Evidence map›Paper›PMID 29514105›Full record

ArticleCell reports2018

Fine-Resolution Mapping of TF Binding and Chromatin Interactions.

Jenia Gutin, Ronen Sadeh, Nitzan Bodenheimer, Daphna Joseph-Strauss, Avital Klein-Brill, Adi Alajem, Oren Ram, Nir Friedman

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 57 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Jenia GutinSchool of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel; Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Ronen SadehSchool of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel; Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel. Electronic address: ronensadeh@gmail.com.
Nitzan BodenheimerSchool of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel; Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Daphna Joseph-StraussSchool of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel; Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Avital Klein-BrillSchool of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel; Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Adi AlajemInstitute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Oren RamInstitute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.
Nir FriedmanSchool of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel; Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel. Electronic address: nir.friedman@mail.huji.ac.il.
Hebrew University of Jerusalem · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcription factor (TF) binding to DNA is crucial for transcriptional regulation. There are multiple methods for mapping such binding. These methods balance between input requirements, spatial resolution, and compatibility with high-throughput automation. Here, we describe SLIM-ChIP (short-fragment-enriched, low-input, indexed MNase ChIP), which combines enzymatic fragmentation of chromatin and on-bead indexing to address these desiderata. SLIM-ChIP reproduces a high-resolution binding map of yeast Reb1 comparable with existing methods, yet with less input material and full compatibility with high-throughput procedures. We demonstrate the robustness and flexibility of SLIM-ChIP by probing additional factors in yeast and mouse. Finally, we show that SLIM-ChIP provides information on the chromatin landscape surrounding the bound transcription factor. We identify a class of Reb1 sites where the proximal -1 nucleosome tightly interacts with Reb1 and maintains unidirectional transcription. SLIM-ChIP is an attractive solution for mapping DNA binding proteins and charting the surrounding chromatin occupancy landscape at a single-cell level.

Indexed as

AnimalsBase SequenceCell LineChromatinChromatin ImmunoprecipitationGenomeMiceNucleosomesPromoter Regions, GeneticProtein BindingSaccharomyces cerevisiaeTranscription FactorsTranscription Initiation, GeneticChromatinNucleosomesTranscription FactorsChIP-seqchromatinCTCFDNA-bindingnucleosomespromoter directionalityReb1transcription factor

Identifiers

PMID29514105
PMCPMC5863041
OpenAlexW2793270492

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.