Rothermel B, Vega R B, Yang J, Wu H, Bassel-Duby R, Williams R S
Departments of Internal Medicine and Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390-8573, USA.
J Biol Chem. 2000 Mar 24;275(12):8719-25. doi: 10.1074/jbc.275.12.8719.
Here we describe a small family of proteins, termed MCIP1 and MCIP2 (for myocyte-enriched calcineurin interacting protein), that are expressed most abundantly in striated muscles and that form a physical complex with calcineurin A. MCIP1 is encoded by DSCR1, a gene located in the Down syndrome critical region. Expression of the MCIP family of proteins is up-regulated during muscle differentiation, and their forced overexpression inhibits calcineurin signaling to a muscle-specific target gene in a myocyte cell background. Binding of MCIP1 to calcineurin A requires sequence motifs that resemble calcineurin interacting domains found in NFAT proteins. The inhibitory action of MCIP1 involves a direct association with the catalytic domain of calcineurin, rather than interference with the function of downstream components of the calcineurin signaling pathway. The interaction between MCIP proteins and calcineurin may modulate calcineurin-dependent pathways that control hypertrophic growth and selective programs of gene expression in striated muscles.
在此,我们描述了一个小的蛋白质家族,称为MCIP1和MCIP2(肌细胞富集的钙调神经磷酸酶相互作用蛋白),它们在横纹肌中表达最为丰富,并与钙调神经磷酸酶A形成物理复合物。MCIP1由DSCR1编码,DSCR1是位于唐氏综合征关键区域的一个基因。MCIP蛋白家族的表达在肌肉分化过程中上调,其强制过表达在肌细胞背景下抑制钙调神经磷酸酶向肌肉特异性靶基因的信号传导。MCIP1与钙调神经磷酸酶A的结合需要类似于在NFAT蛋白中发现的钙调神经磷酸酶相互作用结构域的序列基序。MCIP1的抑制作用涉及与钙调神经磷酸酶催化结构域的直接结合,而不是干扰钙调神经磷酸酶信号通路下游成分的功能。MCIP蛋白与钙调神经磷酸酶之间的相互作用可能调节控制横纹肌肥大生长和基因表达选择性程序的钙调神经磷酸酶依赖性途径。