Alternative splicing of type II procollagen: IIB or not IIB?

被引:14
作者
McAlinden, Audrey [1 ]
机构
[1] Washington Univ, Sch Med, Musculoskeletal Res Ctr, Dept Orthopaed Surg, St Louis, MO 63130 USA
关键词
Alternative splicing; cartilage; chondrocyte differentiation; extracellular matrix; precursor mRNA; type II procollagen; type XI collagen; PRE-MESSENGER-RNA; RICH AMINO-PROPEPTIDE; XI COLLAGEN; DIFFERENTIAL EXPRESSION; STICKLER-SYNDROME; N-PROPEPTIDE; CARTILAGE; GENE; IDENTIFICATION; TISSUE;
D O I
10.3109/03008207.2014.908860
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Over two decades ago, two isoforms of the type II procollagen gene (COL2A1) were discovered. These isoforms, named IIA and IIB, are generated in a developmentally-regulated manner by alternative splicing of exon 2. Chondroprogenitor cells synthesize predominantly IIA isoforms (containing exon 2) while differentiated chondrocytes produce mainly IIB transcripts (devoid of exon 2). Importantly, this IIA-to-IIB alternative splicing switch occurs only during chondrogenesis. More recently, two other isoforms have been reported (IIC and IID) that also involve splicing of exon 2; these findings highlight the complexities involving regulation of COL2A1 expression. The biological significance of why different isoforms of COL2A1 exist within the context of skeletal development and maintenance is still not completely understood. This review will provide current knowledge on COL2A1 isoform expression during chondrocyte differentiation and what is known about some of the mechanisms that control exon 2 alternative splicing. Utilization of mouse models to address the biological significance of Col2a1 alternative splicing in vivo will also be discussed. From the knowledge acquired to date, some new questions and concepts are now being proposed on the importance of Col2a1 alternative splicing in regulating extracellular matrix assembly and how this may subsequently affect cartilage and endochondral bone quality and function.
引用
收藏
页码:165 / 176
页数:12
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