A Nebulin Ruler Does Not Dictate Thin Filament Lengths

被引:68
作者
Castillo, Angelica [2 ]
Nowak, Roberta [3 ]
Littlefield, Kimberly P. [1 ]
Fowler, Velia M. [3 ]
Littlefield, Ryan S. [1 ]
机构
[1] Univ Washington, Friday Harbor Labs, Ctr Cell Dynam, Friday Harbor, WA 98250 USA
[2] Chaminade Univ, Dept Forens Sci, Honolulu, HI USA
[3] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
关键词
SKELETAL-MUSCLE; POINTED ENDS; STRIATED-MUSCLE; GIANT PROTEINS; TROPOMODULIN; GENE; ULTRASTRUCTURE; IDENTIFICATION; MUTATIONS; SARCOMERE;
D O I
10.1016/j.bpj.2008.10.053
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To generate force, striated muscle requires overlap between uniform-length actin and myosin filaments. The hypothesis that a nebulin ruler mechanism specifies thin filament lengths by targeting where tropomodulin (Tmod) caps the slow-growing, pointed end has not been rigorously tested. Using fluorescent microscopy and quantitative image analysis, we found that nebulin extended 1.01-1.03 mu m from the Z-line, but Tmod localized 1.13-1.31 mu m from the Z-line, in seven different rabbit skeletal muscles. Because nebulin does not extend to the thin filament pointed ends, it can neither target Tmod capping nor specify thin filament lengths. We found instead a strong correspondence between thin filament lengths and titin isoform sizes for each muscle. Our results suggest the existence of a mechanism whereby nebulin specifies the minimum thin filament length and sarcomere length regulates and coordinates pointed-end dynamics to maintain the relative overlap of the thin and thick filaments during myofibril assembly.
引用
收藏
页码:1856 / 1865
页数:10
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