Hakeda S, Endo S, Saigo K
Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan.
J Cell Biol. 2000 Jan 10;148(1):101-14. doi: 10.1083/jcb.148.1.101.
Kettin is a giant muscle protein originally identified in insect flight muscle Z-discs. Here, we determined the entire nucleotide sequence of Drosophila melanogaster kettin, deduced the amino acid sequence of its protein product (540 kD) along with that of the Caenorhabditis elegans counterpart, and found that the overall primary structure of Kettin has been highly conserved in evolution. The main body of Drosophila Kettin consists of 35 immunoglobulin C2 domains separated by spacers. The central two thirds of spacers are constant in length and share in common two conserved motifs, putative actin binding sites. Neither fibronectin type III nor kinase domains were found. Kettin is present at the Z-disc in several muscle types. Genetic analysis showed that kettin is essential for the formation and maintenance of normal sarcomere structure of muscles and muscle tendons. Accordingly, embryos lacking kettin activity cannot hatch nor can adult flies heterozygous for the kettin mutation fly.
结蛋白是一种巨大的肌肉蛋白,最初在昆虫飞行肌的Z线中被鉴定出来。在此,我们测定了黑腹果蝇结蛋白的完整核苷酸序列,推导了其蛋白质产物(540 kD)以及秀丽隐杆线虫对应物的氨基酸序列,发现结蛋白的整体一级结构在进化过程中高度保守。果蝇结蛋白的主体由35个免疫球蛋白C2结构域组成,中间由间隔区隔开。间隔区的中间三分之二长度恒定,共有两个保守基序,即假定的肌动蛋白结合位点。未发现纤连蛋白III型结构域和激酶结构域。结蛋白存在于多种肌肉类型的Z线处。遗传分析表明,结蛋白对于肌肉和肌腱正常肌节结构的形成和维持至关重要。因此,缺乏结蛋白活性的胚胎无法孵化,结蛋白突变杂合的成年果蝇也无法飞行。