Literature DB >> 9933410

The cenpB gene is not essential in mice.

M Kapoor1, R Montes de Oca Luna, G Liu, G Lozano, C Cummings, M Mancini, I Ouspenski, B R Brinkley, G S May.   

Abstract

Centromere protein B (CENP-B) is a centromeric DNA-binding protein that binds to alpha-satellite DNA at the 17 bp CENP-B box sequence. The binding of CENP-B, along with other proteins, to alpha-satellite DNA sequences at the centromere, is thought to package the DNA into heterochromatin subjacent to the kinetochore of mitotic chromosomes. To determine the importance of CENP-B to kinetochore assembly and function, we generated a mouse null for the cenpB gene. The deletion removed part of the promoter and the entire coding sequence except for the carboxyl-terminal 35 amino acids of the CENP-B polypeptide. Mice heterozygous or homozygous for the cenpB null mutation are viable and healthy, with no apparent defect in growth and morphology. We have established mouse embryo fibroblasts from heterozygous and homozygous cenpB null littermates. Microscopic analysis, using immunofluorescence and electron microscopy of the cultured cells, indicated that the centromere-kinetochore complex was intact and identical to control cells. Mitosis was identical in fibroblasts derived from cenpB wild-type, heterozygous and null animals. Our studies demonstrate that CENP-B is not required for the assembly of heterochromatin or the kinetochore, or for completion of mitosis.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9933410     DOI: 10.1007/s004120050343

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  59 in total

1.  Early disruption of centromeric chromatin organization in centromere protein A (Cenpa) null mice.

Authors:  E V Howman; K J Fowler; A J Newson; S Redward; A C MacDonald; P Kalitsis; K H Choo
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-01       Impact factor: 11.205

Review 2.  Establishment of the vertebrate kinetochores.

Authors:  Tetsuya Hori; Tatsuo Fukagawa
Journal:  Chromosome Res       Date:  2012-07       Impact factor: 5.239

Review 3.  Centromeres: long intergenic spaces with adaptive features.

Authors:  Lisa Kanizay; R Kelly Dawe
Journal:  Funct Integr Genomics       Date:  2009-05-12       Impact factor: 3.410

4.  Jerky, a protein deficient in a mouse epilepsy model, is associated with translationally inactive mRNA in neurons.

Authors:  Wencheng Liu; Jeremy Seto; Gerald Donovan; Miklos Toth
Journal:  J Neurosci       Date:  2002-01-01       Impact factor: 6.167

5.  Adaptive evolution of foundation kinetochore proteins in primates.

Authors:  Mary G Schueler; Willie Swanson; Pamela J Thomas; Eric D Green
Journal:  Mol Biol Evol       Date:  2010-02-08       Impact factor: 16.240

Review 6.  The centromere: epigenetic control of chromosome segregation during mitosis.

Authors:  Frederick G Westhorpe; Aaron F Straight
Journal:  Cold Spring Harb Perspect Biol       Date:  2014-11-20       Impact factor: 10.005

Review 7.  Using human artificial chromosomes to study centromere assembly and function.

Authors:  Oscar Molina; Natalay Kouprina; Hiroshi Masumoto; Vladimir Larionov; William C Earnshaw
Journal:  Chromosoma       Date:  2017-07-07       Impact factor: 4.316

Review 8.  Chromatin dynamics during the cell cycle at centromeres.

Authors:  Sebastian Müller; Geneviève Almouzni
Journal:  Nat Rev Genet       Date:  2017-01-31       Impact factor: 53.242

9.  Discovering centromere proteins: from cold white hands to the A, B, C of CENPs.

Authors:  William C Earnshaw
Journal:  Nat Rev Mol Cell Biol       Date:  2015-05-20       Impact factor: 94.444

Review 10.  The unique kind of human artificial chromosome: Bypassing the requirement for repetitive centromere DNA.

Authors:  Craig W Gambogi; Jennine M Dawicki-McKenna; Glennis A Logsdon; Ben E Black
Journal:  Exp Cell Res       Date:  2020-04-01       Impact factor: 3.905

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.