Sado Takashi, Nakajima Noboru, Tada Masako, Takagi Nobuo
Research Center for Molecular Genetics and Division of Biological Science, Graduate School of Environmental Earth Science.
Department of Chemistry II, Faculty of Science, Hokkaido University, Sapporo 060, Japan.
Dev Growth Differ. 1993 Oct;35(5):551-560. doi: 10.1111/j.1440-169X.1993.00551.x.
A novel mesoderm-specific cDNA clone has been isolated by differential screening of cDNA library from an embryonal carcinoma (EC) cell line MC12. The cDNA clone 121a is about 2.5 kb in length and apparently encodes a putative polypeptide of 335 amino acids which may be secreted or membrane anchored glycoprotein since it has a possible signal sequence and a potential N-linked glycosylation site. In situ hybridization using mouse embryos revealed that 121a expression was confined to mesoderm and its derivatives such as allantois, the mesodermal layer of amnion, chorion and yolk sac, somites, heart, etc. These findings suggest that 121 a may be essential for mesodermal differentiation or function, although nothing definite is known. Conservation of 121a homolog in mammals and even in Drosophila seems to support this presumption. Fluorescence in situ hybridization successfully localized 121a to B1 band of mouse chromosome 6.
通过对胚胎癌细胞系MC12的cDNA文库进行差异筛选,分离出了一个新的中胚层特异性cDNA克隆。cDNA克隆121a长度约为2.5 kb,显然编码一个335个氨基酸的假定多肽,由于它有一个可能的信号序列和一个潜在的N-连接糖基化位点,可能是分泌型或膜锚定糖蛋白。使用小鼠胚胎进行原位杂交显示,121a的表达局限于中胚层及其衍生物,如尿囊、羊膜、绒毛膜和卵黄囊的中胚层、体节、心脏等。这些发现表明,121a可能对中胚层分化或功能至关重要,尽管目前尚无定论。121a同源物在哺乳动物甚至果蝇中的保守性似乎支持了这一推测。荧光原位杂交成功地将121a定位到小鼠6号染色体的B1带。