Department of Cell and Developmental Biology, State University of NY Upstate Medical University, Syracuse, NY 13210, USA.
J Cell Biol. 2012 Jul 9;198(1):87-102. doi: 10.1083/jcb.201202053. Epub 2012 Jul 2.
Muscle contraction depends on interactions between actin and myosin filaments organized into sarcomeres, but the mechanism by which actin filaments incorporate into sarcomeres remains unclear. We have found that, during larval development in Caenorhabditis elegans, two members of the actin-assembling formin family, CYK-1 and FHOD-1, are present in striated body wall muscles near or on sarcomere Z lines, where barbed ends of actin filaments are anchored. Depletion of either formin during this period stunted growth of the striated contractile lattice, whereas their simultaneous reduction profoundly diminished lattice size and number of striations per muscle cell. CYK-1 persisted at Z lines in adulthood, and its near complete depletion from adults triggered phenotypes ranging from partial loss of Z line-associated filamentous actin to collapse of the contractile lattice. These results are, to our knowledge, the first genetic evidence implicating sarcomere-associated formins in the in vivo organization of the muscle cytoskeleton.
肌肉收缩依赖于肌动蛋白丝和肌球蛋白丝之间的相互作用,这些丝有序地组成肌节,但肌动蛋白丝如何整合到肌节中仍不清楚。我们发现,在秀丽隐杆线虫的幼虫发育过程中,两个肌动蛋白组装formin 家族成员,CYK-1 和 FHOD-1,存在于条纹体壁肌肉中,靠近或位于肌节 Z 线上,肌动蛋白丝的暴发性末端被锚定。在此期间,这两种formin 的耗尽都会阻碍条纹收缩晶格的生长,而它们的同时减少则会极大地减小晶格的大小和每个肌细胞的条纹数量。CYK-1 在成年后仍存在于 Z 线上,其在成年期的近乎完全耗尽会引发从 Z 线相关丝状肌动蛋白的部分缺失到收缩晶格崩溃的表型。据我们所知,这些结果是第一个遗传证据,表明肌节相关formin 参与了肌肉细胞骨架的体内组织。