Evidence map›Paper›PMID 25776889›Full record

ArticleMolecular & cellular proteomics : MCP2015

The Drosophila Helicase Maleless (MLE) is Implicated in Functions Distinct From its Role in Dosage Compensation.

Simona Cugusi, Satish Kallappagoudar, Huiping Ling, John C Lucchesi

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Multifunctional ENY2 Protein Interacts with RNA Helicase MLE.Doklady. Biochemistry and biophysics · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. The essential Drosophila CLAMP protein differentially regulates non-coding roX RNAs in male and females.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2017
    Article
  11. Article
  12. 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

4 authors at 1 institution in 1 country.

Simona CugusiFrom the ‡Department of Biology, Emory University, Atlanta, Georgia 30322.
Satish KallappagoudarFrom the ‡Department of Biology, Emory University, Atlanta, Georgia 30322.
Huiping LingFrom the ‡Department of Biology, Emory University, Atlanta, Georgia 30322.
John C LucchesiFrom the ‡Department of Biology, Emory University, Atlanta, Georgia 30322 jclucch@emory.edu.
Emory University · US

Funding

Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Luiz Eduardo Bertassoni · 1997 to 2026
$60.5M
Proteomics CoreP30EY010572 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TED S ACOTT · 1995 to 2026
$19.4M
Hair-Bundle ProteinsR01DC002368 · NIDCD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Peter Gordon Barr-Gillespie · 1994 to 2026
$11.3M
GENETIC REGULATION IN DROSOPHILA: DOSAGE COMPENSATIONR01GM015691 · NIGMS · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI LUCCHESI, JOHN · 1985 to 2012
$4.8M
LTQ Orbitrap VelosS10OD012246 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI DAVID, LARRY L · 2012 to 2012
$854k
LTQ XL Linear Ion Trap Mass SpectrometerS10RR025571 · NCRR · OREGON HEALTH & SCIENCE UNIVERSITY · PI DAVID, LARRY L · 2009 to 2009
$389k
NCI NIH HHS P30 CA069533NCI NIH HHS P30CA069533NCRR NIH HHS S10 RR025571NCRR NIH HHS S10RR025571NEI NIH HHS P30 EY010572NEI NIH HHS P30EY010572NIDCD NIH HHS R01 DC002368NIDCD NIH HHS R01DC002368-15S1NIGMS NIH HHS GM15691NIGMS NIH HHS R01 GM015691NIH HHS S10 OD012246NIH HHS S10OD012246
6 · The paper itself

Abstract

Helicases are ubiquitous enzymes that unwind or remodel single or double-stranded nucleic acids, and that participate in a vast array of metabolic pathways. The ATP-dependent DEXH-box RNA/DNA helicase MLE was first identified as a core member of the chromatin remodeling MSL complex, responsible for dosage compensation in Drosophila males. Although this complex does not assemble in females, MLE is present. Given the multiplicity of functions attributed to its mammalian ortholog RNA helicase A, we have carried out an analysis for the purpose of determining whether MLE displays the same diversity. We have identified a number of different proteins that associate with MLE, implicating its role in specific pathways. We have documented this association in selected examples that include the spliceosome complex, heterogeneous Nuclear Ribonucleoproteins involved in RNA Processing and in Heterochromatin Protein 1 deposition, and the NuRD complex.

Indexed as

AnimalsCell LineChromosomal Proteins, Non-HistoneDNA HelicasesDosage Compensation, GeneticDrosophilaDrosophila ProteinsMi-2 Nucleosome Remodeling and Deacetylase ComplexSpliceosomesTranscription FactorsChromosomal Proteins, Non-HistoneDNA HelicasesDrosophila Proteinsheterochromatin protein 1, DrosophilaMi-2 Nucleosome Remodeling and Deacetylase Complexmle protein, DrosophilaTranscription Factors

Identifiers

PMID25776889
PMCPMC4458714
OpenAlexW1994788630

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.