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Frequency and Types of Point Mutation at the 12th Codon of the c‐Ki‐ras Gene Found in Pancreatic Cancers from Japanese Patients

Point mutations at the 12th codon of c‐Ki‐ras in pancreatic cancer from Japanese patients were examined using the polymerase chain reaction, followed by cloning of the amplified gene fragments in pTZ phagemid and nucleotide sequence determination. The frequency of the point mutations found in the tu...

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Autores principales: Mariyama, Mariko, Kishi, Kiyozo, Nakamura, Kozo, Obata, Hiroshi, Nishimura, Susumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917815/
https://www.ncbi.nlm.nih.gov/pubmed/2507485
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01687.x
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author Mariyama, Mariko
Kishi, Kiyozo
Nakamura, Kozo
Obata, Hiroshi
Nishimura, Susumu
author_facet Mariyama, Mariko
Kishi, Kiyozo
Nakamura, Kozo
Obata, Hiroshi
Nishimura, Susumu
author_sort Mariyama, Mariko
collection PubMed
description Point mutations at the 12th codon of c‐Ki‐ras in pancreatic cancer from Japanese patients were examined using the polymerase chain reaction, followed by cloning of the amplified gene fragments in pTZ phagemid and nucleotide sequence determination. The frequency of the point mutations found in the tumors was quite high (75%). The mutation most frequently detected was a G→A transition at the second position of codon 12 (GGT→GAT), but other types of mutations such as GGT→GTT and GGT→CGT were also found. In one case, silent mutation of GGT to GGC was detected in addition to the frequent mutation of GGT to GAT, These observations suggest that the 12th codon of pancreatic c‐Ki‐ras is highly mutatable.
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spelling pubmed-59178152018-05-11 Frequency and Types of Point Mutation at the 12th Codon of the c‐Ki‐ras Gene Found in Pancreatic Cancers from Japanese Patients Mariyama, Mariko Kishi, Kiyozo Nakamura, Kozo Obata, Hiroshi Nishimura, Susumu Jpn J Cancer Res Rapid Communication Point mutations at the 12th codon of c‐Ki‐ras in pancreatic cancer from Japanese patients were examined using the polymerase chain reaction, followed by cloning of the amplified gene fragments in pTZ phagemid and nucleotide sequence determination. The frequency of the point mutations found in the tumors was quite high (75%). The mutation most frequently detected was a G→A transition at the second position of codon 12 (GGT→GAT), but other types of mutations such as GGT→GTT and GGT→CGT were also found. In one case, silent mutation of GGT to GGC was detected in addition to the frequent mutation of GGT to GAT, These observations suggest that the 12th codon of pancreatic c‐Ki‐ras is highly mutatable. Blackwell Publishing Ltd 1989-07 /pmc/articles/PMC5917815/ /pubmed/2507485 http://dx.doi.org/10.1111/j.1349-7006.1989.tb01687.x Text en
spellingShingle Rapid Communication
Mariyama, Mariko
Kishi, Kiyozo
Nakamura, Kozo
Obata, Hiroshi
Nishimura, Susumu
Frequency and Types of Point Mutation at the 12th Codon of the c‐Ki‐ras Gene Found in Pancreatic Cancers from Japanese Patients
title Frequency and Types of Point Mutation at the 12th Codon of the c‐Ki‐ras Gene Found in Pancreatic Cancers from Japanese Patients
title_full Frequency and Types of Point Mutation at the 12th Codon of the c‐Ki‐ras Gene Found in Pancreatic Cancers from Japanese Patients
title_fullStr Frequency and Types of Point Mutation at the 12th Codon of the c‐Ki‐ras Gene Found in Pancreatic Cancers from Japanese Patients
title_full_unstemmed Frequency and Types of Point Mutation at the 12th Codon of the c‐Ki‐ras Gene Found in Pancreatic Cancers from Japanese Patients
title_short Frequency and Types of Point Mutation at the 12th Codon of the c‐Ki‐ras Gene Found in Pancreatic Cancers from Japanese Patients
title_sort frequency and types of point mutation at the 12th codon of the c‐ki‐ras gene found in pancreatic cancers from japanese patients
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917815/
https://www.ncbi.nlm.nih.gov/pubmed/2507485
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01687.x
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