Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation-Reference-Cited by-同舟云学术

Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation

Published:2018-06-05 Issue:17 Volume:27 Page:3060-3078
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Chatzifrangkeskou Maria¹,Yadin David²,Marais Thibaut¹,Chardonnet Solenne³,Cohen-Tannoudji Mathilde¹,Mougenot Nathalie⁴,Schmitt Alain⁵,Crasto Silvia⁶⁷,Di Pasquale Elisa⁶⁷,Macquart Coline¹,Tanguy Yannick¹,Jebeniani Imen⁸,Pucéat Michel⁸,Morales Rodriguez Blanca¹,Goldmann Wolfgang H⁹,Dal Ferro Matteo¹⁰,Biferi Maria-Grazia¹,Knaus Petra²,Bonne Gisèle¹,Worman Howard J¹¹¹²,Muchir Antoine¹

Affiliation:

1. Sorbonne Université, UPMC Paris 06, INSERM UMRS974, Center of Research in Myology, F-75013 Paris, France

2. Institute for Chemistry and Biochemistry, Freie Universität Berlin, 14195 Berlin, Germany

3. Sorbonne Université, UPMC Paris 06, INSERM, UMS29 Omique, F-75013 Paris, France

4. Sorbonne Université, UPMC Paris 06, INSERM, UMS28 Phénotypage du Petit Animal, Paris F-75013, France

5. Institut Cochin, INSERM U1016-CNRS UMR 8104, Université Paris Descartes-Sorbonne Paris Cité, Paris F-75014, France

6. Istituto Clinico Humanitas IRCCS, Milan, Italy

7. Istituto Ricerca Genetica e Biomedica, National Research Council of Italy, Milan 20089, Italy

8. Faculté de Médecine La Timone, Université Aix-Marseille, INSERM UMR910, Marseille 13005, France

9. Department of Physics, Friedrich-Alexander-University of Erlangen-Nuremberg, 91054 Erlangen, Germany

10. Cardiovascular Department, Ospedali Riuniti and University of Trieste, Trieste, Italy

11. Department of Medicine

12. Department of Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA

Funder

National Institutes of Health

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/27/17/3060/25505625/ddy215.pdf

Reference100 articles.

1. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy;Bonne;Nat. Genet,1999

2. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease;Fatkin;N. Engl. J. Med,1999

3. cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins (lamin sequence identity/divergent carboxyl terminal/a-helical domains/coiled coils/nuclear localization sequence);Fisher;Cell Biol,1986

4. Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins;McKeon;Nature,1986

5. Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C;Lin;J. Biol. Chem,1993

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