Evidence map›Paper›PMID 11687630›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Cell-type specificity of short-range transcriptional repressors.

J R Ryu, L K Olson, D N Arnosti

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. The gap gene network.Cellular and molecular life sciences : CMLS · 2011
    Review
  4. Article
  5. The TetR family of transcriptional repressors.Microbiology and molecular biology reviews : MMBR · 2005
    Review
  6. Article
  7. Article
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

3 authors at 1 institution in 1 country.

J R RyuDepartment of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824-1319, USA.
L K Olson
D N Arnosti
Michigan State University · US

Funding

MOLECULAR ANALYSIS OF TRANSCRIPTIONAL REPRESSIONR01GM056976 · NIGMS · MICHIGAN STATE UNIVERSITY · PI ARNOSTI, DAVID N · 1998 to 2014
$4.7M
NIGMS NIH HHS GM56976NIGMS NIH HHS R01 GM056976
6 · The paper itself

Abstract

Transcriptional repressors can be classified as short- or long-range, according to their range of activity. Functional analysis of identified short-range repressors has been carried out largely in transgenic Drosophila, but it is not known whether general properties of short-range repressors are evident in other types of assays. To study short-range transcriptional repressors in cultured cells, we created chimeric tetracycline repressors based on Drosophila transcriptional repressors Giant, Drosophila C-terminal-binding protein (dCtBP), and Knirps. We find that Giant and dCtBP are efficient repressors in Drosophila and mammalian cells, whereas Knirps is active only in insect cells. The restricted activity of Knirps, in contrast to that of Giant, suggests that not all short-range repressors possess identical activities, consistent with recent findings showing that short-range repressors act through multiple pathways. The mammalian repressor Kid is more effective than either Giant or dCtBP in mammalian cells but is inactive in Drosophila cells. These results indicate that species-specific factors are important for the function of the Knirps and Kid repressors. Giant and dCtBP repress reporter genes in a variety of contexts, including genes that were introduced by transient transfection, carried on episomal elements, or stably integrated. This broad activity indicates that the context of the target gene is not critical for the ability of short-range repressors to block transcription, in contrast to other repressors that act only on stably integrated genes.

Indexed as

AnimalsBase SequenceDNA PrimersDrosophilaHeLa CellsHerpes Simplex Virus Protein Vmw65HumansPromoter Regions, GeneticRecombinant ProteinsRepressor ProteinsDNA PrimersHerpes Simplex Virus Protein Vmw65Recombinant ProteinsRepressor Proteinstetracycline resistance-encoding transposon repressor protein

Identifiers

PMID11687630
PMCPMC60807
OpenAlexW2059434266

What OpenQuestion holds

Textmetadata
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.