Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
J Biol Chem. 2012 Oct 26;287(44):37362-70. doi: 10.1074/jbc.M112.364927. Epub 2012 Sep 12.
Human slow skeletal troponin T (HSSTnT) shares a high degree of homology with cardiac TnT (CTnT). Although the presence of HSSTnT has not been confirmed in the heart at the protein level, detectable levels of HSSTnT mRNA have been found. Whether HSSTnT isoforms are expressed transiently remains unknown. Because transient re-expression of HSSTnT may be a potential mechanism of regulating function, we explored the effect of HSSTnT on the regulation of cardiac muscle. At least three HSSTnT isoforms have been found to exist in slow skeletal muscle: HSSTnT1 (+exons 5 and 12), HSSTnT2 (+exon 5, -exon 12), and HSSTnT3 (-exons 5 and 12). Another isoform, HSSTnT hypothetical (Hyp) (-exon 5, +exon 12), has only been found at the mRNA level. Compared with HCTnT3 (adult isoform), Tn complexes containing HSSTnT1, -2, and -3 did not alter the actomyosin ATPase activation and inhibition in the presence and absence of Ca(2+), respectively. HSSTnTHyp was not evaluated as it did not form a Tn complex under a variety of conditions. Porcine papillary skinned fibers displaced with HSSTnT1, -2, or -3 and reconstituted with human cardiac troponin I and troponin C (HCTnI·TnC) complex showed a decrease in the Ca(2+) sensitivity of force development and an increase in maximal recovered force (HSSTnT1 and -3) compared with HCTnT3. In contrast, HSSTnTHyp showed an increase in the Ca(2+) sensitivity of force development. This suggests that re- or overexpression of specific SSTnT isoforms might have therapeutic potential in the failing heart because they increase the maximal force of contraction. In addition, circular dichroism and proteolytic digestion experiments revealed structural differences between HSSTnT isoforms and HCTnT3 and that HSSTnT1 is more susceptible to calpain and trypsin proteolysis than the other HSSTnTs. Overall, HSSTnT isoforms despite being homologues of CTnT may display distinct functional properties in muscle regulation.
人类慢肌肌钙蛋白 T(HSSTnT)与心肌肌钙蛋白 T(CTnT)具有高度同源性。尽管在蛋白质水平上尚未确认 HSSTnT 存在于心内,但已发现可检测水平的 HSSTnT mRNA。HSSTnT 同工型是否短暂表达尚不清楚。由于 HSSTnT 的瞬时再表达可能是调节功能的潜在机制,因此我们探讨了 HSSTnT 对心肌调节的影响。在慢肌中已发现至少三种 HSSTnT 同工型存在:HSSTnT1(+外显子 5 和 12)、HSSTnT2(+外显子 5,-外显子 12)和 HSSTnT3(-外显子 5 和 12)。另一种同工型 HSSTnT 假说(Hyp)(-外显子 5,+外显子 12)仅在 mRNA 水平上发现。与 HCTnT3(成人同工型)相比,分别在存在和不存在 Ca2+的情况下,含有 HSSTnT1、-2 和 -3 的 Tn 复合物并未改变肌动球蛋白 ATP 酶的激活和抑制。由于在各种条件下 HSSTnTHyp 均未形成 Tn 复合物,因此未对其进行评估。用 HSSTnT1、-2 或 -3 置换猪乳头肌去皮纤维并与人心肌肌钙蛋白 I 和肌钙蛋白 C(HCTnI·TnC)复合物重新构成,与 HCTnT3 相比,显示出力发展的 Ca2+敏感性降低和最大恢复力增加(HSSTnT1 和 -3)。相比之下,HSSTnTHyp 显示出力发展的 Ca2+敏感性增加。这表明,特定 SSTnT 同工型的重新表达或过表达可能在心力衰竭中有治疗潜力,因为它们增加了收缩的最大力。此外,圆二色性和蛋白水解消化实验揭示了 HSSTnT 同工型与 HCTnT3 之间的结构差异,并且 HSSTnT1 比其他 HSSTnTs 更容易受到钙蛋白酶和胰蛋白酶的蛋白水解。总体而言,尽管 HSSTnT 同工型是 CTnT 的同源物,但在肌肉调节中可能表现出不同的功能特性。