Lea I, Moore H D, Latchman D S
Department of Biochemistry, University College and Middlesex School of Medicine, London, U.K.
Biochem J. 1991 Aug 1;277 ( Pt 3)(Pt 3):719-22. doi: 10.1042/bj2770719.
The mouse U1b SnRNA gene is expressed in only a limited range of cell types, whereas the U1a SnRNA gene is expressed in all cells. These two genes differ in the sequence of the octamer motif, which plays a critical role in SnRNA gene regulation. We show that the U1b octamer binds the octamer-binding protein Oct-1 with higher affinity than does the U1a octamer in both U1b-expressing and -non-expressing cell lines and tissues. Moreover, the U1b octamer can direct a higher level of gene expression than the U1a octamer when linked to a heterologous promoter and introduced into a non-U1b-expressing cell line. Hence the tissue-specific expression of the U1b gene is not determined by the failure of its octamer motif to bind Oct-1 or the weak affinity of this binding.
小鼠U1b SnRNA基因仅在有限的细胞类型范围内表达,而U1a SnRNA基因在所有细胞中均有表达。这两个基因在八聚体基序的序列上存在差异,该基序在SnRNA基因调控中起关键作用。我们发现,在表达U1b和不表达U1b的细胞系及组织中,U1b八聚体与八聚体结合蛋白Oct-1的结合亲和力均高于U1a八聚体。此外,当与异源启动子相连并导入不表达U1b的细胞系时,U1b八聚体能够比U1a八聚体指导更高水平的基因表达。因此,U1b基因的组织特异性表达并非由其八聚体基序无法结合Oct-1或这种结合的弱亲和力所决定。