Bethlem myopathy and engineered collagen VI triple helical deletions prevent intracellular multimer assembly and protein secretion

Mutations in the genes that code for collagen VI subunits, COL6A1, COL6A2, and COL6A3, are the cause of the autosomal dominant disorder, Bethlem myopa thy, Although three different collagen VI structural mutations have previou sly been reported, the effect of these mutations on collagen VI assembly, s tructure, and function is currently unknown. We have characterized a new Be thlem myopathy mutation that results in skipping of COL6A1 exon 14 during p re-mRNA splicing and the deletion of 18 amino acids from the triple helical domain of the al(VI) chain. Sequencing of genomic DNA identified a G to A transition in the +1 position of the splice donor site of intron 14 in one allele, The mutant alpha 1(VI) chains associated intracellularly with alpha 2(VI) and alpha 3(VI) to form disulfide-bonded monomers, but further assem bly into dimers and tetramers was prevented, and molecules containing the m utant chain were not secreted. This triple helical deletion thus resulted i n production of half the normal amount of collagen VI, To further explore t he biosynthetic consequences of collagen VI triple helical deletions, an al pha 3(VI) cDNA expression construct containing a 202-amino acid deletion wi thin the triple helix was produced and stably expressed in SaOS-2 cells. Th e transfected mutant alpha(VI) chains associated with endogenous alpha 1(VI ) and alpha 2(VI) to form collagen VI monomers, but dimers and tetramers di d not form and the mutant-containing molecules were not secreted. Thus, del etions within the triple helical region of both the alpha 1(VI) and alpha 3 (VI) chains can prevent intracellular dimer and tetramer assembly and secre tion. These results provide the first evidence of the biosynthetic conseque nces of structural collagen VI mutations and suggest that functional protei n haploinsufficiency may be a common pathogenic mechanism in Bethlem myopat hy.