Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Sci. Signal., 25 October 2011
Vol. 4, Issue 196, p. ra70
[DOI: 10.1126/scisignal.2002278]
RESEARCH ARTICLES
Editor's Summary
Growing a Heart
Understanding the signaling pathways that regulate heart growth during development provides possible avenues for regenerative therapies. In the fruit fly, the Hippo signaling pathway acts to limit organ size during development, and recent evidence indicates that this pathway also restricts cardiac growth in embryonic mice. Among other targets, activation of Hippo inhibits the transcriptional coactivator Yap. Mice generated by Xin et al. with a cardiomyocyte-specific deficiency of Yap developed smaller hearts and died in utero. In contrast, mice expressing a constitutively active form of Yap in the heart had larger hearts because of increased cell proliferation. In cardiomyocytes, expression of the constitutively active form of Yap increased the activity of the insulin-like growth factor (IGF) pathway, which resulted in stabilization of β-catenin, a transcriptional effector of the Wnt signaling pathway that promotes cardiomyocyte proliferation. Thus, alleviating the Hippo pathway–mediated inhibition of Yap increases the activity of signaling pathways that increase the growth of the heart during development.
Citation: M. Xin, Y. Kim, L. B. Sutherland, X. Qi, J. McAnally, R. J. Schwartz, J. A. Richardson, R. Bassel-Duby, E. N. Olson, Regulation of Insulin-Like Growth Factor Signaling by Yap Governs Cardiomyocyte Proliferation and Embryonic Heart Size. Sci. Signal.4, ra70 (2011).
The editors suggest the following Related Resources on Science sites:
In Science Signaling
EDITORS' CHOICE
Annalisa M. VanHook (12 February 2013) Sci. Signal.6 (262), ec38.
[DOI: 10.1126/scisignal.2004053] |Abstract »
EDITORS' CHOICE
John F. Foley (8 January 2013) Sci. Signal.6 (257), ec6.
[DOI: 10.1126/scisignal.2003940] |Abstract »
EDITORS' CHOICE
Wei Wong (11 December 2012) Sci. Signal.5 (254), ec318.
[DOI: 10.1126/scisignal.2003857] |Abstract »
EDITORS' CHOICE
Annalisa M. VanHook (18 September 2012) Sci. Signal.5 (242), ec245.
[DOI: 10.1126/scisignal.2003613] |Abstract »
EDITORS' CHOICE
John F. Foley (21 August 2012) Sci. Signal.5 (238), ec218.
[DOI: 10.1126/scisignal.2003518] |Abstract »
PODCASTS
Douglas J. Emlen and Annalisa M. VanHook (14 August 2012) Sci. Signal.5 (237), pc19.
[DOI: 10.1126/scisignal.2003437] |Abstract »|Full Text »|Podcast »
EDITORS' CHOICE
Annalisa M. VanHook (13 March 2012) Sci. Signal.5 (215), ec80.
[DOI: 10.1126/scisignal.2003032] |Abstract »
EDITORS' CHOICE
Paula A. Kiberstis (1 November 2011) Sci. Signal.4 (197), ec307.
[DOI: 10.1126/scisignal.4197ec307] |Abstract »
PERSPECTIVES
Elsa R. Flores and Georg Halder (26 July 2011) Sci. Signal.4 (183), pe34.
[DOI: 10.1126/scisignal.2002311] |Abstract »|Full Text »|PDF »
RESEARCH ARTICLES
Mark R. Silvis, Bridget T. Kreger, Wen-Hui Lien, Olga Klezovitch, G. Marianna Rudakova, Fernando D. Camargo, Dan M. Lantz, John T. Seykora, and Valeri Vasioukhin (24 May 2011) Sci. Signal.4 (174), ra33.
[DOI: 10.1126/scisignal.2001823] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
Yes-associated Protein Isoform 1 (Yap1) Promotes Cardiomyocyte Survival and Growth to Protect against Myocardial Ischemic Injury.
D. P. Del Re, Y. Yang, N. Nakano, J. Cho, P. Zhai, T. Yamamoto, N. Zhang, N. Yabuta, H. Nojima, D. Pan, et al. (2013)
J. Biol. Chem.
288, 3977-3988
|Abstract »|Full Text »|PDF »
Intersection of Hippo/YAP and Wnt/{beta}-catenin signaling pathways.
W. M. Konsavage Jr and G. S. Yochum (2013)
Acta Biochim Biophys Sin
45, 71-79
|Abstract »|Full Text »|PDF »
In vivo monitoring of cardiomyocyte proliferation to identify chemical modifiers of heart regeneration.
W.-Y. Choi, M. Gemberling, J. Wang, J. E. Holdway, M.-C. Shen, R. O. Karlstrom, and K. D. Poss (2013)
Development
140, 660-666
|Abstract »|Full Text »|PDF »
FoxO1 and FoxM1 Transcription Factors Have Antagonistic Functions in Neonatal Cardiomyocyte Cell-Cycle Withdrawal and IGF1 Gene Regulation.
A. Sengupta, V. V. Kalinichenko, and K. E. Yutzey (2013)
Circ. Res.
112, 267-277
|Abstract »|Full Text »|PDF »
14-3-3{varepsilon} Plays a Role in Cardiac Ventricular Compaction by Regulating the Cardiomyocyte Cell Cycle.
Y. Kosaka, K. A. Cieslik, L. Li, G. Lezin, C. T. Maguire, Y. Saijoh, K. Toyo-oka, M. J. Gambello, M. Vatta, A. Wynshaw-Boris, et al. (2012)
Mol. Cell. Biol.
32, 5089-5102
|Abstract »|Full Text »|PDF »
Yap1 Protein Regulates Vascular Smooth Muscle Cell Phenotypic Switch by Interaction with Myocardin.
C. Xie, Y. Guo, T. Zhu, J. Zhang, P. X. Ma, and Y. E. Chen (2012)
J. Biol. Chem.
287, 14598-14605
|Abstract »|Full Text »|PDF »