A Mutation in the Amino-Terminal End of the Triple Helix of Type II Collagen Causing Severe Osteochondrodysplasia

Genomics ◽  
1993 ◽  
Vol 16 (1) ◽  
pp. 282-285 ◽  
Author(s):  
Miikka Vikkula ◽  
Pertti Ritvaniemi ◽  
Alpo F. Vuorio ◽  
Ilkka Kaitila ◽  
Leena Ala-Kokko ◽  
...  
Development ◽  
1992 ◽  
Vol 115 (1) ◽  
pp. 169-179
Author(s):  
R.E. Swiderski ◽  
M. Solursh

Using RNA blot analysis of developmentally staged avian limb buds, we demonstrate that transcripts of several cartilage marker genes appear in limb tissue prior to overt chondrogenesis. Type II collagen mRNA, cartilage proteoglycan core protein mRNA, alpha 2(IX) collagen mRNA, and transcripts of the short form alpha 1(IX) collagen chain derived from the downstream promoter are co-expressed in limb tissue approximately 24–36 hours before the appearance of the respective polypeptides in differentiating cartilagenous tissue. Transcripts of the long form alpha 1(IX) collagen chain derived from the upstream promoter appear somewhat later in development; nearly coincident with the immunolocalization of type IX collagen in the cartilage elements of the limb. The spatial distribution of type II and type IX collagen transcripts was analyzed by in situ hybridization. Type II collagen and the long form alpha 1(IX) collagen transcripts co-localized in the chondrogenic elements of the developing forelimb. In contrast, short form alpha 1(IX) collagen transcripts which lack the 5′ region encoding the NC4 globular amino-terminal domain were distributed throughout the non-chondrogenic, non-myogenic mesenchymal regions of the limb and were not detectable above background levels in the limb chondrogenic elements. The precocious appearance of several cartilage marker gene transcripts prior to chondrogenesis suggests that multiple levels of gene regulation including alternative promoter use, alternative RNA splicing, alternative polyadenylation, and other post-transcriptional as well as translational mechanisms are active prior to, and during avian limb chondrogenesis.


1998 ◽  
Vol 331 (3) ◽  
pp. 727-732 ◽  
Author(s):  
Wa'el KAFIENAH ◽  
Dieter BRÖMME ◽  
David J. BUTTLE ◽  
Lisa J. CROUCHER ◽  
Anthony P. HOLLANDER

Cathepsin K (EC 3.4.22.38) is a recently described enzyme that has been shown to cleave type I collagen in its triple helix. The aim of this study was to determine if it also cleaves type II collagen in the triple helix and to identify the helical cleavage site(s) in types I and II collagens. Soluble human and bovine type II collagen, and rat type I collagen, were incubated with cathepsin K before the reaction was stopped with trans-epoxysuccinyl-l-leucylamido-(4-guanidino)butane (E-64). Analysis by SDS/PAGE of the collagen digests showed that optimal activity of cathepsin K against native type II collagen was between pH 5.0 and 5.5 and against denatured collagen between pH 4.0 and 7.0. The enzyme cleaved telopeptides as well as the α1(II) chains, generating multiple fragments in the range 90–120 kDa. The collagenolytic activity was not due to a contaminating metalloenzyme or serine proteinase as it was not inhibited by 1,10-phenanthroline, EDTA or 3,4-dichloroisocoumarin. Western blotting with anti-peptide antibodies to different regions of the α1(II) chain suggested that cathepsin K cleaved native α1(II) chains in the N-terminal region of the helical domain rather than at the well-defined collagenase cleavage site. This was confirmed by N-terminal sequencing of one of the fragments, revealing cleavage at a Gly-Lys bond, 58 residues from the N-terminus of the helical domain. By using a similar approach, cathepsin K was found to cleave native type I collagen close to the N-terminus of its triple helix. These results indicate that cathepsin K could have a role in the turnover of type II collagen, as well as type I collagen.


2017 ◽  
Vol 5 (44) ◽  
pp. 8707-8718 ◽  
Author(s):  
Ke Yang ◽  
Jing Sun ◽  
Dan Wei ◽  
Lu Yuan ◽  
Jirong Yang ◽  
...  

Type II collagen methacrylamide with a triple helix was developed for 3D construction of a cartilaginous ECM-like microenvironment to induce chondrogenic differentiation of BMSCs.


1986 ◽  
Vol 237 (3) ◽  
pp. 923-925 ◽  
Author(s):  
M Van der Rest ◽  
L C Rosenberg ◽  
B R Olsen ◽  
A R Poole

The primary structure of the cartilage matrix molecule chondrocalcin has been found to be identical with that of the C-propeptide of type II procollagen by comparing sequence analyses of the N-terminal regions and of tryptic peptides derived from chondrocalcin. This implies that in type II collagen the C-propeptide of type II collagen is employed not only in the assembly of the triple helix of type II collagen, as demonstrated previously, but in calcifying cartilage it may also be involved in those events leading to cartilage calcification, as earlier indicated.


1994 ◽  
Vol 3 (11) ◽  
pp. 1999-2003 ◽  
Author(s):  
Douglas J.WIIkln ◽  
Ray Bogaert ◽  
Ralph S. Lachman ◽  
David L.Rimoin ◽  
David R. Eyre ◽  
...  

Author(s):  
Douglas J. Wilkin ◽  
Andrew S. Artz ◽  
Sarah South ◽  
Ralph S. Lachman ◽  
David L. Rimoin ◽  
...  

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