Literature DB >> 22174087

Hyperactive BMP signaling induced by ALK2(R206H) requires type II receptor function in a Drosophila model for classic fibrodysplasia ossificans progressiva.

Viet Q Le1, Kristi A Wharton.   

Abstract

BACKGROUND: Fibrodysplasia Ossificans Progressiva (FOP) is an autosomal dominant disorder characterized by episodic deposition of heterotopic bone in place of soft connective tissue. All FOP-associated mutations map to the BMP type I receptor, ALK2, with the ALK2(R206H) mutant form found in the vast majority of patients. The mechanism(s) regulating the expressivity of hyperactive ALK2(R206H) signaling throughout a patient's life is not well understood.
RESULTS: In Drosophila, human ALK2(R206H) receptor induces hyperactive BMP signaling. As in vertebrates, elevated signaling associated with ALK2(R206H) in Drosophila is ligand-independent. We found that a key determinant for ALK2(R206H) hyperactivity is a functional type II receptor. Furthermore, our results indicate that like its Drosophila ortholog, Saxophone (Sax), wild-type ALK2 can antagonize, as well as promote, BMP signaling.
CONCLUSIONS: The dual function of ALK2 is of particular interest given the heterozygous nature of FOP, as the normal interplay between such disparate behaviors could be shifted by the presence of ALK2(R206H) receptors. Our studies provide a compelling example for Drosophila as a model organism to study the molecular underpinnings of complex human syndromes such as FOP.
Copyright © 2011 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22174087      PMCID: PMC3454517          DOI: 10.1002/dvdy.22779

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


  100 in total

1.  The divergent TGF-beta ligand Dawdle utilizes an activin pathway to influence axon guidance in Drosophila.

Authors:  Louise Parker; Jeremy E Ellis; Minh Q Nguyen; Kavita Arora
Journal:  Development       Date:  2006-12       Impact factor: 6.868

2.  Dpp and Gbb exhibit different effective ranges in the establishment of the BMP activity gradient critical for Drosophila wing patterning.

Authors:  Erdem Bangi; Kristi Wharton
Journal:  Dev Biol       Date:  2006-04-27       Impact factor: 3.582

3.  Drosophila researchers focus on human disease.

Authors:  Juan Botas
Journal:  Nat Genet       Date:  2007-05       Impact factor: 38.330

4.  A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.

Authors:  Eileen M Shore; Meiqi Xu; George J Feldman; David A Fenstermacher; Tae-Joon Cho; In Ho Choi; J Michael Connor; Patricia Delai; David L Glaser; Martine LeMerrer; Rolf Morhart; John G Rogers; Roger Smith; James T Triffitt; J Andoni Urtizberea; Michael Zasloff; Matthew A Brown; Frederick S Kaplan
Journal:  Nat Genet       Date:  2006-04-23       Impact factor: 38.330

5.  Dual function of the Drosophila Alk1/Alk2 ortholog Saxophone shapes the Bmp activity gradient in the wing imaginal disc.

Authors:  Erdem Bangi; Kristi Wharton
Journal:  Development       Date:  2006-08-03       Impact factor: 6.868

6.  A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2.

Authors:  Katarina Lehmann; Petra Seemann; Jan Boergermann; Gilles Morin; Silke Reif; Petra Knaus; Stefan Mundlos
Journal:  Eur J Hum Genet       Date:  2006-09-06       Impact factor: 4.246

7.  Structure of the ternary signaling complex of a TGF-beta superfamily member.

Authors:  George P Allendorph; Wylie W Vale; Senyon Choe
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-03       Impact factor: 11.205

8.  Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations.

Authors:  L-E Wehner; B J Folz; L Argyriou; S Twelkemeyer; U Teske; U W Geisthoff; J A Werner; W Engel; K Nayernia
Journal:  Clin Genet       Date:  2006-03       Impact factor: 4.438

9.  Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: mutations and manifestations.

Authors:  Pinar Bayrak-Toydemir; Jamie McDonald; Boaz Markewitz; Susan Lewin; Franklin Miller; Lan-Szu Chou; Friederike Gedge; Wei Tang; Hillary Coon; Rong Mao
Journal:  Am J Med Genet A       Date:  2006-03-01       Impact factor: 2.802

Review 10.  Using FlyAtlas to identify better Drosophila melanogaster models of human disease.

Authors:  Venkateswara R Chintapalli; Jing Wang; Julian A T Dow
Journal:  Nat Genet       Date:  2007-06       Impact factor: 38.330

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  24 in total

Review 1.  Strategies for exploring TGF-β signaling in Drosophila.

Authors:  Aidan J Peterson; Michael B O'Connor
Journal:  Methods       Date:  2014-03-27       Impact factor: 3.608

Review 2.  Application of human induced pluripotent stem cells to model fibrodysplasia ossificans progressiva.

Authors:  Emilie Barruet; Edward C Hsiao
Journal:  Bone       Date:  2017-07-14       Impact factor: 4.398

3.  ACVR1 p.Q207E causes classic fibrodysplasia ossificans progressiva and is functionally distinct from the engineered constitutively active ACVR1 p.Q207D variant.

Authors:  Julia Haupt; Alexandra Deichsel; Katja Stange; Cindy Ast; Renata Bocciardi; Roberto Ravazzolo; Maja Di Rocco; Paola Ferrari; Antonio Landi; Frederick S Kaplan; Eileen M Shore; Carsten Reissner; Petra Seemann
Journal:  Hum Mol Genet       Date:  2014-05-22       Impact factor: 6.150

4.  Variant BMP receptor mutations causing fibrodysplasia ossificans progressiva (FOP) in humans show BMP ligand-independent receptor activation in zebrafish.

Authors:  Bettina E Mucha; Megumi Hashiguchi; Joseph Zinski; Eileen M Shore; Mary C Mullins
Journal:  Bone       Date:  2018-01-04       Impact factor: 4.398

5.  Neofunction of ACVR1 in fibrodysplasia ossificans progressiva.

Authors:  Kyosuke Hino; Makoto Ikeya; Kazuhiko Horigome; Yoshihisa Matsumoto; Hayao Ebise; Megumi Nishio; Kazuya Sekiguchi; Mitsuaki Shibata; Sanae Nagata; Shuichi Matsuda; Junya Toguchida
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-30       Impact factor: 11.205

6.  Alternative cleavage of the bone morphogenetic protein (BMP), Gbb, produces ligands with distinct developmental functions and receptor preferences.

Authors:  Edward N Anderson; Kristi A Wharton
Journal:  J Biol Chem       Date:  2017-09-18       Impact factor: 5.157

7.  Variable signaling activity by FOP ACVR1 mutations.

Authors:  Julia Haupt; Meiqi Xu; Eileen M Shore
Journal:  Bone       Date:  2017-10-31       Impact factor: 4.398

8.  Wisdom from the fly.

Authors:  Leila E Rieder; Erica N Larschan
Journal:  Trends Genet       Date:  2014-08-24       Impact factor: 11.639

9.  Cellular Hypoxia Promotes Heterotopic Ossification by Amplifying BMP Signaling.

Authors:  Haitao Wang; Carter Lindborg; Vitali Lounev; Jung-Hoon Kim; Ruth McCarrick-Walmsley; Meiqi Xu; Laura Mangiavini; Jay C Groppe; Eileen M Shore; Ernestina Schipani; Frederick S Kaplan; Robert J Pignolo
Journal:  J Bone Miner Res       Date:  2016-04-20       Impact factor: 6.741

Review 10.  Granting immunity to FOP and catching heterotopic ossification in the Act.

Authors:  Frederick S Kaplan; Robert J Pignolo; Eileen M Shore
Journal:  Semin Cell Dev Biol       Date:  2015-12-17       Impact factor: 7.727

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