Invertebrate connectin spans as much as 3.5 μm in the giant sarcomeres of crayfish claw muscle

被引:29
作者
Fukuzawa, A
Shimamura, J
Takemori, S
Kanzawa, N
Yamaguchi, M
Sun, P
Maruyama, K
Kimura, S [1 ]
机构
[1] Chiba Univ, Fac Sci, Dept Biol, Chiba 2638522, Japan
[2] Jikei Univ, Sch Med, Dept Physiol, Tokyo 1058461, Japan
[3] Sophia Univ, Fac Sci & Technol, Dept Chem, Tokyo 1028554, Japan
[4] Natl Ctr Univ Entrance Examinat, Tokyo 1538501, Japan
关键词
connectin; D-titin; elasticity; kettin; titin;
D O I
10.1093/emboj/20.17.4826
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In crayfish claw closer muscle, the giant sarcomeres are 8.3 mum long at rest, four times longer than vertebrate striated muscle sarcomeres, and they are extensible up to 13 mum upon stretch. Invertebrate connectin (I-connectin) is an elastic protein which holds the A band at the center of the sarcomere. The entire sequence of crayfish I-connectin was predicted from cDNA sequences of 53 424 bp (17 352 residues; 1960 kDa). Crayfish I-connectin contains two novel 68- and 71-residue repeats, and also two PEVK domains and one kettin region. Kettin is a small isoform of I-connectin. Immunoblot tests using antibody to the 68-residue repeats revealed the presence of I-connectin also in long sarcomeres of insect leg muscle and barnacle ventral muscle. Immunofluorescence microscopy demonstrated that the two repeats, the long spacer and the two PEVK domains contribute to sarcomere extension. These regions rich in charged amino acids, occupying 63% of the crayfish I-connectin molecule, may allow a span of a 3.5 mum distance as a new class of composite spring.
引用
收藏
页码:4826 / 4835
页数:10
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