Evidence map›Paper›PMID 19448274›Full record

ArticleGenetics2009

A screen for modifiers of notch signaling uncovers Amun, a protein with a critical role in sensory organ development.

Nevine A Shalaby, Annette L Parks, Eric J Morreale, Marisa C Osswalt, Kristen M Pfau, Eric L Pierce, Marc A T Muskavitch

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Quantifying bristle cell organization inbioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. TheDisease models & mechanisms · 2018
    Article
  7. Review
  8. Discovery of progenitor cell signatures by time-series synexpression analysis during Drosophila embryonic cell immortalization.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Stochastic simulation of notch signaling reveals novel factors that mediate the differentiation of neural stem cells.Journal of computational biology : a journal of computational molecular cell biology · 2014
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Drosophila lilliputian is required for proneural gene expression in retinal development.Developmental dynamics : an official publication of the American Association of Anatomists · 2012
    Article
  19. Article
  20. 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

7 authors at 1 institution in 1 country.

Nevine A ShalabyBiology Department, Boston College, Chestnut Hill, Massachusetts 02467, USA.
Annette L Parks
Eric J Morreale
Marisa C Osswalt
Kristen M Pfau
Eric L Pierce
Marc A T Muskavitch
Boston College · US

Funding

MOLECULAR GENETICS OF NEUROGENESIS IN DROSPHILAR01GM033291 · NIGMS · INDIANA UNIVERSITY BLOOMINGTON · PI MUSKAVITCH, MARC AT · 1985 to 2000
$208k
NIGMS NIH HHS GM33291NIGMS NIH HHS R01 GM033291
6 · The paper itself

Abstract

Notch signaling is an evolutionarily conserved pathway essential for many cell fate specification events during metazoan development. We conducted a large-scale transposon-based screen in the developing Drosophila eye to identify genes involved in Notch signaling. We screened 10,447 transposon lines from the Exelixis collection for modifiers of cell fate alterations caused by overexpression of the Notch ligand Delta and identified 170 distinct modifier lines that may affect up to 274 genes. These include genes known to function in Notch signaling, as well as a large group of characterized and uncharacterized genes that have not been implicated in Notch pathway function. We further analyze a gene that we have named Amun and show that it encodes a protein that localizes to the nucleus and contains a putative DNA glycosylase domain. Genetic and molecular analyses of Amun show that altered levels of Amun function interfere with cell fate specification during eye and sensory organ development. Overexpression of Amun decreases expression of the proneural transcription factor Achaete, and sensory organ loss caused by Amun overexpression can be rescued by coexpression of Achaete. Taken together, our data suggest that Amun acts as a transcriptional regulator that can affect cell fate specification by controlling Achaete levels.

Indexed as

Signal TransductionBasic Helix-Loop-Helix ProteinsDNA GlycosylasesDNA Transposable ElementsDrosophila ProteinsEyeNuclear ProteinsReceptors, NotchSense OrgansTranscription Factorsac protein, DrosophilaAmun protein, DrosophilaBasic Helix-Loop-Helix ProteinsDNA GlycosylasesDNA Transposable ElementsDrosophila ProteinsNuclear ProteinsReceptors, NotchTranscription Factors

Identifiers

PMID19448274
PMCPMC2728848
OpenAlexW2131374845

What Socratic 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 Socratic graph.