Literature DB >> 23869615

The expanded collagen VI family: new chains and new questions.

Jamie Fitzgerald1, Paul Holden, Uwe Hansen.   

Abstract

Collagen VI is a component of the extracellular matrix of almost all connective tissues, including cartilage, bone, tendon, muscles and cornea, where it forms abundant and structurally unique microfibrils organized into different suprastructural assemblies. The precise role of collagen VI is not clearly defined although it is most abundant in the interstitial matrix of tissues and often found in close association with basement membranes. Three genetically distinct collagen VI chains, α1(VI), α2(VI) and α3(VI), encoded by the COL6A1. COL6A2 and COL6A3 genes, were first described more than 20 years ago. Their molecular assembly and role in congenital muscular dystrophy has been broadly characterized. In 2008, three additional collagen VI genes arrayed in tandem at a single gene locus on chromosome 3q in humans, and chromosome 9 in mice, were described. Following the naming scheme for collagens the new genes were designated COL6A4. COL6A5 and COL6A6 encoding the α4(VI), α5(VI) and α6(VI) chains, respectively. This review will focus on the current state of knowledge of the three new chains.

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Year:  2013        PMID: 23869615      PMCID: PMC5248970          DOI: 10.3109/03008207.2013.822865

Source DB:  PubMed          Journal:  Connect Tissue Res        ISSN: 0300-8207            Impact factor:   3.417


  43 in total

1.  Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophy.

Authors:  Leona D Tooley; Laura K Zamurs; Nicola Beecher; Naomi L Baker; Rachel A Peat; Naomi E Adams; John F Bateman; Kathryn N North; Clair Baldock; Shireen R Lamandé
Journal:  J Biol Chem       Date:  2010-08-21       Impact factor: 5.157

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.  Amino acid sequence of the triple-helical domain of human collagen type VI.

Authors:  M L Chu; D Conway; T C Pan; C Baldwin; K Mann; R Deutzmann; R Timpl
Journal:  J Biol Chem       Date:  1988-12-15       Impact factor: 5.157

4.  Association of the DVWA and GDF5 polymorphisms with osteoarthritis in UK populations.

Authors:  A M Valdes; T D Spector; S Doherty; M Wheeler; D J Hart; M Doherty
Journal:  Ann Rheum Dis       Date:  2008-12-03       Impact factor: 19.103

5.  Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies.

Authors:  Matteo Bovolenta; Marcella Neri; Elena Martoni; Anna Urciuolo; Patrizia Sabatelli; Marina Fabris; Paolo Grumati; Eugenio Mercuri; Enrico Bertini; Luciano Merlini; Paolo Bonaldo; Alessandra Ferlini; Francesca Gualandi
Journal:  BMC Med Genet       Date:  2010-03-19       Impact factor: 2.103

Review 6.  Collagens.

Authors:  Marion K Gordon; Rita A Hahn
Journal:  Cell Tissue Res       Date:  2009-08-20       Impact factor: 5.249

7.  Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 loci.

Authors:  E Demir; A Ferreiro; P Sabatelli; V Allamand; S Makri; B Echenne; M Maraldi; L Merlini; H Topaloglu; P Guicheney
Journal:  Neuropediatrics       Date:  2004-04       Impact factor: 1.947

8.  Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis.

Authors:  Patrizia Sabatelli; Francesca Gualandi; Sudheer Kumar Gara; Paolo Grumati; Alessandra Zamparelli; Elena Martoni; Camilla Pellegrini; Luciano Merlini; Alessandra Ferlini; Paolo Bonaldo; Nadir Mario Maraldi; Mats Paulsson; Stefano Squarzoni; Raimund Wagener
Journal:  Matrix Biol       Date:  2011-12-30       Impact factor: 11.583

9.  Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis.

Authors:  Cilla Söderhäll; Ingo Marenholz; Tamara Kerscher; Franz Rüschendorf; Jorge Esparza-Gordillo; Margitta Worm; Christoph Gruber; Gabriele Mayr; Mario Albrecht; Klaus Rohde; Herbert Schulz; Ulrich Wahn; Norbert Hubner; Young-Ae Lee
Journal:  PLoS Biol       Date:  2007-09       Impact factor: 8.029

10.  Autosomal recessive myosclerosis myopathy is a collagen VI disorder.

Authors:  L Merlini; E Martoni; P Grumati; P Sabatelli; S Squarzoni; A Urciuolo; A Ferlini; F Gualandi; P Bonaldo
Journal:  Neurology       Date:  2008-10-14       Impact factor: 9.910

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  22 in total

1.  Transcriptome Sequencing Data Reveal LncRNA-miRNA-mRNA Regulatory Network in Calcified Aortic Valve Disease.

Authors:  Kai Huang; Lujia Wu; Yuan Gao; Qin Li; Hao Wu; Xiaohong Liu; Lin Han
Journal:  Front Cardiovasc Med       Date:  2022-05-26

2.  A collagen VI-dependent pathogenic mechanism for Hirschsprung's disease.

Authors:  Rodolphe Soret; Mathilde Mennetrey; Karl F Bergeron; Anne Dariel; Michel Neunlist; Franziska Grunder; Christophe Faure; David W Silversides; Nicolas Pilon
Journal:  J Clin Invest       Date:  2015-11-16       Impact factor: 14.808

3.  212th ENMC International Workshop: Animal models of congenital muscular dystrophies, Naarden, The Netherlands, 29-31 May 2015.

Authors:  M Saunier; C G Bönnemann; M Durbeej; V Allamand
Journal:  Neuromuscul Disord       Date:  2016-02-15       Impact factor: 4.296

4.  Co-culture of chondrons and mesenchymal stromal cells reduces the loss of collagen VI and improves extracellular matrix production.

Authors:  H A Owida; T De Las Heras Ruiz; A Dhillon; Y Yang; N J Kuiper
Journal:  Histochem Cell Biol       Date:  2017-08-19       Impact factor: 4.304

5.  Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families.

Authors:  Isaac Baldwin; Robin L Shafer; Waheeda A Hossain; Sumedha Gunewardena; Olivia J Veatch; Matthew W Mosconi; Merlin G Butler
Journal:  Int J Mol Sci       Date:  2021-02-07       Impact factor: 5.923

6.  Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies.

Authors:  F Tagliavini; C Pellegrini; F Sardone; S Squarzoni; M Paulsson; R Wagener; F Gualandi; C Trabanelli; A Ferlini; L Merlini; S Santi; N M Maraldi; C Faldini; P Sabatelli
Journal:  Biochim Biophys Acta       Date:  2014-06-05

7.  Immunogenicity of intensively decellularized equine carotid arteries is conferred by the extracellular matrix protein collagen type VI.

Authors:  Ulrike Boeer; Falk F R Buettner; Melanie Klingenberg; Georgios C Antonopoulos; Heiko Meyer; Axel Haverich; Mathias Wilhelmi
Journal:  PLoS One       Date:  2014-08-26       Impact factor: 3.240

8.  Splicing mutation analysis reveals previously unrecognized pathways in lymph node-invasive breast cancer.

Authors:  Stephanie N Dorman; Coby Viner; Peter K Rogan
Journal:  Sci Rep       Date:  2014-11-14       Impact factor: 4.379

9.  Maintenance and Acceleration of Pericellular Matrix Formation within 3D Cartilage Cell Culture Models.

Authors:  Hamza A Owida; Nicola L Kuiper; Ying Yang
Journal:  Cartilage       Date:  2019-08-28       Impact factor: 3.117

10.  New COL6A6 variant detected by whole-exome sequencing is linked to break points in intron 4 and 3'-UTR, deleting exon 5 of RHO, and causing adRP.

Authors:  Miguel de Sousa Dias; Imma Hernan; Barbara Delás; Beatriz Pascual; Emma Borràs; Maria José Gamundi; Begoña Mañé; Patricia Fernández-San José; Carmen Ayuso; Miguel Carballo
Journal:  Mol Vis       Date:  2015-08-18       Impact factor: 2.367

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