Hippo signaling instructs ectopic but not normal organ growth

Author:

Kowalczyk W.1ORCID,Romanelli L.1ORCID,Atkins M.12ORCID,Hillen H.1ORCID,Bravo González-Blas C.3ORCID,Jacobs J.3ORCID,Xie J.1ORCID,Soheily S.1ORCID,Verboven E.1ORCID,Moya I. M.14ORCID,Verhulst S.5ORCID,de Waegeneer M.3ORCID,Sansores-Garcia L.1ORCID,van Huffel L.1,Johnson R. L.6ORCID,van Grunsven L. A.5ORCID,Aerts S.3ORCID,Halder G.1ORCID

Affiliation:

1. VIB Center for Cancer Biology and KU Leuven Department of Oncology, KU Leuven, Leuven, Belgium.

2. Department of Biological Sciences, Sam Houston State University, Huntsville, TX, USA.

3. VIB Center for Brain and Disease Research and KU Leuven Department of Neurosciences, KU Leuven, Leuven, Belgium.

4. Facultad de Ingeniería y Ciencias Aplicadas, Universidad de Las Américas, Quito, Ecuador.

5. Department for Cell Biology, Faculty of Medicine and Pharmacy, Vrije Universiteit Brussel, Brussel-Jette, Belgium.

6. The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Abstract

The Hippo signaling pathway is widely considered a master regulator of organ growth because of the prominent overgrowth phenotypes caused by experimental manipulation of its activity. Contrary to this model, we show here that removing Hippo transcriptional output did not impair the ability of the mouse liver and Drosophila eyes to grow to their normal size. Moreover, the transcriptional activity of the Hippo pathway effectors Yap/Taz/Yki did not correlate with cell proliferation, and hyperactivation of these effectors induced gene expression programs that did not recapitulate normal development. Concordantly, a functional screen in Drosophila identified several Hippo pathway target genes that were required for ectopic overgrowth but not normal growth. Thus, Hippo signaling does not instruct normal growth, and the Hippo-induced overgrowth phenotypes are caused by the activation of abnormal genetic programs.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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