Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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
_version_ 1783737210250461184
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
work_keys_str_mv AT vinslandelin thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT baskaranpranetha thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT mihaylovsimeonr thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT hobbscarl thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT woodhannah thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT bouybayouneihssane thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT shahkriti thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT houartcorinne thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT teeandrewr thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT murnjernej thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT fernandescathy thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT batemanjosephm thezincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT vinslandelin zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT baskaranpranetha zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT mihaylovsimeonr zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT hobbscarl zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT woodhannah zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT bouybayouneihssane zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT shahkriti zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT houartcorinne zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT teeandrewr zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT murnjernej zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT fernandescathy zincfingerringdomainproteinunkemptregulatescognitiveflexibility
AT batemanjosephm zincfingerringdomainproteinunkemptregulatescognitiveflexibility