A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä

A simple optogenetic MAPK inhibitor design reveals resonance between transcription-regulating circuitry and temporally-encoded inputs




Tekijätde Mera RMMF, Li LL, Popinigis A, Cisek K, Tuittila M, Yadav L, Serva A, Courtney MJ

KustantajaNATURE PUBLISHING GROUP

Julkaisuvuosi2017

JournalNature Communications

Tietokannassa oleva lehden nimiNATURE COMMUNICATIONS

Lehden akronyymiNAT COMMUN

Artikkelin numeroARTN 15017

Vuosikerta8

Sivujen määrä18

ISSN2041-1723

eISSN2041-1723

DOIhttps://doi.org/10.1038/ncomms15017

Verkko-osoitehttp://www.nature.com/articles/ncomms15017

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/24961009


Tiivistelmä
Engineering light-sensitive protein regulators has been a tremendous multidisciplinary challenge. Optogenetic regulators of MAPKs, central nodes of cellular regulation, have not previously been described. Here we present OptoJNKi, a light-regulated JNK inhibitor based on the AsLOV2 light-sensor domain using the ubiquitous FMN chromophore. OptoJNKi genetransfer allows optogenetic applications, whereas protein delivery allows optopharmacology. Development of OptoJNKi suggests a design principle for other optically regulated inhibitors. From this, we generate Optop38i, which inhibits p38MAPK in intact illuminated cells. Neurons are known for interpreting temporally-encoded inputs via interplay between ion channels, membrane potential and intracellular calcium. However, the consequences of temporal variation of JNK-regulating trophic inputs, potentially resulting from synaptic activity and reversible cellular protrusions, on downstream targets are unknown. Using OptoJNKi, we reveal maximal regulation of c-Jun transactivation can occur at unexpectedly slow periodicities of inhibition depending on the inhibitor's subcellular location. This provides evidence for resonance in metazoan JNK-signalling circuits.

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