Literature DB >> 77207

A new chromosome type replacing the double minutes in a mouse tumor.

A Levan, G Levan, N Mandahl.   

Abstract

For several years the SEWA mouse ascites tumor has been a carrier of double minute chromosomes (DMs), some 90% of its cells containing from one to several hundred DMs. In one specific subline of this tumor, the cells with DMs had decreased in frequency to less than 5% of the cells. At the same time, the stemline chromosome number had increased from 43 to around 50. This was due to the presence, in addition to the ordinary telocentric chromosomes, of a varying number of medium-sized metacentrics. The fact that these chromosomes deviated from ordinary mouse chromosomes in special features, such as median centromeric position, early DNA replication, and complete lack of centromeric heterochromatin, indicates that they represent a new type of chromosome. Their striking agreement with the DMs in many properties makes it tempting to associate their origin with the disappearance of the DMs.

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Year:  1978        PMID: 77207     DOI: 10.1159/000130836

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  14 in total

1.  Unstable and stable CAD gene amplification: importance of flanking sequences and nuclear environment in gene amplification.

Authors:  J Meinkoth; A M Killary; R E Fournier; G M Wahl
Journal:  Mol Cell Biol       Date:  1987-04       Impact factor: 4.272

2.  Analysis of the replication mode of double minutes using the PCC technique combined with BrdUrd labeling.

Authors:  S Takayama; Y Uwaike
Journal:  Chromosoma       Date:  1988-11       Impact factor: 4.316

3.  Increased dihydrofolate reductase, double minutes and increased nucleolar activation in methotrexate-resistant HeLa cells.

Authors:  J G Delinassios; M J Talieri
Journal:  Experientia       Date:  1983-12-15

4.  On the possibility of metabolic control of replicon "misfiring": relationship to emergence of malignant phenotypes in mammalian cell lineages.

Authors:  A Varshavsky
Journal:  Proc Natl Acad Sci U S A       Date:  1981-06       Impact factor: 11.205

5.  Marked increase in ribosomal RNA gene multiplicity in a rat hepatoma cell line.

Authors:  O J Miller; R Tantravahi; D A Miller; L C Yu; P Szabo; W Prensky
Journal:  Chromosoma       Date:  1979-02-21       Impact factor: 4.316

6.  MYCN gene amplification. Identification of cell populations containing double minutes and homogeneously staining regions in neuroblastoma tumors.

Authors:  M Yoshimoto; S R Caminada De Toledo; E M Monteiro Caran; M T de Seixas; M L de Martino Lee; S de Campos Vieira Abib; S M Vianna; S T Schettini; J Anderson Duffles Andrade
Journal:  Am J Pathol       Date:  1999-11       Impact factor: 4.307

Review 7.  Somatic cell fusion as a source of genetic rearrangement leading to metastatic variants.

Authors:  L Larizza; V Schirrmacher
Journal:  Cancer Metastasis Rev       Date:  1984       Impact factor: 9.264

8.  Gene amplification in a mouse embryo? Double minutes in cell lines independently derived from a Mus musculus X M. caroli fetus.

Authors:  J A Graves
Journal:  Chromosoma       Date:  1984       Impact factor: 4.316

9.  Amplified dihydrofolate reductase genes in unstably methotrexate-resistant cells are associated with double minute chromosomes.

Authors:  R J Kaufman; P C Brown; R T Schimke
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

10.  Regular pattern of karyotypic alterations accompanying gene amplification in Djungarian hamster cells: study of colchicine, adriablastin, and methotrexate resistance.

Authors:  B P Kopnin; J S Massino; A V Gudkov
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

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