Literature DB >> 31586559

Yap/Taz are required for establishing the cerebellar radial glia scaffold and proper foliation.

Lucinda J Hughes1, Raehee Park2, Min Jung Lee2, Bethany K Terry1, David J Lee2, Hansol Kim2, Seo-Hee Cho2, Seonhee Kim3.   

Abstract

Yap/Taz are well-established downstream effectors of the Hippo pathway, known to regulate organ size by directing proliferation and apoptosis. Although the functions of Yap/Taz have been extensively studied, little is known about their role in brain development. Here, through genetic ablation, we show that Yap/Taz are required for cerebellar morphogenesis. Yap/Taz deletion in neural progenitors causes defects in secondary fissure formation, leading to abnormal folia development. Although they seemed very likely to serve an important function in the development of cerebellar granule cell precursors, Yap/Taz are dispensable for their proliferation. Furthermore, Yap/Taz loss does not rescue the medulloblastoma phenotype caused by constitutively active Smoothened. Importantly, Yap/Taz are highly expressed in radial glia and play a crucial role in establishing the radial scaffold and cellular polarity of neural progenitors during embryogenesis. We found that Yap/Taz are necessary to establish and maintain junctional integrity of cerebellar neuroepithelium as prominent junction proteins are not maintained at the apical junction in the absence of Yap/Taz. Our study identifies a novel function of Yap/Taz in cerebellar foliation and finds that they are required to establish the radial glia scaffold and junctional stability.
Copyright © 2019 Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 31586559      PMCID: PMC6910221          DOI: 10.1016/j.ydbio.2019.10.002

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  63 in total

1.  hGFAP-cre transgenic mice for manipulation of glial and neuronal function in vivo.

Authors:  L Zhuo; M Theis; I Alvarez-Maya; M Brenner; K Willecke; A Messing
Journal:  Genesis       Date:  2001-10       Impact factor: 2.487

2.  aPKC enables development of zonula adherens by antagonizing centripetal contraction of the circumferential actomyosin cables.

Authors:  Masaru Kishikawa; Atsushi Suzuki; Shigeo Ohno
Journal:  J Cell Sci       Date:  2008-07-15       Impact factor: 5.285

3.  YAP/TAZ regulates sprouting angiogenesis and vascular barrier maturation.

Authors:  Jongshin Kim; Yoo Hyung Kim; Jaeryung Kim; Do Young Park; Hosung Bae; Da-Hye Lee; Kyun Hoo Kim; Seon Pyo Hong; Seung Pil Jang; Yoshiaki Kubota; Young-Guen Kwon; Dae-Sik Lim; Gou Young Koh
Journal:  J Clin Invest       Date:  2017-08-14       Impact factor: 14.808

4.  Yes-associated protein 1 is widely expressed in human brain tumors and promotes glioblastoma growth.

Authors:  Brent A Orr; Haibo Bai; Yazmin Odia; Deepali Jain; Robert A Anders; Charles G Eberhart
Journal:  J Neuropathol Exp Neurol       Date:  2011-07       Impact factor: 3.685

5.  Hippo pathway effector Yap promotes cardiac regeneration.

Authors:  Mei Xin; Yuri Kim; Lillian B Sutherland; Masao Murakami; Xiaoxia Qi; John McAnally; Enzo R Porrello; Ahmed I Mahmoud; Wei Tan; John M Shelton; James A Richardson; Hesham A Sadek; Rhonda Bassel-Duby; Eric N Olson
Journal:  Proc Natl Acad Sci U S A       Date:  2013-08-05       Impact factor: 11.205

6.  Regulation of the Hippo-YAP pathway by G-protein-coupled receptor signaling.

Authors:  Fa-Xing Yu; Bin Zhao; Nattapon Panupinthu; Jenna L Jewell; Ian Lian; Lloyd H Wang; Jiagang Zhao; Haixin Yuan; Karen Tumaneng; Hairi Li; Xiang-Dong Fu; Gordon B Mills; Kun-Liang Guan
Journal:  Cell       Date:  2012-08-02       Impact factor: 41.582

Review 7.  Sticky situations: recent advances in control of cell adhesion during neuronal migration.

Authors:  David J Solecki
Journal:  Curr Opin Neurobiol       Date:  2012-05-02       Impact factor: 6.627

8.  YAP and TAZ control peripheral myelination and the expression of laminin receptors in Schwann cells.

Authors:  Yannick Poitelon; Camila Lopez-Anido; Kathleen Catignas; Caterina Berti; Marilena Palmisano; Courtney Williamson; Dominique Ameroso; Kansho Abiko; Yoonchan Hwang; Alex Gregorieff; Jeffrey L Wrana; Mohammadnabi Asmani; Ruogang Zhao; Fraser James Sim; Lawrence Wrabetz; John Svaren; Maria Laura Feltri
Journal:  Nat Neurosci       Date:  2016-06-06       Impact factor: 24.884

9.  Isolation and culture of post-natal mouse cerebellar granule neuron progenitor cells and neurons.

Authors:  Hae Young Lee; Lloyd A Greene; Carol A Mason; M Chiara Manzini
Journal:  J Vis Exp       Date:  2009-01-16       Impact factor: 1.355

10.  Cerebellum morphogenesis: the foliation pattern is orchestrated by multi-cellular anchoring centers.

Authors:  Anamaria Sudarov; Alexandra L Joyner
Journal:  Neural Dev       Date:  2007-12-03       Impact factor: 3.842

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  3 in total

1.  YAP/TAZ maintain the proliferative capacity and structural organization of radial glial cells during brain development.

Authors:  Alfonso Lavado; Ruchika Gangwar; Joshua Paré; Shibiao Wan; Yiping Fan; Xinwei Cao
Journal:  Dev Biol       Date:  2021-08-19       Impact factor: 3.582

2.  Abnormal activation of Yap/Taz contributes to the pathogenesis of tuberous sclerosis complex.

Authors:  Bethany K Terry; Raehee Park; Seo-Hee Cho; Peter B Crino; Seonhee Kim
Journal:  Hum Mol Genet       Date:  2022-06-22       Impact factor: 5.121

Review 3.  Human Cerebellar Development and Transcriptomics: Implications for Neurodevelopmental Disorders.

Authors:  Parthiv Haldipur; Kathleen J Millen; Kimberly A Aldinger
Journal:  Annu Rev Neurosci       Date:  2022-04-19       Impact factor: 15.553

  3 in total

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