Probing the target search of DNA-binding proteins in mammalian cells using TetR as model searcher

Autor(en): Normanno, D.
Boudarène, L.
Dugast-Darzacq, C.
Chen, J.
Richter, C.
Proux, F.
Bénichou, O.
Voituriez, R.
Darzacq, X.
Dahan, M.
Stichwörter: DNA-Binding Proteins; Repressor Proteins; tetracycline resistance-encoding transposon repressor protein; cell protein; DNA binding protein; double stranded DNA; DNA binding protein; repressor protein; tetracycline resistance-encoding transposon repressor protein, cell organelle; chemical binding; DNA; mammal; measurement method; molecular analysis; numerical model; protein; quantitative analysis, Article; association rate constant; binding affinity; binding site; bleaching; cell function; chromatin; controlled study; diffusion; DNA binding; DNA sequence; gene cassette; gene locus; human; human cell; human genome; ionic strength; mammal cell; membrane permeability; molecular interaction; osteosarcoma cell; protein DNA binding; protein protein interaction; quantitative analysis; randomized controlled trial; reporter gene; repressor gene; stereospecificity; survival rate; gene expression regulation; genetics; kinetics; metabolism; nucleotide sequence; physiology; protein conformation; protein transport; tumor cell line, Mammalia, Base Sequence; Cell Line, Tumor; DNA-Binding Proteins; Gene Expression Regulation; Humans; Kinetics; Protein Conformation; Protein Transport; Repressor Proteins
Erscheinungsdatum: 2015
Herausgeber: Nature Publishing Group
Journal: Nature Communications
Volumen: 6
Zusammenfassung: 
Many cellular functions rely on DNA-binding proteins finding and associating to specific sites in the genome. Yet the mechanisms underlying the target search remain poorly understood, especially in the case of the highly organized mammalian cell nucleus. Using as a model Tet repressors (TetRs) searching for a multi-array locus, we quantitatively analyse the search process in human cells with single-molecule tracking and single-cell protein-DNA association measurements. We find that TetRs explore the nucleus and reach their target by 3D diffusion interspersed with transient interactions with non-cognate sites, consistent with the facilitated diffusion model. Remarkably, nonspecific binding times are broadly distributed, underlining a lack of clear delimitation between specific and nonspecific interactions. However, the search kinetics is not determined by diffusive transport but by the low association rate to nonspecific sites. Altogether, our results provide a comprehensive view of the recruitment dynamics of proteins at specific loci in mammalian cells. © 2015 Macmillan Publishers Limited. All rights reserved.
ISSN: 20411723
DOI: 10.1038/ncomms8357
Externe URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84936889519&doi=10.1038%2fncomms8357&partnerID=40&md5=19544515835506389ab47fd7c6a14cc6

Show full item record

Page view(s)

2
Last Week
0
Last month
0
checked on May 20, 2024

Google ScholarTM

Check

Altmetric