Loss of enigma homolog protein results in dilated cardiomyopathy

谜团同源蛋白的缺失导致扩张型心肌病

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作者:Hongqiang Cheng, Kensuke Kimura, Angela K Peter, Li Cui, Kunfu Ouyang, Tao Shen, Yujie Liu, Yusu Gu, Nancy D Dalton, Sylvia M Evans, Kirk U Knowlton, Kirk L Peterson, Ju Chen

Conclusions

We have identified an ENH-CypherS-Calsarcin protein complex at the Z-line. Ablation of ENH leads to destabilization of this protein complex and dilated cardiomyopathy.

Objective

We studied the role of Enigma homolog protein in the heart using global and cardiac-specific ENH knockout mouse models.

Results

We identified new exons and splice isoforms for ENH in the mouse heart. Impaired cardiac contraction and dilated cardiomyopathy were observed in ENH null mice. Mice with cardiac specific ENH deletion developed a similar dilated cardiomyopathy. Like Cypher, ENH interacted with Calsarcin-1, another Z-line protein. Moreover, biochemical studies showed that ENH, Cypher short isoform and Calsarcin-1 are within the same protein complex at the Z-line. Cypher short isoform and Calsarcin-1 proteins are specifically downregulated in ENH null hearts. Conclusions: We have identified an ENH-CypherS-Calsarcin protein complex at the Z-line. Ablation of ENH leads to destabilization of this protein complex and dilated cardiomyopathy.

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