Transcription by Escherichia coli RNA polymerase (RNAP), a well-characterized member of the multisubunit RNAP family, involves several mechanistic steps inaccessible to methods that study static structures or molecular ensembles. To understand transcription mechanisms, it is necessary to uncover and analyze dynamic, transient, and non-equilibrium steps along the transcription pathway. Single-molecule detection (SMD) is a new set of tools that can stand up to this challenge by monitoring the real-time behavior of individual transcription complexes. We have developed single-molecule Fluorescence Resonance Energy Transfer (smFRET) combined with alternating-laser excitation in order to study the structure and dynamics of transcription complexes. We propose to use this method to understand transcription by analyzing poorly-characterized transitions in transcription complexes; several of these transitions are extremely important for transcriptional regulation, since they form the steps where transcription factors control gene expression. We propose to focus on multistep transitions: the transitions occurring on the path from RNA polymerase to the formation of RNA polymerase-promoter open complex, the transitions occurring on the path from RNA polymerase-promoter open complex to initial transcribing complexes, and transitions occurring on the path from initial transcribing complexes to a mature elongation complex. The results of the proposed work will allow direct observation of structural and mechanistic heterogeneity of transcription complexes; validate or disprove models proposed after decades of genetic, biochemical, and structural analysis of transcription that were not validated experimentally; and will allow generation of real-time, molecular """"""""movies"""""""" of individual, functional RNAP molecules operating on DNA. The high homology of E. coli RNAP polymerase with its eukaryotic counterparts ensures that mechanistic insights obtained from the proposed work will be directly extrapolated to eukaryotic transcription and will greatly enhance understanding of transcription-associated human diseases, such as various forms of cancer, (since numerous oncogenes and tumor-suppressor genes are transcription factors), developmental defects, and other pathological conditions. The proposed methods are applicable to the analysis of nucleoprotein complexes present in DNA replication, DNA recombination, DNA repair, RNA processing and RNA translation, and when combined with advances in site-specific labeling, will allow the study of such processes in living cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM069709-01A1
Application #
6986892
Study Section
Macromolecular Structure and Function C Study Section (MSFC)
Program Officer
Lewis, Catherine D
Project Start
2005-09-01
Project End
2009-08-31
Budget Start
2005-09-01
Budget End
2006-08-31
Support Year
1
Fiscal Year
2005
Total Cost
$449,409
Indirect Cost
Name
University of California Los Angeles
Department
Physiology
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Lerner, Eitan; Cordes, Thorben; Ingargiola, Antonino et al. (2018) Toward dynamic structural biology: Two decades of single-molecule Förster resonance energy transfer. Science 359:
Lerner, Eitan; Ingargiola, Antonino; Weiss, Shimon (2018) Characterizing highly dynamic conformational states: The transcription bubble in RNAP-promoter open complex as an example. J Chem Phys 148:123315
Ingargiola, Antonino; Segal, Maya; Gulinatti, Angelo et al. (2018) 48-spot single-molecule FRET setup with periodic acceptor excitation. J Chem Phys 148:123304
Ingargiola, Antonino; Peronio, Pietro; Lerner, Eitan et al. (2017) 16-Ch Time-resolved Single-Molecule Spectroscopy Using Line Excitation. Proc SPIE Int Soc Opt Eng 10071:
Ingargiola, Antonino; Lerner, Eitan; Chung, SangYoon et al. (2017) Multispot single-molecule FRET: High-throughput analysis of freely diffusing molecules. PLoS One 12:e0175766
Lerner, Eitan; Ingargiola, Antonino; Lee, Jookyung J et al. (2017) Different types of pausing modes during transcription initiation. Transcription 8:242-253
Ingargiola, Antonino; Lerner, Eitan; Chung, SangYoon et al. (2016) FRETBursts: An Open Source Toolkit for Analysis of Freely-Diffusing Single-Molecule FRET. PLoS One 11:e0160716
Lerner, Eitan; Chung, SangYoon; Allen, Benjamin L et al. (2016) Backtracked and paused transcription initiation intermediate of Escherichia coli RNA polymerase. Proc Natl Acad Sci U S A 113:E6562-E6571
Ploetz, Evelyn; Lerner, Eitan; Husada, Florence et al. (2016) Förster resonance energy transfer and protein-induced fluorescence enhancement as synergetic multi-scale molecular rulers. Sci Rep 6:33257
Lerner, Eitan; Ploetz, Evelyn; Hohlbein, Johannes et al. (2016) A Quantitative Theoretical Framework For Protein-Induced Fluorescence Enhancement-Förster-Type Resonance Energy Transfer (PIFE-FRET). J Phys Chem B 120:6401-10

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