cells with synthetic c‐ha‐ras genes
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917723/
https://www.ncbi.nlm.nih.gov/pubmed/2542206
http://dx.doi.org/10.1111/j.1349-7006.1989.tb02291.x
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