Literature DB >> 22134836

Comparative analysis of pre-replication complex proteins in transformed and normal cells.

Domenic Di Paola1, Maria Zannis-Hadjopoulos.   

Abstract

This study examines the abundance of the major protein constituents of the pre-replication complex (pre-RC), both genome-wide and in association with specific replication origins, namely the lamin B2, c-myc, 20mer1, and 20mer2 origins. Several pre-RC protein components, namely ORC1-6, Cdc6, Cdt1, MCM4, MCM7, as well as additional replication proteins, such as Ku70/86, 14-3-3, Cdc45, and PCNA, were comparatively and quantitatively analyzed in both transformed and normal cells. The results show that these proteins are overexpressed and more abundantly bound to chromatin in the transformed compared to normal cells. Interestingly, the 20mer1, 20mer2, and c-myc origins exhibited a two- to threefold greater origin activity and a two- to threefold greater in vivo association of the pre-RC proteins with these origins in the transformed cells, whereas the origin associated with the housekeeping lamin B2 gene exhibited both similar levels of activity and in vivo association of these pre-RC proteins in both cell types. Overall, the results indicate that cellular transformation is associated with an overexpression and increased chromatin association of the pre-RC proteins. This study is significant, because it represents the most systematic comprehensive analysis done to date, using multiple replication proteins and different replication origins in both normal and transformed cell lines.
© 2011 Wiley Periodicals, Inc.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22134836     DOI: 10.1002/jcb.24006

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  14 in total

Review 1.  Let's huddle to prevent a muddle: centrosome declustering as an attractive anticancer strategy.

Authors:  A Ogden; P C G Rida; R Aneja
Journal:  Cell Death Differ       Date:  2012-06-01       Impact factor: 15.828

2.  Differential chromatin structure encompassing replication origins in transformed and normal cells.

Authors:  Domenic Di Paola; Emmanouil Rampakakis; Man Kid Chan; Maria Zannis-Hadjopoulos
Journal:  Genes Cancer       Date:  2012-02

3.  Suppression of the DHX9 helicase induces premature senescence in human diploid fibroblasts in a p53-dependent manner.

Authors:  Teresa Lee; Domenic Di Paola; Abba Malina; John R Mills; Amina Kreps; Frank Grosse; Hengli Tang; Maria Zannis-Hadjopoulos; Ola Larsson; Jerry Pelletier
Journal:  J Biol Chem       Date:  2014-07-02       Impact factor: 5.157

4.  Diminished origin-licensing capacity specifically sensitizes tumor cells to replication stress.

Authors:  Kristin M Zimmerman; Rebecca M Jones; Eva Petermann; Penelope A Jeggo
Journal:  Mol Cancer Res       Date:  2013-01-30       Impact factor: 5.852

5.  Estrogen-induced upregulation and 3'-UTR shortening of CDC6.

Authors:  Begum H Akman; Tolga Can; A Elif Erson-Bensan
Journal:  Nucleic Acids Res       Date:  2012-09-12       Impact factor: 16.971

6.  Cdc45 is limiting for replication initiation in humans.

Authors:  Carsten Köhler; Dennis Koalick; Anja Fabricius; Ann Christin Parplys; Kerstin Borgmann; Helmut Pospiech; Frank Grosse
Journal:  Cell Cycle       Date:  2016       Impact factor: 4.534

7.  Cancer cell response to anthracyclines effects: mysteries of the hidden proteins associated with these drugs.

Authors:  Jirina Tyleckova; Rita Hrabakova; Katerina Mairychova; Petr Halada; Lenka Radova; Petr Dzubak; Marian Hajduch; Suresh J Gadher; Hana Kovarova
Journal:  Int J Mol Sci       Date:  2012-11-22       Impact factor: 5.923

8.  Ku protein levels, localization and association to replication origins in different stages of breast tumor progression.

Authors:  Khalil Abdelbaqi; Domenic Di Paola; Emmanouil Rampakakis; Maria Zannis-Hadjopoulos
Journal:  J Cancer       Date:  2013-05-26       Impact factor: 4.207

9.  Monoallelic chromatin conformation flanking long-range silenced domains in cancer-derived and normal cells.

Authors:  Domenic Di Paola; John Raelson; Emmanouil Rampakakis; Mark Basik; Maria Zannis-Hadjopoulos; W Edward C Bradley
Journal:  PLoS One       Date:  2013-05-16       Impact factor: 3.240

10.  Cdc6 cooperates with c-Myc to promote genome instability and epithelial to mesenchymal transition EMT in zebrafish.

Authors:  Ching-Hung Chen; Dar-Shong Lin; Chieh-Wen Cheng; Chun-Ju Lin; Yu-Kang Lo; Chueh-Chuan Yen; Alan Yueh-Luen Lee; Chung-Der Hsiao
Journal:  Oncotarget       Date:  2014-08-15
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.