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Normal Human Chromosome 1 Carries Suppressor Activity for Various Phenotypes of a Kirsten Murine Sarcoma Virus‐transformed NIH/3T3 Cell Line

In order to identify chromosomes that carry putative tumor‐suppressor genes for the various phenotypes of Kirsten sarcoma virus‐transformed NIH/3T3 (DT) cells, we performed microcell‐mediated chromosome transfer into DT cells. We first isolated mouse A9 clones, containing a single human chromosome 1...

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Detalles Bibliográficos
Autores principales: Yamada, Hideto, Horikawa, Izumi, Hashiba, Hiroki, Oshimura, Mitsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917993/
https://www.ncbi.nlm.nih.gov/pubmed/1702413
http://dx.doi.org/10.1111/j.1349-7006.1990.tb02519.x
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author Yamada, Hideto
Horikawa, Izumi
Hashiba, Hiroki
Oshimura, Mitsuo
author_facet Yamada, Hideto
Horikawa, Izumi
Hashiba, Hiroki
Oshimura, Mitsuo
author_sort Yamada, Hideto
collection PubMed
description In order to identify chromosomes that carry putative tumor‐suppressor genes for the various phenotypes of Kirsten sarcoma virus‐transformed NIH/3T3 (DT) cells, we performed microcell‐mediated chromosome transfer into DT cells. We first isolated mouse A9 clones, containing a single human chromosome 1, 11 or 12 tagged with pSV2‐neo plasmid DNA. Then, chromosome 1, 11 or 12 was transferred from the A9 clones into DT cells by microcell fusion. The growth rate, colony‐forming ability in soft agar and tumorigenicity of the DT cells were controlled by chromosome 1, but not by chromosome 11 or 12, indicating that normal human chromosome 1 carries a putative tumor‐suppressor gene(s) that affects various transformed phenotypes of DT cells.
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spelling pubmed-59179932018-05-11 Normal Human Chromosome 1 Carries Suppressor Activity for Various Phenotypes of a Kirsten Murine Sarcoma Virus‐transformed NIH/3T3 Cell Line Yamada, Hideto Horikawa, Izumi Hashiba, Hiroki Oshimura, Mitsuo Jpn J Cancer Res Rapid Communication In order to identify chromosomes that carry putative tumor‐suppressor genes for the various phenotypes of Kirsten sarcoma virus‐transformed NIH/3T3 (DT) cells, we performed microcell‐mediated chromosome transfer into DT cells. We first isolated mouse A9 clones, containing a single human chromosome 1, 11 or 12 tagged with pSV2‐neo plasmid DNA. Then, chromosome 1, 11 or 12 was transferred from the A9 clones into DT cells by microcell fusion. The growth rate, colony‐forming ability in soft agar and tumorigenicity of the DT cells were controlled by chromosome 1, but not by chromosome 11 or 12, indicating that normal human chromosome 1 carries a putative tumor‐suppressor gene(s) that affects various transformed phenotypes of DT cells. Blackwell Publishing Ltd 1990-11 /pmc/articles/PMC5917993/ /pubmed/1702413 http://dx.doi.org/10.1111/j.1349-7006.1990.tb02519.x Text en
spellingShingle Rapid Communication
Yamada, Hideto
Horikawa, Izumi
Hashiba, Hiroki
Oshimura, Mitsuo
Normal Human Chromosome 1 Carries Suppressor Activity for Various Phenotypes of a Kirsten Murine Sarcoma Virus‐transformed NIH/3T3 Cell Line
title Normal Human Chromosome 1 Carries Suppressor Activity for Various Phenotypes of a Kirsten Murine Sarcoma Virus‐transformed NIH/3T3 Cell Line
title_full Normal Human Chromosome 1 Carries Suppressor Activity for Various Phenotypes of a Kirsten Murine Sarcoma Virus‐transformed NIH/3T3 Cell Line
title_fullStr Normal Human Chromosome 1 Carries Suppressor Activity for Various Phenotypes of a Kirsten Murine Sarcoma Virus‐transformed NIH/3T3 Cell Line
title_full_unstemmed Normal Human Chromosome 1 Carries Suppressor Activity for Various Phenotypes of a Kirsten Murine Sarcoma Virus‐transformed NIH/3T3 Cell Line
title_short Normal Human Chromosome 1 Carries Suppressor Activity for Various Phenotypes of a Kirsten Murine Sarcoma Virus‐transformed NIH/3T3 Cell Line
title_sort normal human chromosome 1 carries suppressor activity for various phenotypes of a kirsten murine sarcoma virus‐transformed nih/3t3 cell line
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917993/
https://www.ncbi.nlm.nih.gov/pubmed/1702413
http://dx.doi.org/10.1111/j.1349-7006.1990.tb02519.x
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