@article{fb3e2aab70f5401ba377c928f0c9e073,
title = "Palladin is a neuron-specific translational target of mtor signaling that regulates axon morphogenesis",
abstract = "The mTOR signaling pathway regulates protein synthesis and diverse aspects of neuronal morphology that are important for brain development and function. To identify proteins controlled translationally by mTOR signaling, we performed ribosome profiling analyses in mouse cortical neurons and embryonic stem cells upon acute mTOR inhibition. Among proteins whose translation was significantly affected by mTOR inhibition selectively in neurons, we identified the cytoskeletal regulator protein palladin, which is localized within the cell body and axons in hippocampal neurons. Knockdown of palladin eliminated supernumerary axons induced by suppression of the tuberous sclerosis complex protein TSC1 in neurons, demonstrating that palladin regulates neuronal morphogenesis downstream of mTOR signaling. Our findings provide novel insights into an mTOR-dependent mechanism that controls neuronal morphogenesis through translational regulation.",
keywords = "Axon, Palladin, Ribosome, Translation",
author = "Yusuke Umegaki and Brotons, {Antonio Mart{\'i}nez} and Yui Nakanishi and Zhongyue Luo and Hanlu Zhang and Azad Bonni and Yoshiho Ikeuchi",
note = "Funding Information: This work was supported by Japan Society for the Promotion of Science (JSPS) Grants-in-Aid for Scientific Research26890008,15K14311,15H01528,and17H05661(Y.I.),UeharaMemorialFoundation(Y.I.),MochidaMemo-rial Foundation (Y.I.), Mathers Foundation (A.B.), and NIH Grant NS051255 (A.B.). We thank Shintaro Iwasaki and Jagat Chhipishrestha for critical discussion and providing PP242; Luis de la Torre-Ubieta, Luis Mejia, and Anna Oldenborg for providing support for plasmids used in the study; the Genome Technology Access Center in the DepartmentofGeneticsatWashingtonUniversitySchoolofMedicineforhelpwithsequencinganalyses;computing resource was provided by Human Genome Center, the Institute of Medical Science, the University of Tokyo; pSpCas9(BB)-2A-Puro(pX459)V2.0wasagiftfromFengZhang(Addgeneplasmid#62988);andtheSAD-Aexpres-sion plasmid was a gift from Josh Sanes. The authors declare no competing financial interests. Publisher Copyright: {\textcopyright} 2018 the authors.",
year = "2018",
month = may,
day = "23",
doi = "10.1523/JNEUROSCI.2370-17.2018",
language = "English",
volume = "38",
pages = "4985--4995",
journal = "Journal of Neuroscience",
issn = "0270-6474",
number = "21",
}