Franco del Amo F, Gendron-Maguire M, Swiatek P J, Gridley T
Department of Cell and Developmental Biology, Roche Institute of Molecular Biology, Nutley, NJ.
Biochim Biophys Acta. 1993 Jan 23;1171(3):323-7. doi: 10.1016/0167-4781(93)90076-p.
We describe the cloning of a full length cDNA encoding the mouse mammalian achaete-scute homolog 1 (mouse MASH1). Using a ribonuclease protection assay to examine expression of this gene in cell lines, postimplantation embryos and adult tissues, expression was detected between days 10.5 and 16.5 of gestation and in adult brain. No expression was detected in other adult tissues or in most of the cell lines examined. However, differentiation of P19 embryonal carcinoma cells into neuronal cell types by exposure to retinoic acid resulted in the induction of MASH1 RNA expression.
我们描述了编码小鼠哺乳动物无刚毛-缺刻同源物1(小鼠MASH1)的全长cDNA的克隆过程。使用核糖核酸酶保护试验来检测该基因在细胞系、植入后胚胎和成年组织中的表达,在妊娠第10.5天至16.5天之间以及成年大脑中检测到了表达。在其他成年组织或所检测的大多数细胞系中未检测到表达。然而,通过暴露于视黄酸将P19胚胎癌细胞分化为神经元细胞类型会导致MASH1 RNA表达的诱导。