Literature DB >> 3731049

Sequence of centromere separation: a mechanism for orderly separation of dicentrics.

B K Vig, R P Zinkowski.   

Abstract

Stable dicentric chromosomes from three mouse cell lines (viz., SEWA Rec4, brain tumor, and L-cells), as well as a human t(9;11) line were analyzed for the sequence in which the two centromeres separate. At prometaphase, as well as in many cells at midmetaphase, the dicentrics express the two centromeres in the form of two primary constrictions. As the cell advances to late metaphase, one of the constrictions loosens the two chromatids so that eventually there is no connection between them. The other centromere stays intact during this period and separates into two units at the metaanaphase junction along with the rest of the genome. The centromere that separates prematurely (out-of-phase) usually is the same in a given dicentric. It is proposed that such a prematurely separating centromere does not function as active element during chromatid migration. Apparently, in dicentrics some sort of control is exerted to eliminate the functioning of one centromere. The nature of such control is not understood at this time. The mouse dicentrics "synthesize" only one kinetochore as definable by antikinetochore antibody studies.

Entities:  

Mesh:

Year:  1986        PMID: 3731049     DOI: 10.1016/0165-4608(86)90027-0

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  11 in total

1.  Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorder.

Authors:  H Rivera; O Zuffardi; P Maraschio; A Caiulo; C Anichini; R Scarinci; R Vivarelli
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

2.  Sequence of centromere separation: separation in a quasi-stable mouse-human somatic cell hybrid.

Authors:  B K Vig; R S Athwal
Journal:  Chromosoma       Date:  1989-09       Impact factor: 4.316

3.  Detection of distinct structural domains within the primary constriction using autoantibodies.

Authors:  J B Rattner; B G Kingwell; M J Fritzler
Journal:  Chromosoma       Date:  1988       Impact factor: 4.316

4.  Sequence of centromere separation: characterization of multicentric chromosomes in a rat cell line.

Authors:  D Broccoli; N Paweletz; B K Vig
Journal:  Chromosoma       Date:  1989-06       Impact factor: 4.316

5.  Sequence of centromere separation: differential replication of pericentric heterochromatin in multicentric chromosomes.

Authors:  B K Vig; D Broccoli
Journal:  Chromosoma       Date:  1988       Impact factor: 4.316

6.  Sequence of centromere separation: generation of unstable multicentric chromosomes in a rat cell line.

Authors:  B K Vig; N Paweletz
Journal:  Chromosoma       Date:  1988       Impact factor: 4.316

7.  Heterochromatin associated with active versus inactive centromeres of mouse replicates at different times.

Authors:  B K Vig
Journal:  Experientia       Date:  1988-01-15

8.  Significance of structural chromosome aberrations in human sperm: analysis of induced aberrations.

Authors:  A Genescà; J Benet; M R Caballín; R Miró; J R Germà; J Egozcue
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

9.  Restriction endonuclease/nick translation procedure on fixed chromosomes of the Atlantic salmon fish cell line.

Authors:  M Abuín; P Martínez; L Sánchez
Journal:  Chromosome Res       Date:  1995-09       Impact factor: 5.239

10.  Novel cytogenetic expression of gene amplification in actinomycin D-resistant somatic cell hybrids: transfer of resistance by centric chromatin bodies.

Authors:  A H Jakobsson; U Arnason; A Levan; T Martinsson; C Hanson; G Levan
Journal:  Chromosoma       Date:  1987       Impact factor: 4.316

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.