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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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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. |
format | Online Article Text |
id | pubmed-6927243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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