Abstract

BackgroundThe Hippo pathway regulates growth rate and organ size in fly and mouse, notably through control of cell proliferation. Molecular interactions at the heart of this pathway are known to have originated in the unicellular ancestry of metazoans. They notably involve a cascade of phosphorylations triggered by the kinase Hippo, with subsequent nuclear to cytoplasmic shift of Yorkie localisation, preventing its binding to the transcription factor Scalloped, thereby silencing proliferation genes. There are few comparative expression data of Hippo pathway genes in non-model animal species and notably none in non-bilaterian phyla.ResultsAll core Hippo pathway genes could be retrieved from the ctenophore Pleurobrachia pileus and the hydrozoan cnidarian Clytia hemisphaerica, with the important exception of Yorkie in ctenophore. Expression study of the Hippo, Salvador and Scalloped genes in tentacle “cellular conveyor belts” of these two organisms revealed striking differences. In P. pileus, their transcripts were detected in areas where undifferentiated progenitors intensely proliferate and where expression of cyclins B and D was also seen. In C. hemisphaerica, these three genes and Yorkie are expressed not only in the proliferating but also in the differentiation zone of the tentacle bulb and in mature tentacle cells. However, using an antibody designed against the C. hemiphaerica Yorkie protein, we show in two distinct cell lineages of the medusa that Yorkie localisation is predominantly nuclear in areas of active cell proliferation and mainly cytoplasmic elsewhere.ConclusionsThis is the first evidence of nucleocytoplasmic Yorkie shift in association with the arrest of cell proliferation in a cnidarian, strongly evoking the cell division-promoting role of this protein and its inhibition by the activated Hippo pathway in bilaterian models. Our results furthermore highlight important differences in terms of deployment and regulation of Hippo pathway genes between cnidarians and ctenophores.Electronic supplementary materialThe online version of this article (doi:10.1186/s13227-016-0041-y) contains supplementary material, which is available to authorized users.

Highlights

  • The Hippo pathway regulates growth rate and organ size in fly and mouse, notably through control of cell proliferation

  • This finding strengthens the hypothesis of an ancient role of Yki switches from the nucleus to the cytoplasm in the arrest of cell proliferation and initiation of differentiation

  • It would be desirable to describe the distribution of Yki in nuclei versus cytoplasm in other life stages of C. hemisphaerica using the anti-CheYki antibody designed in this study

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Summary

Introduction

The Hippo pathway regulates growth rate and organ size in fly and mouse, notably through control of cell proliferation. Yki is sequestered in the cytoplasm, notably through interaction with the 14-3-3 protein [26, 27] This prevents Yki from activating Sd in the nucleus ( down-regulating genes associated with stem cells and cell division), and it allows Yki to exert specific functions in the cytoplasm, including effects on cell fate and differentiation, documented in a number of systems [12, 28,29,30,31]. These core components of the Hippo pathway stand at the node of a complex network of interactions [5, 12]. There are Yki-independent effects of Hpo, as well as Hpo-independent regulations of Yki [12], further illustrating the complexity hiding behind what we call the “Hippo pathway”

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