Literature DB >> 26677825

Twist1 contributes to cranial bone initiation and dermal condensation by maintaining Wnt signaling responsiveness.

L Henry Goodnough1, Gregg J Dinuoscio2, Radhika P Atit2,3,4.   

Abstract

BACKGROUND: Specification of cranial bone and dermal fibroblast progenitors in the supraorbital arch mesenchyme is Wnt/β-catenin signaling-dependent. The mechanism underlying how these cells interpret instructive signaling cues and differentiate into these two lineages is unclear. Twist1 is a target of the Wnt/β-catenin signaling pathway and is expressed in cranial bone and dermal lineages.
RESULTS: Here, we show that onset of Twist1 expression in the mouse cranial mesenchyme is dependent on ectodermal Wnts and mesenchymal β-catenin activity. Conditional deletion of Twist1 in the supraorbital arch mesenchyme leads to cranial bone agenesis and hypoplastic dermis, as well as craniofacial malformation of eyes and palate. Twist1 is preferentially required for cranial bone lineage commitment by maintaining Wnt responsiveness. In the conditional absence of Twist1, the cranial dermis fails to condense and expand apically leading to extensive cranial dermal hypoplasia with few and undifferentiated hair follicles.
CONCLUSIONS: Thus, Twist1, a target of canonical Wnt/β-catenin signaling, also functions to maintain Wnt responsiveness and is a key effector for cranial bone fate selection and dermal condensation.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  craniofacial development; skin; skull bone

Mesh:

Substances:

Year:  2015        PMID: 26677825      PMCID: PMC4715624          DOI: 10.1002/dvdy.24367

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  59 in total

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2.  Requirement for Twist1 in frontonasal and skull vault development in the mouse embryo.

Authors:  Heidi Bildsoe; David A F Loebel; Vanessa J Jones; You-Tzung Chen; Richard R Behringer; Patrick P L Tam
Journal:  Dev Biol       Date:  2009-05-03       Impact factor: 3.582

3.  Cell lineage in mammalian craniofacial mesenchyme.

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Journal:  Mech Dev       Date:  2008-06-20       Impact factor: 1.882

Review 4.  Transcriptional control of skeletogenesis.

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5.  Deletion of mouse Porcn blocks Wnt ligand secretion and reveals an ectodermal etiology of human focal dermal hypoplasia/Goltz syndrome.

Authors:  Jared J Barrott; Gabriela M Cash; Aaron P Smith; Jeffery R Barrow; L Charles Murtaugh
Journal:  Proc Natl Acad Sci U S A       Date:  2011-07-18       Impact factor: 11.205

6.  Generation of mice with a conditional null allele for Wntless.

Authors:  April C Carpenter; Sujata Rao; James M Wells; Kenneth Campbell; Richard A Lang
Journal:  Genesis       Date:  2010-09       Impact factor: 2.487

Review 7.  Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literature.

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Journal:  Am J Med Genet A       Date:  2011-03-17       Impact factor: 2.802

8.  Ectodermal Wnt/β-catenin signaling shapes the mouse face.

Authors:  Bethany S Reid; Hui Yang; Vida Senkus Melvin; Makoto M Taketo; Trevor Williams
Journal:  Dev Biol       Date:  2010-11-16       Impact factor: 3.582

9.  Homozygous nonsense mutations in TWIST2 cause Setleis syndrome.

Authors:  Turgut Tukel; Drazen Šošić; Lihadh I Al-Gazali; Mónica Erazo; Jose Casasnovas; Hector L Franco; James A Richardson; Eric N Olson; Carmen L Cadilla; Robert J Desnick
Journal:  Am J Hum Genet       Date:  2010-08-13       Impact factor: 11.025

Review 10.  A twist of insight - the role of Twist-family bHLH factors in development.

Authors:  Ralston M Barnes; Anthony B Firulli
Journal:  Int J Dev Biol       Date:  2009       Impact factor: 2.203

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  11 in total

1.  Anti-osteogenic function of a LIM-homeodomain transcription factor LMX1B is essential to early patterning of the calvaria.

Authors:  Jeffry M Cesario; André Landin Malt; Jong Uk Chung; Michael P Khairallah; Krishnakali Dasgupta; Kesava Asam; Lindsay J Deacon; Veronica Choi; Asma A Almaidhan; Nadine A Darwiche; Jimin Kim; Randy L Johnson; Juhee Jeong
Journal:  Dev Biol       Date:  2018-05-28       Impact factor: 3.582

2.  Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura.

Authors:  Max A Tischfield; Caroline D Robson; Nicole M Gilette; Shek Man Chim; Folasade A Sofela; Michelle M DeLisle; Alon Gelber; Brenda J Barry; Sarah MacKinnon; Linda R Dagi; Jeremy Nathans; Elizabeth C Engle
Journal:  Dev Cell       Date:  2017-08-30       Impact factor: 12.270

3.  Tissue-specific analysis of Fgf18 gene function in palate development.

Authors:  Minghui Yue; Yu Lan; Han Liu; Zhaoming Wu; Toru Imamura; Rulang Jiang
Journal:  Dev Dyn       Date:  2020-10-21       Impact factor: 3.780

4.  Recombinant mouse periostin ameliorates coronal sutures fusion in Twist1+/- mice.

Authors:  Shanshan Bai; Dong Li; Liang Xu; Huichuan Duan; Jie Yuan; Min Wei
Journal:  J Transl Med       Date:  2018-04-17       Impact factor: 5.531

5.  PRC2 Is Dispensable in Vivo for β-Catenin-Mediated Repression of Chondrogenesis in the Mouse Embryonic Cranial Mesenchyme.

Authors:  James Ferguson; Mahima Devarajan; Gregg DiNuoscio; Alina Saiakhova; Chia-Feng Liu; Veronique Lefebvre; Peter C Scacheri; Radhika P Atit
Journal:  G3 (Bethesda)       Date:  2018-02-02       Impact factor: 3.154

6.  The FZD7-TWIST1 axis is responsible for anoikis resistance and tumorigenesis in ovarian carcinoma.

Authors:  Ming Tan; Mohammad Asad; Valerie Heong; Meng Kang Wong; Tuan Zea Tan; Jieru Ye; Kuee Theng Kuay; Jean Paul Thiery; Clare Scott; Ruby Yun-Ju Huang
Journal:  Mol Oncol       Date:  2019-01-19       Impact factor: 6.603

7.  Deregulation of Neuro-Developmental Genes and Primary Cilium Cytoskeleton Anomalies in iPSC Retinal Sheets from Human Syndromic Ciliopathies.

Authors:  Andrea Barabino; Anthony Flamier; Roy Hanna; Elise Héon; Benjamin S Freedman; Gilbert Bernier
Journal:  Stem Cell Reports       Date:  2020-03-10       Impact factor: 7.765

8.  Pharmacological targeting of KDM6A and KDM6B, as a novel therapeutic strategy for treating craniosynostosis in Saethre-Chotzen syndrome.

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Journal:  Stem Cell Res Ther       Date:  2020-12-09       Impact factor: 6.832

9.  FGF-induced LHX9 regulates the progression and metastasis of osteosarcoma via FRS2/TGF-β/β-catenin pathway.

Authors:  Shuang-Qing Li; Chao Tu; Lu Wan; Rui-Qi Chen; Zhi-Xi Duan; Xiao-Lei Ren; Zhi-Hong Li
Journal:  Cell Div       Date:  2019-11-25       Impact factor: 5.130

Review 10.  Cranial Neural Crest Cells and Their Role in the Pathogenesis of Craniofacial Anomalies and Coronal Craniosynostosis.

Authors:  Erica M Siismets; Nan E Hatch
Journal:  J Dev Biol       Date:  2020-09-09
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