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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1989
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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. |
format | Online Article Text |
id | pubmed-5917723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
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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