Abstract
To maintain phenotypes of cell lineages, cells must 'remember' which genes were active before mitosis entry and transmit this information to their daughter cells so that expression patterns can be faithfully re-established in G1. This phenomenon is called gene bookmarking. However, during mitosis transcription ceases, most sequence-specific proteins dissociate from DNA and the chromatin is tightly compacted, making it difficult to understand how gene activity 'memory' is maintained through this stage of the cell cycle. A feature of gene bookmarking is that in mitotic cells, the promoters of formerly active genes lack compaction, but how compaction of these regions is inhibited is unknown. Here we show that during mitosis, TATA-binding protein (TBP), which remains bound to DNA during mitosis, recruits PP2A. TBP also interacts with condensin to allow efficient dephosphorylation and inactivation of condensin near these promoters to inhibit their compaction. Further, ChIP-on-chip data show that TBP is bound to many chromosomal sites during mitosis, and is higher in transcribed regions but low in regions containing pseudogenes and genes whose expression is tissue-restricted. These results suggest that TBP is involved not only in gene transcription during interphase but also in preserving the memory of gene activity through mitosis to daughter cells.
MeSH Terms
Adenosine Triphosphatases/metabolism
DNA-Binding Proteins/metabolism
Escherichia coli/genetics
Genes
Glutathione Transferase/metabolism
HeLa Cells
Humans
Mitosis
Multiprotein Complexes/metabolism
Protein Phosphatase 2/genetics,metabolism
RNA, Small Interfering/pharmacology
Recombinant Proteins/metabolism
TATA-Box Binding Protein/genetics,metabolism
Chemicals
DNA-Binding Proteins
Multiprotein Complexes
RNA, Small Interfering
Recombinant Proteins
TATA-Box Binding Protein
condensin complexes
Glutathione Transferase
PPP2CA protein, human
Protein Phosphatase 2
Adenosine Triphosphatases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Xing Hongyan
Department of Molecular and Cellular Biochemistry, Chandler Medical Center, University of Kentucky, Lexington, KY 40536, USA.
Vanderford Nathan L
Sarge Kevin D
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