Tapscott S J, Davis R L, Thayer M J, Cheng P F, Weintraub H, Lassar A B
Department of Genetics, Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
Science. 1988 Oct 21;242(4877):405-11. doi: 10.1126/science.3175662.
Expression of a complementary DNA (cDNA) encoding the mouse MyoD1 protein in a variety of fibroblast and adipoblast cell lines converts them to myogenic cells. Polyclonal antisera to fusion proteins containing the MyoD1 sequence show that MyoD1 is a phosphoprotein present in the nuclei of proliferating myoblasts and differentiated myotubes but not expressed in 10T1/2 fibroblasts or other nonmuscle cell types. Functional domains of the MyoD1 protein were analyzed by site-directed deletional mutagenesis of the MyoD1 cDNA. Deletion of a highly basic region (residues 102 to 135) interferes with both nuclear localization and induction of myogenesis. Deletion of a short region (residues 143 to 162) that is similar to a conserved region in the c-Myc family of proteins eliminates the ability of the MyoD1 protein to initiate myogenesis but does not alter nuclear localization. Deletions of regions spanning the remainder of MyoD1 did not affect nuclear localization and did not inhibit myogenesis. Furthermore, expression of only 68 amino acids of MyoD1, containing the basic and the Myc similarity domains, is sufficient to activate myogenesis in stably transfected 10T1/2 cells. Genetic analysis maps the MyoD1 gene to mouse chromosome 7 and human chromosome 11.
在多种成纤维细胞和脂肪母细胞系中表达编码小鼠肌分化蛋白1(MyoD1)的互补DNA(cDNA)可将它们转化为肌原性细胞。针对包含MyoD1序列的融合蛋白的多克隆抗血清显示,MyoD1是一种磷蛋白,存在于增殖的成肌细胞和分化的肌管的细胞核中,但在10T1/2成纤维细胞或其他非肌肉细胞类型中不表达。通过对MyoD1 cDNA进行定点缺失诱变分析了MyoD1蛋白的功能结构域。缺失一个高度碱性区域(第102至135位氨基酸)会干扰核定位和肌生成诱导。缺失一个与c-Myc蛋白家族保守区域相似的短区域(第143至162位氨基酸)会消除MyoD1蛋白启动肌生成的能力,但不会改变核定位。缺失MyoD1其余部分的区域不会影响核定位,也不会抑制肌生成。此外,仅表达包含碱性和Myc相似结构域的68个氨基酸的MyoD1就足以在稳定转染的10T1/2细胞中激活肌生成。遗传分析将MyoD1基因定位到小鼠7号染色体和人类11号染色体。