Journal: J Biol Chem / Year: 2018 Title: Dystrophin's central domain forms a complex filament that becomes disorganized by in-frame deletions. Authors: Olivier Delalande / Anne-Elisabeth Molza / Raphael Dos Santos Morais / Angélique Chéron / Émeline Pollet / Céline Raguenes-Nicol / Christophe Tascon / Emmanuel Giudice / Marine Guilbaud ...Authors: Olivier Delalande / Anne-Elisabeth Molza / Raphael Dos Santos Morais / Angélique Chéron / Émeline Pollet / Céline Raguenes-Nicol / Christophe Tascon / Emmanuel Giudice / Marine Guilbaud / Aurélie Nicolas / Arnaud Bondon / France Leturcq / Nicolas Férey / Marc Baaden / Javier Perez / Pierre Roblin / France Piétri-Rouxel / Jean-François Hubert / Mirjam Czjzek / Elisabeth Le Rumeur / Abstract: Dystrophin, encoded by the gene, is critical for maintaining plasma membrane integrity during muscle contraction events. Mutations in the gene disrupting the reading frame prevent dystrophin ...Dystrophin, encoded by the gene, is critical for maintaining plasma membrane integrity during muscle contraction events. Mutations in the gene disrupting the reading frame prevent dystrophin production and result in severe Duchenne muscular dystrophy (DMD); in-frame internal deletions allow production of partly functional internally deleted dystrophin and result in less severe Becker muscular dystrophy (BMD). Many known BMD deletions occur in dystrophin's central domain, generally considered to be a monotonous rod-shaped domain based on the knowledge of spectrin family proteins. However, the effects caused by these deletions, ranging from asymptomatic to severe BMD, argue against the central domain serving only as a featureless scaffold. We undertook structural studies combining small-angle X-ray scattering and molecular modeling in an effort to uncover the structure of the central domain, as dystrophin has been refractory to characterization. We show that this domain appears to be a tortuous and complex filament that is profoundly disorganized by the most severe BMD deletion (loss of exons 45-47). Despite the preservation of large parts of the binding site for neuronal nitric oxide synthase (nNOS) in this deletion, computational approaches failed to recreate the association of dystrophin with nNOS. This observation is in agreement with a strong decrease of nNOS immunolocalization in muscle biopsies, a parameter related to the severity of BMD phenotypes. The structural description of the whole dystrophin central domain we present here is a first necessary step to improve the design of microdystrophin constructs toward the goal of a successful gene therapy for DMD.
Contact author
Elisabeth Le Rumeur (Université de Rennes 1, Institut Génétique et Développement de Rennes, France)
Instrument name: SOLEIL SWING / City: Saint-Aubin / 国: France / Type of source: X-ray synchrotron / Wavelength: 0.1 Å / Dist. spec. to detc.: 1.82 mm
Detector
Name: AVIEX / Type: CCD
Scan
Title: Human dystrophin central domain repeats 16 to 17 / Measurement date: Sep 19, 2012 / Storage temperature: 15 °C / Exposure time: 1.5 sec. / Number of frames: 20 / Unit: 1/nm /
Min
Max
Q
0.0625
6.0734
Distance distribution function P(R)
Sofotware P(R): GNOM 4.6 / Number of points: 271 /
Min
Max
Q
0.008806
0.315
P(R) point
5
275
R
0
128
Result
D max: 13 / Type of curve: single_conc /
Experimental
Porod
MW
29.4 kDa
29.4 kDa
Volume
-
47 nm3
P(R)
Guinier
Forward scattering, I0
0.065
0.0653
Radius of gyration, Rg
3.2 nm
3.11 nm
+
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Homo sapiens (human)
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