Evidence map›Paper›PMID 25326235›Full record

ArticleGenetics2014

Epigenetic control of learning and memory in Drosophila by Tip60 HAT action.

Songjun Xu, Rona Wilf, Trisha Menon, Priyalakshmi Panikker, Jessica Sarthi, Felice Elefant

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.7field-weighted citation impact, top 19% 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

37 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Tip60's Novel RNA-Binding Function Modulates Alternative Splicing of Pre-mRNA Targets Implicated in Alzheimer's Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  13. Article
  14. Article
  15. Epigenetics in Alzheimer's Disease.Frontiers in aging neuroscience · 2022
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Epigenetic regulation of post-embryonic development.Current opinion in insect science · 2021
    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

6 authors at 1 institution in 1 country.

Songjun XuDepartment of Biology, Drexel University, Philadelphia, Pennsylvania 19104.
Rona WilfDepartment of Biology, Drexel University, Philadelphia, Pennsylvania 19104.
Trisha MenonDepartment of Biology, Drexel University, Philadelphia, Pennsylvania 19104.
Priyalakshmi PanikkerDepartment of Biology, Drexel University, Philadelphia, Pennsylvania 19104.
Jessica SarthiDepartment of Biology, Drexel University, Philadelphia, Pennsylvania 19104.
Felice ElefantDepartment of Biology, Drexel University, Philadelphia, Pennsylvania 19104 fe22@drexel.edu.
Drexel University · US

Funding

TIP60 and APP in Neuronal DevelopmentR01HD057939 · NICHD · DREXEL UNIVERSITY · PI ELEFANT, FELICE · 2008 to 2012
$1.2M
NICHD NIH HHS R01 HD057939NICHD NIH HHS R01HD057939
6 · The paper itself

Abstract

Disruption of epigenetic gene control mechanisms in the brain causes significant cognitive impairment that is a debilitating hallmark of most neurodegenerative disorders, including Alzheimer's disease (AD). Histone acetylation is one of the best characterized of these epigenetic mechanisms that is critical for regulating learning- and memory- associated gene expression profiles, yet the specific histone acetyltransferases (HATs) that mediate these effects have yet to be fully characterized. Here, we investigate an epigenetic role for the HAT Tip60 in learning and memory formation using the Drosophila CNS mushroom body (MB) as a well-characterized cognition model. We show that Tip60 is endogenously expressed in the Kenyon cells, the intrinsic neurons of the MB, and in the MB axonal lobes. Targeted loss of Tip60 HAT activity in the MB causes thinner and shorter axonal lobes while increasing Tip60 HAT levels cause no morphological defects. Functional consequences of both loss and gain of Tip60 HAT levels in the MB are evidenced by defects in immediate-recall memory. Our ChIP-Seq analysis reveals that Tip60 target genes are enriched for functions in cognitive processes, and, accordingly, key genes representing these pathways are misregulated in the Tip60 HAT mutant fly brain. Remarkably, we find that both learning and immediate-recall memory deficits that occur under AD-associated, amyloid precursor protein (APP)-induced neurodegenerative conditions can be effectively rescued by increasing Tip60 HAT levels specifically in the MB. Together, our findings uncover an epigenetic transcriptional regulatory role for Tip60 in cognitive function and highlight the potential of HAT activators as a therapeutic option for neurodegenerative disorders.

Indexed as

Epigenesis, GeneticLearningMemoryAnimalsBrainCell LineDisease Models, AnimalDrosophilaDrosophila ProteinsEnzyme ActivationGene ExpressionGene Expression Regulation, DevelopmentalHistone AcetyltransferasesMushroom BodiesNeurodegenerative DiseasesNeuronsDrosophila ProteinsHistone AcetyltransferasesTip60 protein, DrosophilacognitionDrosophilaepigeneticshistone acetylationTip60

Identifiers

PMID25326235
PMCPMC4256772
OpenAlexW2002524846

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.