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Comparative cell cycle transcriptomics reveals synchronization of developmental transcription factor networks in cancer cells

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    0506873 - BFÚ 2020 RIV US eng J - Journal Article
    Bostrom, J. - Šrámková, Z. - Salasova, A. - Johard, H. - Mahdessian, D. - Fedr, Radek - Marks, C. - Medalová, J. - Souček, Karel - Lundberg, E. - Linnarsson, S. - Bryja, V. - Sekyrová, P. - Altun, M. - Andang, M.
    Comparative cell cycle transcriptomics reveals synchronization of developmental transcription factor networks in cancer cells.
    PLoS ONE. Roč. 12, č. 12 (2017), č. článku e0188772. ISSN 1932-6203. E-ISSN 1932-6203
    R&D Projects: GA ČR(CZ) GA15-11707S; GA MZd(CZ) NV15-28628A; GA MZd(CZ) NV15-33999A
    Institutional support: RVO:68081707
    Keywords : gene-expression * circadian clock * retinoblastoma protein * retinal progenitors
    OECD category: Other biological topics
    Impact factor: 2.766, year: 2017
    Method of publishing: Open access
    https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0188772&type=printable

    The cell cycle coordinates core functions such as replication and cell division. However, cell-cycle-regulated transcription in the control of non-core functions, such as cell identity maintenance through specific transcription factors (TFs) and signalling pathways remains unclear. Here, we provide a resource consisting of mapped transcriptomes in unsynchro-nized HeLa and U2OS cancer cells sorted for cell cycle phase by Fucci reporter expression. We developed a novel algorithm for data analysis that enables efficient visualization and data comparisons and identified cell cycle synchronization of Notch signalling and TFs associated with development. Furthermore, the cell cycle synchronizes with the circadian clock, providing a possible link between developmental transcriptional networks and the cell cycle. In conclusion we find that cell cycle synchronized transcriptional patterns are temporally compartmentalized and more complex than previously anticipated, involving genes, which control cell identity and development.
    Permanent Link: http://hdl.handle.net/11104/0298006

     
     
Number of the records: 1  

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