Evidence map›Paper›PMID 11825878›Full record

ArticleGenes & development2002

Activation of the JNK pathway during dorsal closure in Drosophila requires the mixed lineage kinase, slipper.

Beth Stronach, Norbert Perrimon

Open access · diamondAbstract readComparative Study
In one paragraph

Article in Genes & development, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed, 109 citations in OpenAlex.

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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.

Beth StronachDepartment of Genetics, Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
Norbert Perrimon
Harvard University · USHoward Hughes Medical Institute · US

Funding

SIGNALING CELL MOVEMENT IN DORSAL CLOSUREF32GM019775 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI STRONACH, BETH E · 1999 to 2001
$80k
NIGMS NIH HHS F32 GM019775NIGMS NIH HHS GM19775
6 · The paper itself

Abstract

The Jun kinase (JNK) pathway has been characterized for its role in stimulating AP-1 activity and for modulating the balance between cell growth and death during development, inflammation, and cancer. Six families of mammalian kinases acting at the level of JNKKK have emerged as upstream regulators of JNK activity (MLK, LZK, TAK, ASK, MEKK, and TPL); however, the specificity underlying which kinase is utilized for transducing a distinct signal is poorly understood. In Drosophila, JNK signaling plays a central role in dorsal closure, controlling cell fate and cell sheet morphogenesis during embryogenesis. Notably, in the fly genome, there are single homologs of each of the mammalian JNKKK families. Here, we identify mutations in one of those, a mixed lineage kinase, named slipper (slpr), and show that it is required for JNK activation during dorsal closure. Furthermore, our results show that other putative JNKKKs cannot compensate for the loss of slpr function and, thus, may regulate other JNK or MAPK-dependent processes.

Indexed as

Drosophila ProteinsJNK Mitogen-Activated Protein KinasesAmino Acid SequenceAnimalsCell PolarityCloning, MolecularDrosophilaFemaleGene Expression Regulation, DevelopmentalHumansMaleMAP Kinase Kinase 4MAP Kinase Kinase 7MAP Kinase Kinase KinasesMitogen-Activated Protein Kinase Kinase Kinase 11Mitogen-Activated Protein Kinase KinasesDrosophila ProteinsJNK Mitogen-Activated Protein KinasesMAP2K7 protein, humanMAP3K10 protein, humanMAP3K9 protein, humanMAP Kinase Kinase 4MAP Kinase Kinase 7MAP Kinase Kinase KinasesMitogen-Activated Protein Kinase Kinase Kinase 11Mitogen-Activated Protein Kinase Kinasesslpr protein, Drosophila

Identifiers

PMID11825878
PMCPMC155330
OpenAlexW2139172604

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.