Literature DB >> 7691058

Molecular biology of double-minute chromosomes.

P J Hahn1.   

Abstract

Double-minute chromosomes play a critical role in tumor cell genetics where they are frequently associated with the overexpression of oncogene products. They have been observed for many years in light microscopic examinations of metaphase chromosomes from tumor cells, but their origin remains unknown and is the subject of considerable speculation. However, molecular details of their structure and organization can now be described in conjunction with the microscopic examinations, to allow an evaluation of the various models that have been developed to explain the genesis of double-minutes. The evidence now favors simple models that invoke chromosome breakage and circularization of very large acentric chromosome fragments, permitting unequal segregation of the genes on the fragment during cell division. If there is selection for overexpression of one of the genes on the fragment, daughter cells with more fragments will grow faster than daughter cells with fewer fragments, and over time the population of cells will come to contain many double-minutes per cell.

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Year:  1993        PMID: 7691058     DOI: 10.1002/bies.950150707

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  36 in total

1.  Inverted repeats as genetic elements for promoting DNA inverted duplication: implications in gene amplification.

Authors:  C T Lin; W H Lin; Y L Lyu; J Whang-Peng
Journal:  Nucleic Acids Res       Date:  2001-09-01       Impact factor: 16.971

2.  Chromosomal and extrachromosomal instability of the cyclin D2 gene is induced by Myc overexpression.

Authors:  S Mai; J Hanley-Hyde; G J Rainey; T I Kuschak; J T Paul; T D Littlewood; H Mischak; L M Stevens; D W Henderson; J F Mushinski
Journal:  Neoplasia       Date:  1999-08       Impact factor: 5.715

3.  A cruciform-dumbbell model for inverted dimer formation mediated by inverted repeats.

Authors:  C T Lin; Y L Lyu; L F Liu
Journal:  Nucleic Acids Res       Date:  1997-08-01       Impact factor: 16.971

4.  Molecular structure of double-minute chromosomes bearing amplified copies of the epidermal growth factor receptor gene in gliomas.

Authors:  Nicolas Vogt; Sandrine-Hélène Lefèvre; Françoise Apiou; Anne-Marie Dutrillaux; Andrej Cör; Pascal Leuraud; Marie-France Poupon; Bernard Dutrillaux; Michelle Debatisse; Bernard Malfoy
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-21       Impact factor: 11.205

5.  A novel gene amplification system in yeast based on double rolling-circle replication.

Authors:  Takaaki Watanabe; Takashi Horiuchi
Journal:  EMBO J       Date:  2004-12-16       Impact factor: 11.598

6.  Gene amplification in a p53-deficient cell line requires cell cycle progression under conditions that generate DNA breakage.

Authors:  T G Paulson; A Almasan; L L Brody; G M Wahl
Journal:  Mol Cell Biol       Date:  1998-05       Impact factor: 4.272

7.  Cytogenetic analyses of a murine carcinoma cell line and six metastatic derivatives with different degrees of radioresistability.

Authors:  R J Jamasbi; M Q Ye; T M Norvell
Journal:  In Vitro Cell Dev Biol Anim       Date:  1997-02       Impact factor: 2.416

8.  DNA amplification by breakage/fusion/bridge cycles initiated by spontaneous telomere loss in a human cancer cell line.

Authors:  Anthony W I Lo; Laure Sabatier; Bijan Fouladi; Géraldine Pottier; Michelle Ricoul; John P Murnane
Journal:  Neoplasia       Date:  2002 Nov-Dec       Impact factor: 5.715

Review 9.  Mechanisms and consequences of aneuploidy and chromosome instability in the aging brain.

Authors:  Grasiella A Andriani; Jan Vijg; Cristina Montagna
Journal:  Mech Ageing Dev       Date:  2016-03-21       Impact factor: 5.432

Review 10.  DNA amplification: new insights into its mechanism.

Authors:  E Wintersberger
Journal:  Chromosoma       Date:  1994-04       Impact factor: 4.316

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