Evidence map›Paper›PMID 31590586›Full record

ReviewAnnual review of cell and developmental biology2019

Multitasking: Dual Leucine Zipper-Bearing Kinases in Neuronal Development and Stress Management.

Yishi Jin, Binhai Zheng

Open access · greenAbstract readReview
In one paragraph

Review in Annual review of cell and developmental biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

32 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. A tubulin-MAPKKK pathway engages tubulin isotype interaction for neuroprotection.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Stathmin-2 enhances motor axon regeneration after injury independent of its binding to tubulin.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Genes in Axonal Regeneration.Molecular neurobiology · 2024
    Review
  14. Context-Specific Stress Causes Compartmentalized SARM1 Activation and Local Degeneration in Cortical Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. An intraflagellar transport dependent negative feedback regulates the MAPKKK DLK-1 to protect cilia from degeneration.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  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

2 authors at 2 institutions in 1 country.

Yishi JinNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, California 92093, USA; email: yijin@ucsd.edu.
Binhai ZhengDepartment of Neurosciences, School of Medicine, University of California, San Diego, La Jolla, California 92093, USA; email: bizheng@ucsd.edu.
University of California, San Diego · USVA San Diego Healthcare System · US

Funding

U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
The Role of a Pair of MAP3Ks in the Multicellular Response to Spinal Cord InjuryR01NS093055 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHENG, BINHAI · 2015 to 2024
$4.0M
Cytoskeletal dynamics in axon regenerationR01NS093588 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHISHOLM, ANDREW D, JIN, YISHI · 2015 to 2023
$3.7M
GABAergic Neuron Differentiation in C.elegansR37NS035546 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JIN, YISHI · 2017 to 2021
$2.4M
Harnessing Corticospinal Axon Sprouting for Functional Recovery in Chronic InjuryI01RX002483 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI ZHENG, BINHAI · 2019 to 2023
–
NINDS NIH HHS P30 NS047101NINDS NIH HHS R01 NS093055NINDS NIH HHS R01 NS093588NINDS NIH HHS R37 NS035546RRD VA I01 RX002483
6 · The paper itself

Abstract

The dual leucine zipper-bearing kinase (DLK) and leucine zipper-bearing kinase (LZK) are evolutionarily conserved MAPKKKs of the mixed-lineage kinase family. Acting upstream of stress-responsive JNK and p38 MAP kinases, DLK and LZK have emerged as central players in neuronal responses to a variety of acute and traumatic injuries. Recent studies also implicate their function in astrocytes, microglia, and other nonneuronal cells, reflecting their expanding roles in the multicellular response to injury and in disease. Of particular note is the potential link of these kinases to neurodegenerative diseases and cancer. It is thus critical to understand the physiological contexts under which these kinases are activated, as well as the signal transduction mechanisms that mediate specific functional outcomes. In this review we first provide a historical overview of the biochemical and functional dissection of these kinases. We then discuss recent findings on regulating their activity to enhance cellular protection following injury and in disease, focusing on but not limited to the nervous system.

Indexed as

AnimalsAxonsHumansLeucine ZippersMAP Kinase Kinase KinasesNeurodegenerative DiseasesNeurogliaNeuronsRegenerationStem CellsStress, PhysiologicalWounds and InjuriesMAP3K13 protein, humanMAP Kinase Kinase Kinasesmitogen-activated protein kinase kinase kinase 12adipogenesisAlzheimer disease modelsastrocytesaxon degenerationaxon regenerationcytoskeletonDLKDLK-1HSV infectioninsulin β-cellsJNKLZKMAP3Kneuronal deathneuronal developmentp38Wallenda

Identifiers

PMID31590586
PMCPMC7015696
OpenAlexW2980183421

What OpenQuestion holds

Textmetadata
LicenceTDM
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.