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The zinc finger/RING domain protein Unkempt regulates cognitive flexibility
Correct orchestration of nervous system development is a profound challenge that involves coordination of complex molecular and cellular processes. Mechanistic target of rapamycin (mTOR) signaling is a key regulator of nervous system development and synaptic function. The mTOR kinase is a hub for se...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357790/ https://www.ncbi.nlm.nih.gov/pubmed/34381067 http://dx.doi.org/10.1038/s41598-021-95286-y |
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author | Vinsland, Elin Baskaran, Pranetha Mihaylov, Simeon R. Hobbs, Carl Wood, Hannah Bouybayoune, Ihssane Shah, Kriti Houart, Corinne Tee, Andrew R. Murn, Jernej Fernandes, Cathy Bateman, Joseph M. |
author_facet | Vinsland, Elin Baskaran, Pranetha Mihaylov, Simeon R. Hobbs, Carl Wood, Hannah Bouybayoune, Ihssane Shah, Kriti Houart, Corinne Tee, Andrew R. Murn, Jernej Fernandes, Cathy Bateman, Joseph M. |
author_sort | Vinsland, Elin |
collection | PubMed |
description | Correct orchestration of nervous system development is a profound challenge that involves coordination of complex molecular and cellular processes. Mechanistic target of rapamycin (mTOR) signaling is a key regulator of nervous system development and synaptic function. The mTOR kinase is a hub for sensing inputs including growth factor signaling, nutrients and energy levels. Activation of mTOR signaling causes diseases with severe neurological manifestations, such as tuberous sclerosis complex and focal cortical dysplasia. However, the molecular mechanisms by which mTOR signaling regulates nervous system development and function are poorly understood. Unkempt is a conserved zinc finger/RING domain protein that regulates neurogenesis downstream of mTOR signaling in Drosophila. Unkempt also directly interacts with the mTOR complex I component Raptor. Here we describe the generation and characterisation of mice with a conditional knockout of Unkempt (Unk(cKO)) in the nervous system. Loss of Unkempt reduces Raptor protein levels in the embryonic nervous system but does not affect downstream mTORC1 targets. We also show that nervous system development occurs normally in Unk(cKO) mice. However, we find that Unkempt is expressed in the adult cerebellum and hippocampus and behavioural analyses show that Unk(cKO) mice have improved memory formation and cognitive flexibility to re-learn. Further understanding of the role of Unkempt in the nervous system will provide novel mechanistic insight into the role of mTOR signaling in learning and memory. |
format | Online Article Text |
id | pubmed-8357790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83577902021-08-13 The zinc finger/RING domain protein Unkempt regulates cognitive flexibility Vinsland, Elin Baskaran, Pranetha Mihaylov, Simeon R. Hobbs, Carl Wood, Hannah Bouybayoune, Ihssane Shah, Kriti Houart, Corinne Tee, Andrew R. Murn, Jernej Fernandes, Cathy Bateman, Joseph M. Sci Rep Article Correct orchestration of nervous system development is a profound challenge that involves coordination of complex molecular and cellular processes. Mechanistic target of rapamycin (mTOR) signaling is a key regulator of nervous system development and synaptic function. The mTOR kinase is a hub for sensing inputs including growth factor signaling, nutrients and energy levels. Activation of mTOR signaling causes diseases with severe neurological manifestations, such as tuberous sclerosis complex and focal cortical dysplasia. However, the molecular mechanisms by which mTOR signaling regulates nervous system development and function are poorly understood. Unkempt is a conserved zinc finger/RING domain protein that regulates neurogenesis downstream of mTOR signaling in Drosophila. Unkempt also directly interacts with the mTOR complex I component Raptor. Here we describe the generation and characterisation of mice with a conditional knockout of Unkempt (Unk(cKO)) in the nervous system. Loss of Unkempt reduces Raptor protein levels in the embryonic nervous system but does not affect downstream mTORC1 targets. We also show that nervous system development occurs normally in Unk(cKO) mice. However, we find that Unkempt is expressed in the adult cerebellum and hippocampus and behavioural analyses show that Unk(cKO) mice have improved memory formation and cognitive flexibility to re-learn. Further understanding of the role of Unkempt in the nervous system will provide novel mechanistic insight into the role of mTOR signaling in learning and memory. Nature Publishing Group UK 2021-08-11 /pmc/articles/PMC8357790/ /pubmed/34381067 http://dx.doi.org/10.1038/s41598-021-95286-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Vinsland, Elin Baskaran, Pranetha Mihaylov, Simeon R. Hobbs, Carl Wood, Hannah Bouybayoune, Ihssane Shah, Kriti Houart, Corinne Tee, Andrew R. Murn, Jernej Fernandes, Cathy Bateman, Joseph M. The zinc finger/RING domain protein Unkempt regulates cognitive flexibility |
title | The zinc finger/RING domain protein Unkempt regulates cognitive flexibility |
title_full | The zinc finger/RING domain protein Unkempt regulates cognitive flexibility |
title_fullStr | The zinc finger/RING domain protein Unkempt regulates cognitive flexibility |
title_full_unstemmed | The zinc finger/RING domain protein Unkempt regulates cognitive flexibility |
title_short | The zinc finger/RING domain protein Unkempt regulates cognitive flexibility |
title_sort | zinc finger/ring domain protein unkempt regulates cognitive flexibility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8357790/ https://www.ncbi.nlm.nih.gov/pubmed/34381067 http://dx.doi.org/10.1038/s41598-021-95286-y |
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