Segade F, Hurlé B, Claudio E, Ramos S, Lazo P S
Departamento de Bioquímica y Biología Molecular, Universidad de Oviedo, Spain.
FEBS Lett. 1996 Jun 3;387(2-3):152-6. doi: 10.1016/0014-5793(96)00496-6.
We report the identification of a mouse cDNA, SIG41, encoding a protein of 288 amino acids that is 45% identical (58% similar) to the Drosophila splicing regulator Tra2. SIG41 cDNA contains four polyadenylation signals whose alternative use gives rise to four types of transcripts (2.1, 2.0, 1.5, and 1.4 kb) in mouse cells. Northern analysis and RT-PCR assays showed that SIG41 mRNA is present in virtually all the cell lines and tissues studied, with remarkable levels of expression in uterus and brain tissues. Differential stability of the SIG41 mRNAs was detected in mouse macrophage cells.
我们报告了一种小鼠cDNA(SIG41)的鉴定,它编码一种由288个氨基酸组成的蛋白质,该蛋白质与果蝇剪接调节因子Tra2有45%的同一性(58%的相似性)。SIG41 cDNA包含四个聚腺苷酸化信号,其交替使用在小鼠细胞中产生四种类型的转录本(2.1、2.0、1.5和1.4 kb)。Northern分析和RT-PCR检测表明,SIG41 mRNA几乎存在于所有研究的细胞系和组织中,在子宫和脑组织中表达水平显著。在小鼠巨噬细胞中检测到SIG41 mRNA的差异稳定性。