|
|
|
|
JA Waddle, JA Cooper and RH Waterston
Department of Genetics, Washington University School of Medicine, St. Louis, Missouri 63110.
We cloned and analyzed two genes, cap-1 and cap-2, which encode the alpha and beta subunits of Caenorhabditis elegans capping protein (CP). The nematode CP subunits are 55% (cap-1) and 66% (cap-2) identical to the chicken CP subunits and 32% (cap-1) and 48% (cap-2) identical to the yeast CP subunits. Purified nematode CP made by expression of both subunits in yeast is functionally similar to chicken skeletal muscle CP in two different actin polymerization assays. The abnormal cell morphology and disorganized actin cytoskeleton of yeast CP null mutants are restored to wild-type by expression of the nematode CP subunits. Expression of the nematode CP alpha or beta subunit is sufficient to restore viability to yeast cap1 sac6 or cap2 sac6 double mutants, respectively. Therefore, despite evolution of the nematode actin cytoskeleton to a state far more complex than that of yeast, one important component can function in both organisms.
This article has been cited by other articles:
![]() |
K. Kim, A. Yamashita, M. A. Wear, Y. Maeda, and J. A. Cooper Capping protein binding to actin in yeast: biochemical mechanism and physiological relevance J. Cell Biol., February 16, 2004; 164(4): 567 - 580. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. C. Hart and J. A. Cooper Vertebrate Isoforms of Actin Capping Protein {beta} Have Distinct Functions In Vivo J. Cell Biol., December 13, 1999; 147(6): 1287 - 1298. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. A. Barron-Casella, M. A. Torres, S. W. Scherer, H. H. Q. Heng, L.-C. Tsui, and J. F. Casella Sequence Analysis and Chromosomal Localization of Human Cap Z J. Biol. Chem., September 15, 1995; 270(37): 21472 - 21479. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Waddle, J. Cooper, and R. Waterston Transient localized accumulation of actin in Caenorhabditis elegans blastomeres with oriented asymmetric divisions Development, January 8, 1994; 120(8): 2317 - 2328. [Abstract] [PDF] |
||||