Premetazoan Origin of the Hippo Signaling Pathway

Nonaggregative multicellularity requires strict control of cell number. The Hippo signaling pathway coordinates cell proliferation and apoptosis and is a central regulator of organ size in animals. Recent studies have shown the presence of key members of the Hippo pathway in nonbilaterian animals, but failed to identify this pathway outside Metazoa. Through comparative analyses of recently sequenced holozoan genomes, we show that Hippo pathway components, such as the kinases Hippo and Warts, the coactivator Yorkie, and the transcription factor Scalloped, were already present in the unicellular ancestors of animals. Remarkably, functional analysis of Hippo components of the amoeboid holozoan Capsaspora owczarzaki, performed in Drosophila melanogaster, demonstrate that the growth-regulatory activity of the Hippo pathway is conserved in this unicellular lineage. Our findings show that the Hippo pathway evolved well before the origin of Metazoa and highlight the importance of Hippo signaling as a key developmental mechanism predating the origin of Metazoa. © 2012 The Authors.

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Main Authors: Sebé-Pedrós, Arnau, Zheng, Yonggang, Ruiz-Trillo, Iñaki, Pan, Duojia
Other Authors: European Research Council
Format: artículo biblioteca
Published: Elsevier 2012-01-26
Online Access:http://hdl.handle.net/10261/115532
http://dx.doi.org/10.13039/501100000781
http://dx.doi.org/10.13039/501100002809
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/100000002
http://dx.doi.org/10.13039/100000011
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spelling dig-ibe-es-10261-1155322021-12-27T15:34:21Z Premetazoan Origin of the Hippo Signaling Pathway Sebé-Pedrós, Arnau Zheng, Yonggang Ruiz-Trillo, Iñaki Pan, Duojia European Research Council Generalitat de Catalunya Ministerio de Ciencia e Innovación (España) National Institutes of Health (US) Howard Hughes Medical Institute Nonaggregative multicellularity requires strict control of cell number. The Hippo signaling pathway coordinates cell proliferation and apoptosis and is a central regulator of organ size in animals. Recent studies have shown the presence of key members of the Hippo pathway in nonbilaterian animals, but failed to identify this pathway outside Metazoa. Through comparative analyses of recently sequenced holozoan genomes, we show that Hippo pathway components, such as the kinases Hippo and Warts, the coactivator Yorkie, and the transcription factor Scalloped, were already present in the unicellular ancestors of animals. Remarkably, functional analysis of Hippo components of the amoeboid holozoan Capsaspora owczarzaki, performed in Drosophila melanogaster, demonstrate that the growth-regulatory activity of the Hippo pathway is conserved in this unicellular lineage. Our findings show that the Hippo pathway evolved well before the origin of Metazoa and highlight the importance of Hippo signaling as a key developmental mechanism predating the origin of Metazoa. © 2012 The Authors. This work was supported by an Institució Catalana per a la Recerca i Estudis Avançats contract, a European Research Council Starting Grant (ERC-2007-StG-206883), a grant (BFU2008-02839/BMC) from Ministerio de Ciencia e Innovación (MICINN) to I. R.-T., and a National Institutes of Health grant (R01 EY015708) to D.P. A.S-P. was supported by a pregraduate Formacion Profesorado Universitario grant from MICINN. D.P. is an investigator of the Howard Hughes Medical Institute. Peer Reviewed 2015-05-21T07:44:21Z 2015-05-21T07:44:21Z 2012-01-26 2015-05-21T07:44:22Z artículo http://purl.org/coar/resource_type/c_6501 doi: 10.1016/j.celrep.2011.11.004 issn: 2211-1247 Cell Reports 1(1): 13-20 (2012) http://hdl.handle.net/10261/115532 10.1016/j.celrep.2011.11.004 http://dx.doi.org/10.13039/501100000781 http://dx.doi.org/10.13039/501100002809 http://dx.doi.org/10.13039/501100004837 http://dx.doi.org/10.13039/100000002 http://dx.doi.org/10.13039/100000011 22832104 Publisher's version http://dx.doi.org/10.1016/j.celrep.2011.11.004 Sí open Elsevier
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country España
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libraryname Biblioteca del IBE España
description Nonaggregative multicellularity requires strict control of cell number. The Hippo signaling pathway coordinates cell proliferation and apoptosis and is a central regulator of organ size in animals. Recent studies have shown the presence of key members of the Hippo pathway in nonbilaterian animals, but failed to identify this pathway outside Metazoa. Through comparative analyses of recently sequenced holozoan genomes, we show that Hippo pathway components, such as the kinases Hippo and Warts, the coactivator Yorkie, and the transcription factor Scalloped, were already present in the unicellular ancestors of animals. Remarkably, functional analysis of Hippo components of the amoeboid holozoan Capsaspora owczarzaki, performed in Drosophila melanogaster, demonstrate that the growth-regulatory activity of the Hippo pathway is conserved in this unicellular lineage. Our findings show that the Hippo pathway evolved well before the origin of Metazoa and highlight the importance of Hippo signaling as a key developmental mechanism predating the origin of Metazoa. © 2012 The Authors.
author2 European Research Council
author_facet European Research Council
Sebé-Pedrós, Arnau
Zheng, Yonggang
Ruiz-Trillo, Iñaki
Pan, Duojia
format artículo
author Sebé-Pedrós, Arnau
Zheng, Yonggang
Ruiz-Trillo, Iñaki
Pan, Duojia
spellingShingle Sebé-Pedrós, Arnau
Zheng, Yonggang
Ruiz-Trillo, Iñaki
Pan, Duojia
Premetazoan Origin of the Hippo Signaling Pathway
author_sort Sebé-Pedrós, Arnau
title Premetazoan Origin of the Hippo Signaling Pathway
title_short Premetazoan Origin of the Hippo Signaling Pathway
title_full Premetazoan Origin of the Hippo Signaling Pathway
title_fullStr Premetazoan Origin of the Hippo Signaling Pathway
title_full_unstemmed Premetazoan Origin of the Hippo Signaling Pathway
title_sort premetazoan origin of the hippo signaling pathway
publisher Elsevier
publishDate 2012-01-26
url http://hdl.handle.net/10261/115532
http://dx.doi.org/10.13039/501100000781
http://dx.doi.org/10.13039/501100002809
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/100000002
http://dx.doi.org/10.13039/100000011
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