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Structure and Function of SET and MYND Domain-Containing Proteins

机译:SET和MYND结构域蛋白的结构和功能

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摘要

SET (Suppressor of variegation, Enhancer of Zeste, Trithorax) and MYND (Myeloid-Nervy-DEAF1) domain-containing proteins (SMYD) have been found to methylate a variety of histone and non-histone targets which contribute to their various roles in cell regulation including chromatin remodeling, transcription, signal transduction, and cell cycle control. During early development, SMYD proteins are believed to act as an epigenetic regulator for myogenesis and cardiomyocyte differentiation as they are abundantly expressed in cardiac and skeletal muscle. SMYD proteins are also of therapeutic interest due to the growing list of carcinomas and cardiovascular diseases linked to SMYD overexpression or dysfunction making them a putative target for drug intervention. This review will examine the biological relevance and gather all of the current structural data of SMYD proteins.
机译:已发现SET(杂色抑制物,Zeste的增强子,Trithorax)和MYND(髓样神经元DEAF1)域蛋白(SMYD)可以甲基化多种组蛋白和非组蛋白靶标,从而有助于它们在细胞中的各种作用调节,包括染色质重塑,转录,信号转导和细胞周期控制。在早期发育过程中,由于SMYD蛋白在心肌和骨骼肌中大量表达,因此被认为是肌生成和心肌细胞分化的表观遗传调节剂。由于与SMYD过表达或功能障碍有关的癌症和心血管疾病的清单越来越多,因此SMYD蛋白也具有治疗意义,使其成为药物干预的靶标。这项审查将检查生物学相关性,并收集SMYD蛋白的所有当前结构数据。

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