Evidence map›Paper›PMID 21205799›Full record

ArticleDevelopment (Cambridge, England)2011

Sugar-free frosting, a homolog of SAD kinase, drives neural-specific glycan expression in the Drosophila embryo.

Sarah Baas, Mary Sharrow, Varshika Kotu, Meg Middleton, Khoi Nguyen, Heather Flanagan-Steet, Kazuhiro Aoki, Michael Tiemeyer

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Changes in Presynaptic Gene Expression during Homeostatic Compensation at a Central Synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  5. Serum N-Glycome Diversity in Teleost and Chondrostrean Fishes.Frontiers in molecular biosciences · 2021
    Article
  6. Article
  7. Article
  8. Review
  9. COG7 deficiency inJournal of cell science · 2017
    Article
  10. Bridging the Gap between Glycosylation and Vesicle Traffic.Frontiers in cell and developmental biology · 2016
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. SAD kinases control the maturation of nerve terminals in the mammalian peripheral and central nervous systems.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  16. Review
  17. Article
  18. Article
  19. Vertebrate protein glycosylation: diversity, synthesis and function.Nature reviews. Molecular cell biology · 2012
    Review
  20. 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

8 authors.

Sarah BaasComplex Carbohydrate Research Center, University of Georgia, 315 Riverbend Road, Athens, GA 30602-4712, USA.
Mary Sharrow
Varshika Kotu
Meg Middleton
Khoi Nguyen
Heather Flanagan-Steet
Kazuhiro Aoki
Michael Tiemeyer

Funding

Mechanisms regulating glycan expression and functionR01GM072839 · NIGMS · UNIVERSITY OF GEORGIA (UGA) · PI TIEMEYER, MICHAEL · 2005 to 2008
$1.1M
NIGMS NIH HHS GM072839NIGMS NIH HHS R01 GM072839
6 · The paper itself

Abstract

Precise glycan structures on specific glycoproteins impart functionalities essential for neural development. However, mechanisms controlling embryonic neural-specific glycosylation are unknown. A genetic screen for relevant mutations in Drosophila generated the sugar-free frosting (sff) mutant that reveals a new function for protein kinases in regulating substrate flux through specific Golgi processing pathways. Sff is the Drosophila homolog of SAD kinase, which regulates synaptic vesicle tethering and neuronal polarity in nematodes and vertebrates. Our Drosophila sff mutant phenotype has features in common with SAD kinase mutant phenotypes in these other organisms, but we detect altered neural glycosylation well before the initiation of embryonic synaptogenesis. Characterization of Golgi compartmentation markers indicates altered colocalization that is consistent with the detected shift in glycan complexity in sff mutant embryos. Therefore, in analogy to synaptic vesicle tethering, we propose that Sff regulates vesicle tethering at Golgi membranes in the developing Drosophila embryo. Furthermore, neuronal sff expression is dependent on transcellular signaling through a non-neural toll-like receptor, linking neural-specific glycan expression to a kinase activity that is induced in response to environmental cues.

Indexed as

AnimalsChromatography, LiquidDrosophilaDrosophila ProteinsEmbryo, NonmammalianGlycosylationGolgi ApparatusImmunohistochemistryIn Situ HybridizationIntracellular MembranesMicroscopy, ConfocalPolysaccharidesReverse Transcriptase Polymerase Chain ReactionTandem Mass SpectrometryDrosophila ProteinsPolysaccharides

Identifiers

PMID21205799
PMCPMC3014640

What OpenQuestion holds

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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.