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Citron kinase interacts with LATS2 and inhibits its activity by occluding its hydrophobic phosphorylation motif

The inhibitory effect of large tumor suppressor kinase (LATS1/2) on the activity of the oncoprotein yes-associated protein (YAP) is crucial to maintain tissue homeostasis. Proteomic studies have identified several new regulators of this process. Recently, citron kinase (CIT) was listed as a potentia...

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Autores principales: Tran, Thi Hai Yen, Yang, Dae-Wook, Kim, Minchul, Lee, Da-Hye, Gai, Marta, Di Cunto, Ferdinando, Choi, Kwang-Wook, Lim, Dae-Sik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927243/
https://www.ncbi.nlm.nih.gov/pubmed/30865227
http://dx.doi.org/10.1093/jmcb/mjz013
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author Tran, Thi Hai Yen
Yang, Dae-Wook
Kim, Minchul
Lee, Da-Hye
Gai, Marta
Di Cunto, Ferdinando
Choi, Kwang-Wook
Lim, Dae-Sik
author_facet Tran, Thi Hai Yen
Yang, Dae-Wook
Kim, Minchul
Lee, Da-Hye
Gai, Marta
Di Cunto, Ferdinando
Choi, Kwang-Wook
Lim, Dae-Sik
author_sort Tran, Thi Hai Yen
collection PubMed
description The inhibitory effect of large tumor suppressor kinase (LATS1/2) on the activity of the oncoprotein yes-associated protein (YAP) is crucial to maintain tissue homeostasis. Proteomic studies have identified several new regulators of this process. Recently, citron kinase (CIT) was listed as a potential binding candidate of Hippo-related components, suggesting a new connection between CIT and the Hippo pathway. Aside from CIT’s role in cytokinesis, the molecular crosstalk between CIT and the Hippo pathway is largely unknown. Here, we demonstrate a role for CIT as a scaffold protein linking LATS2 and YAP. More importantly, CIT interacts with LATS2 to directly suppress LATS2 phosphorylation at the hydrophobic motif—targeted by MST1, leading to LATS2 inactivation and YAP activation. By studying their genetic interactions, we found that Sticky, the CIT homolog in Drosophila melanogaster, functions with Warts to control Drosophila eye development. Together, our study confirms citron kinase as a novel regulator of the Hippo pathway.
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spelling pubmed-69272432019-12-27 Citron kinase interacts with LATS2 and inhibits its activity by occluding its hydrophobic phosphorylation motif Tran, Thi Hai Yen Yang, Dae-Wook Kim, Minchul Lee, Da-Hye Gai, Marta Di Cunto, Ferdinando Choi, Kwang-Wook Lim, Dae-Sik J Mol Cell Biol Original Article The inhibitory effect of large tumor suppressor kinase (LATS1/2) on the activity of the oncoprotein yes-associated protein (YAP) is crucial to maintain tissue homeostasis. Proteomic studies have identified several new regulators of this process. Recently, citron kinase (CIT) was listed as a potential binding candidate of Hippo-related components, suggesting a new connection between CIT and the Hippo pathway. Aside from CIT’s role in cytokinesis, the molecular crosstalk between CIT and the Hippo pathway is largely unknown. Here, we demonstrate a role for CIT as a scaffold protein linking LATS2 and YAP. More importantly, CIT interacts with LATS2 to directly suppress LATS2 phosphorylation at the hydrophobic motif—targeted by MST1, leading to LATS2 inactivation and YAP activation. By studying their genetic interactions, we found that Sticky, the CIT homolog in Drosophila melanogaster, functions with Warts to control Drosophila eye development. Together, our study confirms citron kinase as a novel regulator of the Hippo pathway. Oxford University Press 2019-03-13 /pmc/articles/PMC6927243/ /pubmed/30865227 http://dx.doi.org/10.1093/jmcb/mjz013 Text en © The Author(s) (2019). Published by Oxford University Press on behalf of Journal of Molecular Cell Biology, IBCB, SIBS, CAS. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Tran, Thi Hai Yen
Yang, Dae-Wook
Kim, Minchul
Lee, Da-Hye
Gai, Marta
Di Cunto, Ferdinando
Choi, Kwang-Wook
Lim, Dae-Sik
Citron kinase interacts with LATS2 and inhibits its activity by occluding its hydrophobic phosphorylation motif
title Citron kinase interacts with LATS2 and inhibits its activity by occluding its hydrophobic phosphorylation motif
title_full Citron kinase interacts with LATS2 and inhibits its activity by occluding its hydrophobic phosphorylation motif
title_fullStr Citron kinase interacts with LATS2 and inhibits its activity by occluding its hydrophobic phosphorylation motif
title_full_unstemmed Citron kinase interacts with LATS2 and inhibits its activity by occluding its hydrophobic phosphorylation motif
title_short Citron kinase interacts with LATS2 and inhibits its activity by occluding its hydrophobic phosphorylation motif
title_sort citron kinase interacts with lats2 and inhibits its activity by occluding its hydrophobic phosphorylation motif
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927243/
https://www.ncbi.nlm.nih.gov/pubmed/30865227
http://dx.doi.org/10.1093/jmcb/mjz013
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