Abstract

Striated muscle tropomyosin (TM) interacts with actin and the troponin complex to regulate calcium-mediated muscle contraction. Previous work by our laboratory established that alpha- and beta-TM isoforms elicit physiological differences in sarcomeric performance. Heart myofilaments containing beta-TM exhibit an increased sensitivity to calcium that is associated with a decrease in the rate of relaxation and a prolonged time of relaxation. To address whether the carboxyl-terminal, troponin T binding domain of beta-TM is responsible for these physiological alterations, we exchanged the 27 terminal amino acids of alpha-TM (amino acids 258 -284) for the corresponding region in beta-TM. Hearts of transgenic mice that express this chimeric TM protein exhibit significant decreases in their rates of contraction and relaxation when assessed by ex vivo work-performing cardiac analyses. There are increases in the time to peak pressure and a dramatic increase in end diastolic pressure. In myofilaments, this chimeric protein induces depression of maximum tension and ATPase rate, together with a significant decrease in sensitivity to calcium. Our data are the first to demonstrate that the TM isoform-specific carboxyl terminus is a critical determinant of sarcomere performance and calcium sensitivity in both the whole heart and in isolated myofilaments.

Highlights

  • Tropomyosin (TM),1 a ␣-helical coiled-coil dimer, plays an essential role in the regulation of contraction and relaxation of the sarcomere

  • This TM sequence was ligated at the 5Ј end to the murine ␣-myosin heavy chain (␣-MHC) promoter, which confers cardiac-specific expression (Fig. 1)

  • When the ␤-TM 3Ј-untranslated region (UTR) sequence is used as a probe, the expression of chimeric TM is seen to be restricted to transgenic heart samples; this probe hybridizes to control skeletal muscle RNA, but it is not detected in NTG cardiac RNA

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Summary

Introduction

Tropomyosin (TM),1 a ␣-helical coiled-coil dimer, plays an essential role in the regulation of contraction and relaxation of the sarcomere. Hearts of transgenic mice that express this chimeric TM protein exhibit significant decreases in their rates of contraction and relaxation when assessed by ex vivo work-performing cardiac analyses.

Results
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