Evidence map›Paper›PMID 29099309›Full record

ArticleAutophagy2018

The autophagy-inducing kinases, ULK1 and ULK2, regulate axon guidance in the developing mouse forebrain via a noncanonical pathway.

Bo Wang, Rekha Iyengar, Xiujie Li-Harms, Joung Hyuck Joo, Christopher Wright, Alfonso Lavado, Linda Horner, Mao Yang, Jun-Lin Guan, Sharon Frase and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Physiological functions of ULK1/2.Journal of molecular biology · 2024
    Review
  10. Article
  11. ULK/Atg1: phasing in and out of autophagy.Trends in biochemical sciences · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. Autophagy protein ULK1 interacts with and regulates SARM1 during axonal injury.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Review
  17. Macroautophagy in CNS health and disease.Nature reviews. Neuroscience · 2022
    Review
  18. Article
  19. Article
  20. ULK4 in Neurodevelopmental and Neuropsychiatric Disorders.Frontiers in cell and developmental biology · 2022
    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

13 authors at 4 institutions in 1 country.

Bo Wanga Department of Pathology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Rekha Iyengara Department of Pathology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Xiujie Li-Harmsa Department of Pathology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Joung Hyuck Jooa Department of Pathology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Christopher Wrighta Department of Pathology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Alfonso Lavadob Department of Developmental Neurobiology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Linda Hornerd Cell and Tissue Imaging Center , St. Jude Children's Research Hospital , Memphis , TN , USA.
Mao Yangc Department of Immunology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Jun-Lin Guane Department of Cancer Biology , University of Cincinnati College of Medicine , Cincinnati , OH , USA.
Sharon Frased Cell and Tissue Imaging Center , St. Jude Children's Research Hospital , Memphis , TN , USA.
Douglas R Greenc Department of Immunology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Xinwei Caob Department of Developmental Neurobiology , St. Jude Children's Research Hospital , Memphis , TN , USA.
Mondira Kundua Department of Pathology , St. Jude Children's Research Hospital , Memphis , TN , USA.
St. Jude Children's Research Hospital · USImaging Center · USUniversity of Cincinnati Medical Center · USUniversity of Tennessee Health Science Center · US

Funding

Regulation of autophagy by AMPK, Hsp90-Cdc37 and Ulk1 in erythroid cellsR01HL114697 · NHLBI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KUNDU, MONDIRA · 2012 to 2016
$2.2M
NHLBI NIH HHS R01 HL114697
6 · The paper itself

Abstract

Mammalian ULK1 (unc-51 like kinase 1) and ULK2, Caenorhabditis elegans UNC-51, and Drosophila melanogaster Atg1 are serine/threonine kinases that regulate flux through the autophagy pathway in response to various types of cellular stress. C. elegans UNC-51 and D. melanogaster Atg1 also promote axonal growth and defasciculation; disruption of these genes results in defective axon guidance in invertebrates. Although disrupting ULK1/2 function impairs normal neurite outgrowth in vitro, the role of ULK1 and ULK2 in the developing brain remains poorly characterized. Here, we show that ULK1 and ULK2 are required for proper projection of axons in the forebrain. Mice lacking Ulk1 and Ulk2 in their central nervous systems showed defects in axonal pathfinding and defasciculation affecting the corpus callosum, anterior commissure, corticothalamic axons and thalamocortical axons. These defects impaired the midline crossing of callosal axons and caused hypoplasia of the anterior commissure and disorganization of the somatosensory cortex. The axon guidance defects observed in ulk1/2 double-knockout mice and central nervous system-specific (Nes-Cre) Ulk1/2-conditional double-knockout mice were not recapitulated in mice lacking other autophagy genes (i.e., Atg7 or Rb1cc1 [RB1-inducible coiled-coil 1]). The brains of Ulk1/2-deficient mice did not show stem cell defects previously attributed to defective autophagy in ambra1 (autophagy/Beclin 1 regulator 1)- and Rb1cc1-deficient mice or accumulation of SQSTM1 (sequestosome 1)

Indexed as

AutophagyAxon GuidanceSignal TransductionAnimalsAnimals, NewbornAutophagosomesAutophagy-Related Protein-1 HomologAutophagy-Related Protein 7Autophagy-Related ProteinsAxonsHippocampusIntracellular Signaling Peptides and ProteinsMiceMice, Inbred C57BLMice, KnockoutNeural Stem CellsAutophagy-Related Protein-1 HomologAutophagy-Related Protein 7Autophagy-Related ProteinsIntracellular Signaling Peptides and ProteinsProtein Serine-Threonine KinasesRb1cc1 protein, mouseUbiquitinated ProteinsUlk1 protein, mouseUlk2 protein, mouseATG1ATG7autophagyaxon guidanceneurodevelopmentRB1CC1ULK1/2

Identifiers

PMID29099309
PMCPMC6070005
OpenAlexW2766011561

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.