Literature DB >> 6617768

Two distinct types of mitochondrial DNA segregation in mouse-rat hybrid cells. Stochastic segregation and chromosome-dependent segregation.

J Hayashi, Y Tagashira, M C Yoshida, K Ajiro, T Sekiguchi.   

Abstract

Two distinct patterns of mitochondrial DNA (mtDNA) segregation were found in different mouse-rat hybrid cell lines. On mouse-rat hybrid cell line, H2, retained complete sets of chromosomes and mtDNAs of both mouse and rat. Even after cultivation for about one year after cloning, the H2 cell population still retained both parental mtDNAs. However, when mtDNAs of H2 subclones were examined, it was found that some individual cells in the H2 cell population contained only mouse or only rat mtDNA, although they still retained complete sets of both kinds of parental chromosomes. This type of mtDNA segregation, named stochastic segregation, is bidirectional and may be caused by the repetition of random sharing of mouse and rat mtDNAs with daughter cells. This segregation occurred spontaneously during long-term cultivation. The second type of mtDNA segregation, named chromosome-dependent segregation, was found in the other mouse-rat hybrid cell lines that segregated either mouse or rat chromosomes. In these hybrid cells, chromosomes and mtDNA of the same species co-segregated. This second type of segregation is unidirectional. The types of mtDNA segregation appear to depend on the stability of the parental chromosomes in the hybrid cells. When both mouse and rat chromosomes retain stably, mtDNA shows stochastic segregation. On the contrary, when either species of chromosomes is segregated from the cells, mtDNA shows chromosome-dependent segregation.

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Year:  1983        PMID: 6617768     DOI: 10.1016/0014-4827(83)90270-7

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  12 in total

1.  Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues.

Authors:  Ekaterina Nekhaeva; Natalya D Bodyak; Yevgenya Kraytsberg; Sean B McGrath; Nathalie J Van Orsouw; Anna Pluzhnikov; Jeanne Y Wei; Jan Vijg; Konstantin Khrapko
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-09       Impact factor: 11.205

2.  Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybrids.

Authors:  L Kenyon; C T Moraes
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

3.  Maternal inheritance of mouse mtDNA in interspecific hybrids: segregation of the leaked paternal mtDNA followed by the prevention of subsequent paternal leakage.

Authors:  H Shitara; J I Hayashi; S Takahama; H Kaneda; H Yonekawa
Journal:  Genetics       Date:  1998-02       Impact factor: 4.562

4.  Is paternal mitochondrial DNA transferred to the offspring following intracytoplasmic sperm injection?

Authors:  M Houshmand; E Holme; C Hanson; U B Wennerholm; L Hamberger
Journal:  J Assist Reprod Genet       Date:  1997-04       Impact factor: 3.412

5.  Mitochondrial encephalomyopathies and cytochrome c oxidase deficiency: muscle culture study.

Authors:  I Nonaka; Y Koga; A Kikuchi; Y Goto
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

6.  Complete repopulation of mouse mitochondrial DNA-less cells with rat mitochondrial DNA restores mitochondrial translation but not mitochondrial respiratory function.

Authors:  M Yamaoka; K Isobe; H Shitara; H Yonekawa; S Miyabayashi; J I Hayashi
Journal:  Genetics       Date:  2000-05       Impact factor: 4.562

7.  Restoration of Mitochondrial Gene Expression Using a Cloned Human Gene in Chinese Hamster Lung Cell Mutant.

Authors:  Zaki A Sherif; Carolyn W Broome
Journal:  Adv Tech Biol Med       Date:  2015

8.  Mosaicism of mitochondria in mitochondrial myopathy: an electronmicroscopic analysis of cytochrome c oxidase.

Authors:  K Haginoya; S Miyabayashi; K Iinuma; K Tada
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

9.  Segregation of mitochondrial DNA in human somatic cell hybrids.

Authors:  F A White; C L Bunn
Journal:  Mol Gen Genet       Date:  1984

10.  Transmitochondrial mice as models for primary prevention of diseases caused by mutation in the tRNA(Lys) gene.

Authors:  Akinori Shimizu; Takayuki Mito; Chisato Hayashi; Emi Ogasawara; Ryusuke Koba; Issei Negishi; Keizo Takenaga; Kazuto Nakada; Jun-Ichi Hayashi
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-07       Impact factor: 11.205

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