Literature DB >> 24801232

Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy.

Yan-Zhi Zhang1, Dan-Hua Zhao, Hai-Po Yang, Ai-Jie Liu, Xing-Zhi Chang, Dao-Jun Hong, Carsten Bonnemann, Yun Yuan, Xi-Ru Wu, Hui Xiong.   

Abstract

BACKGROUND: We determined the clinical and molecular genetic characteristics of 8 Chinese patients with Ullrich congenital muscular dystrophy (UCMD).
METHODS: Clinical data of probands were collected and muscle biopsies of patients were analyzed. Exons of COL6A1, COL6A2 and COL6A3 were analyzed by direct sequencing. Mutations in COL6A1, COL6A2 and COL6A3 were identified in 8 patients.
RESULTS: Among these mutations, 5 were novel [three in the triple helical domain (THD) and 2 in the second C-terminal (C2) domain]. We also identified five known missense or in-frame deletion mutations in THD and C domains. Immunohistochemical studies on muscle biopsies from patients showed reduced level of collagen VI at the muscle basement membrane and mis-localization of the protein in interstitial and perivascular regions.
CONCLUSIONS: The novel mutations we identified underscore the importance of THD and C2 domains in the assembly and function of collagen VI, thereby providing useful information for the genetic counseling of UCMD patients.

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Year:  2014        PMID: 24801232     DOI: 10.1007/s12519-014-0481-1

Source DB:  PubMed          Journal:  World J Pediatr            Impact factor:   2.764


  19 in total

Review 1.  Collagens and collagen-related diseases.

Authors:  J Myllyharju; K I Kivirikko
Journal:  Ann Med       Date:  2001-02       Impact factor: 4.709

2.  A comparative analysis of collagen VI production in muscle, skin and fibroblasts from 14 Ullrich congenital muscular dystrophy patients with dominant and recessive COL6A mutations.

Authors:  C Jimenez-Mallebrera; M A Maioli; J Kim; S C Brown; L Feng; A K Lampe; K Bushby; D Hicks; K M Flanigan; C Bonnemann; C A Sewry; F Muntoni
Journal:  Neuromuscul Disord       Date:  2006-08-28       Impact factor: 4.296

3.  Large genomic deletions: a novel cause of Ullrich congenital muscular dystrophy.

Authors:  A Reghan Foley; Ying Hu; Yaqun Zou; Michele Yang; Līvija Medne; Meganne Leach; Laura K Conlin; Nancy Spinner; Tamim H Shaikh; Marni Falk; Ann M Neumeyer; Laurie Bliss; Brian S Tseng; Thomas L Winder; Carsten G Bönnemann
Journal:  Ann Neurol       Date:  2011-01       Impact factor: 10.422

4.  Early onset collagen VI myopathies: Genetic and clinical correlations.

Authors:  Laura Briñas; Pascale Richard; Susana Quijano-Roy; Corine Gartioux; Céline Ledeuil; Emmanuelle Lacène; Samira Makri; Ana Ferreiro; Svetlana Maugenre; Haluk Topaloglu; Göknur Haliloglu; Isabelle Pénisson-Besnier; Pierre-Yves Jeannet; Luciano Merlini; Carmen Navarro; Annick Toutain; Denys Chaigne; Isabelle Desguerre; Christine de Die-Smulders; Murielle Dunand; Bernard Echenne; Bruno Eymard; Thierry Kuntzer; Kim Maincent; Michèle Mayer; Ghislaine Plessis; François Rivier; Filip Roelens; Tanya Stojkovic; Ana Lía Taratuto; Fabiana Lubieniecki; Soledad Monges; Christine Tranchant; Louis Viollet; Norma B Romero; Brigitte Estournet; Pascale Guicheney; Valérie Allamand
Journal:  Ann Neurol       Date:  2010-10       Impact factor: 10.422

5.  Natural history of Ullrich congenital muscular dystrophy.

Authors:  A Nadeau; M Kinali; M Main; C Jimenez-Mallebrera; A Aloysius; E Clement; B North; A Y Manzur; S A Robb; E Mercuri; F Muntoni
Journal:  Neurology       Date:  2009-07-07       Impact factor: 9.910

Review 6.  Collagen VI related muscle disorders.

Authors:  A K Lampe; K M D Bushby
Journal:  J Med Genet       Date:  2005-09       Impact factor: 6.318

7.  Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy.

Authors:  Naomi L Baker; Matthias Mörgelin; Rachel Peat; Nathalie Goemans; Kathryn N North; John F Bateman; Shireen R Lamandé
Journal:  Hum Mol Genet       Date:  2004-11-24       Impact factor: 6.150

8.  166th ENMC International Workshop on Collagen type VI-related Myopathies, 22-24 May 2009, Naarden, The Netherlands.

Authors:  Valérie Allamand; Luciano Merlini; Kate Bushby
Journal:  Neuromuscul Disord       Date:  2010-03-07       Impact factor: 4.296

9.  New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.

Authors:  Te-Cheng Pan; Rui-Zhu Zhang; Dominick G Sudano; Suely K Marie; Carsten G Bönnemann; Mon-Li Chu
Journal:  Am J Hum Genet       Date:  2003-07-01       Impact factor: 11.025

10.  Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan.

Authors:  M Okada; G Kawahara; S Noguchi; K Sugie; K Murayama; I Nonaka; Y K Hayashi; I Nishino
Journal:  Neurology       Date:  2007-09-04       Impact factor: 9.910

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  4 in total

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Authors:  Daniel D Lam; Rhîannan H Williams; Ernesto Lujan; Koji Tanabe; Georg Huber; Nay Lui Saw; Juliane Merl-Pham; Aaro V Salminen; David Lohse; Sally Spendiff; Melanie J Plastini; Michael Zech; Hanns Lochmüller; Arie Geerlof; Stefanie M Hauck; Mehrdad Shamloo; Marius Wernig; Juliane Winkelmann
Journal:  J Neurosci       Date:  2021-12-27       Impact factor: 6.709

2.  Aqueous Lumican Correlates with Central Retinal Thickness in Patients with Idiopathic Epiretinal Membrane: A Proteome Study.

Authors:  Wei-Cheng Chang; Cho-Hao Lee; Shih-Hwa Chiou; Chen-Chung Liao; Chao-Wen Cheng
Journal:  Dis Markers       Date:  2022-03-24       Impact factor: 3.464

3.  Use of RNA‑sequencing to detect abnormal transcription of the collagen α‑2 (VI) chain gene that can lead to Bethlem myopathy.

Authors:  Jingzi Zhong; Yanshu Xie; Yiwu Dang; Jiapeng Zhang; Yingru Song; Dan Lan
Journal:  Int J Mol Med       Date:  2021-02-04       Impact factor: 4.101

4.  "Target" and "Sandwich" Signs in Thigh Muscles have High Diagnostic Values for Collagen VI-related Myopathies.

Authors:  Jun Fu; Yi-Ming Zheng; Su-Qin Jin; Jun-Fei Yi; Xiu-Juan Liu; He Lyn; Zhao-Xia Wang; Wei Zhang; Jiang-Xi Xiao; Yun Yuan
Journal:  Chin Med J (Engl)       Date:  2016-08-05       Impact factor: 2.628

  4 in total

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