Evidence map›Paper›PMID 28654043›Full record

ArticleJournal of visualized experiments : JoVE2017

Light-mediated Reversible Modulation of the Mitogen-activated Protein Kinase Pathway during Cell Differentiation and Xenopus Embryonic Development.

Vishnu V Krishnamurthy, Aurora J Turgeon, John S Khamo, Payel Mondal, Savanna R Sharum, Wenyan Mei, Jing Yang, Kai Zhang

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

8 authors.

Vishnu V KrishnamurthyDepartment of Biochemistry, University of Illinois at Urbana-Champaign.
Aurora J TurgeonDepartment of Comparative Biosciences, University of Illinois at Urbana-Champaign.
John S KhamoDepartment of Biochemistry, University of Illinois at Urbana-Champaign.
Payel MondalDepartment of Biochemistry, University of Illinois at Urbana-Champaign.
Savanna R SharumDepartment of Biochemistry, University of Illinois at Urbana-Champaign.
Wenyan MeiDepartment of Comparative Biosciences, University of Illinois at Urbana-Champaign.
Jing YangDepartment of Comparative Biosciences, University of Illinois at Urbana-Champaign; yangj@illinois.edu.
Kai ZhangDepartment of Biochemistry, University of Illinois at Urbana-Champaign; Neuroscience Program, University of Illinois at Urbana-Champaign; Center for Biophysics and Quantitative Biology, University of Illinois at Urbana-Champaign; kaizkaiz@illinois.edu.

Funding

Maternal control of germline developmentR35GM131810 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI Jing Yang · 2019 to 2026
$3.2M
Dnd1 and repression of transcription in primordial germ cellsR01GM111816 · NIGMS · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI YANG, JING · 2015 to 2018
$1.2M
NIGMS NIH HHS R01 GM111816NIGMS NIH HHS R35 GM131810
6 · The paper itself

Abstract

Kinase activity is crucial for a plethora of cellular functions, including cell proliferation, differentiation, migration, and apoptosis. During early embryonic development, kinase activity is highly dynamic and widespread across the embryo. Pharmacological and genetic approaches are commonly used to probe kinase activities. Unfortunately, it is challenging to achieve superior spatial and temporal resolution using these strategies. Furthermore, it is not feasible to control the kinase activity in a reversible fashion in live cells and multicellular organisms. Such a limitation remains a bottleneck for achieving a quantitative understanding of kinase activity during development and differentiation. This work presents an optogenetic strategy that takes advantage of a bicistronic system containing photoactivatable proteins Arabidopsis thaliana cryptochrome 2 (CRY2) and the N-terminal domain of cryptochrome-interacting basic-helix-loop-helix (CIBN). Reversible activation of the mitogen-activated protein kinase (MAPK) signaling pathway is achieved through light-mediated protein translocation in live cells. This approach can be applied to mammalian cell cultures and live vertebrate embryos. This bicistronic system can be generalized to control the activity of other kinases with similar activation mechanisms and can be applied to other model systems.

Indexed as

LightAnimalsArabidopsis ProteinsCell DifferentiationCricetinaeEmbryonic DevelopmentEmbryo, NonmammalianMitogen-Activated Protein KinasesOptogeneticsProtein TransportSignal TransductionXenopusArabidopsis ProteinsMitogen-Activated Protein Kinases

Identifiers

PMID28654043
PMCPMC5608446

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.