Evidence map›Paper›PMID 28336073›Full record

ArticleMethods in enzymology2017

Visualization of the Genomic Loci That Are Bound by Specific Multiprotein Complexes by Bimolecular Fluorescence Complementation Analysis on Drosophila Polytene Chromosomes.

Huai Deng, Tom K Kerppola

Abstract read
In one paragraph

Article in Methods in enzymology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Huai DengUniversity of Michigan, Ann Arbor, MI, United States.
Tom K KerppolaUniversity of Michigan, Ann Arbor, MI, United States. Electronic address: kerppola@umich.edu.
University of Michigan–Ann Arbor · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Optimization of Bimolecular Fluorescence Complementation Probes for New Imaging FR01GM086213 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KERPPOLA, TOM KLAUS, REDDY, KAREN LYNN · 2008 to 2011
$2.8M
Visualization of Combinatorial Epigenetic Marks and Complexes in Animals Using FlR01DA030339 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KERPPOLA, TOM KLAUS · 2010 to 2016
$1.7M
NIDA NIH HHS R01 DA030339NIDDK NIH HHS P30 DK020572NIGMS NIH HHS R01 GM086213
6 · The paper itself

Abstract

We have developed a procedure that enables visualization of the genomic loci that are bound by complexes formed by a specific combination of chromatin-binding proteins. This procedure is based on imaging bimolecular fluorescence complementation (BiFC) complexes on Drosophila polytene chromosomes. BiFC complexes are formed by the facilitated association of two fluorescent protein fragments that are fused to proteins that interact with, or are in close proximity to, each other. The intensity of BiFC complex fluorescence at individual genomic loci is greatly enhanced by the parallel alignment of hundreds of chromatids within the polytene chromosomes. The loci that are bound by the complexes are mapped by comparing the locations of BiFC complex fluorescence with the stereotypical banding patterns of the chromosomes. We describe strategies for the design, expression, and validation of fusion proteins for the analysis of BiFC complex binding on polytene chromosomes. We detail protocols for the preparation of polytene chromosome spreads that have been optimized for the purpose of BiFC complex visualization. Finally, we provide guidance for the interpretation of results from studies of BiFC complex binding on polytene chromosomes and for comparison of the genomic loci that are bound by BiFC complexes with those that are bound by subunits of the corresponding endogenous complexes. The visualization of BiFC complex binding on polytene chromosomes provides a unique method to visualize multiprotein complex binding at specific loci, throughout the genome, in individual cells.

Indexed as

Genetic LociAnimalsDrosophilaDrosophila ProteinsLuminescent ProteinsMicroscopy, FluorescenceMultiprotein ComplexesOptical ImagingPolytene ChromosomesRecombinant Fusion ProteinsDrosophila ProteinsLuminescent ProteinsMultiprotein ComplexesRecombinant Fusion ProteinsBiFC complex imagingChromatin binding proteinsFluorescent protein fragmentsGenomewide analysisPolytene chromosome spreadsTranscription factor interactionTransgene expression in specific tissues

Identifiers

PMID28336073
PMCPMC5542922
OpenAlexW2594483382

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.