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2006 Abstracts - American Society of Animal Science

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59 Interactions <strong>of</strong> a novel intermediate filament protein withtwo costameric proteins in muscle cells. N. Sun* and R. M. Robson,Iowa State University, Ames.The novel intermediate filament (IF) protein synemin and the major IFprotein desmin comprise the heteropolymeric intermediate filaments(IFs) that surround the my<strong>of</strong>ibrillar Z-lines and link all adjacent my<strong>of</strong>ibrilswithin striated muscle cells. In addition, the heteropolymeric IFslink Z-lines <strong>of</strong> the peripheral layer <strong>of</strong> cellular my<strong>of</strong>ibrils to costamereslocated periodically along, and immediately subjacent to, the sarcolemma.In mammalian muscle cells, synemin is expressed as a larger Α-synemin splice variant, and a smaller Β splice variant. This differs fromavian muscle cells that express only one is<strong>of</strong>orm, an ortholog <strong>of</strong> mammalianΑ-synemin. Avian synemin has previously been shown in our labto interact with vinculin. The detailed functions <strong>of</strong> the two syneminis<strong>of</strong>orms in mammalian muscle cells have remained unclear. The objective<strong>of</strong> this study was to determine whether one or both <strong>of</strong> the mammalianis<strong>of</strong>orms <strong>of</strong> synemin interacts with the costameric proteins vinculinand/or talin. Herein we report specific interactions <strong>of</strong> mammalian syneminwith both vinculin and talin. Coimmunoprecipitation assays show aninteraction <strong>of</strong> synemin with vinculin and talin in cultured rat smoothmuscle cells (A-10 cells). Solid-phase protein-protein binding studies(blot overlays) and in vitro GST pull-down assays demonstrate that aspecific region within mammalian Α-synemin interacts with both vinculinand talin. In addition, colocalization <strong>of</strong> Α-synemin with vinculin andtalin in focal adhesion sites, which contain proteins also present incostameres, was revealed by immun<strong>of</strong>luorescent staining <strong>of</strong> cultured A-10 cells. These results suggest that, via direct interaction with vinculinand talin, the larger Α-synemin is<strong>of</strong>orm appears to function as a linkbetween the heteropolymeric IFs and the costameres located subjacentto the sarcolemma. The heteropolymeric IFs appear to help providemechanical integration <strong>of</strong> the cytoskeleton within mammalian musclecells. (Supported by USDA-CSREES-NRICGP Award 2003-35206-12823)Key Words: My<strong>of</strong>ibrils, Intermediate filaments60 The effect <strong>of</strong> Optaflexx ® dose and feeding duration ongrowth performance <strong>of</strong> steers. M. T. Van Koevering* 1 , A. L.Schroeder 1 , G. J. Vogel 1 , W. J. Platter 1 , A. A. Aguilar 1 , D. Mowrey 1 , S.B. Laudert 1 , G. E. Erickson 2 , R. Pritchard 3 , M. Gaylean 4 , and L. Berger 5 ,1 Elanco <strong>Animal</strong> Health, Greenfield, IN, 2 University <strong>of</strong> Nebraska, Lincoln,3 South Dakota State University, Brookings, 4 Texas Tech University,Lubbock, 5 University <strong>of</strong> Illinois, Urbana.Four studies using 1,867 steers were conducted to evaluate the effects<strong>of</strong> Ractopamine HCL (RAC) on growth performance when fed for thefinal 28, 35 or 42 days (DUR) <strong>of</strong> the finishing period. At each study site,RAC was fed continuously to achieve intake doses <strong>of</strong> approximately 0(CON), 100 (LOW) and 200 (HIGH) mg/hd/d. Each study consisted <strong>of</strong>four to nine replicates for each RAC by DUR combination with 5 to 11steers/pen depending on study site. Analyses <strong>of</strong> growth performancedata were conducted using a linear mixed model procedure, Proc Mixed,SAS v8.2, with pen as the experimental unit. The statistical modelincluded RAC, DUR and RAC x DUR interaction as the independentfixed effects, and study and block within study as random effects. Therewere no RAC x DUR interactions (P>.62). Feed intake for steers fedeither level <strong>of</strong> RAC was not different compared to CON (P>.07). ADGwas greater (P

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