Wang B, Korfhagen T R, Gallagher P M, D'Amore M A, McNeish J, Potter S S, Ganschow R E
Division of Basic Science Research, Children's Hospital Research Foundation, Cincinnati, Ohio 45229.
J Biol Chem. 1988 Nov 5;263(31):15841-4.
We have identified and partially characterized a complex transcriptional unit within the murine beta-glucuronidase gene complex on chromosome 5. On the same strand and within the first intron of the beta-glucuronidase structural gene, Gus-s, we observe an RNA polymerase II promoter motif. That sequences within this carefully defined region can promote RNA polymerase II transcription is supported by results of in vitro transcriptional runoff assays and by expression of a linked reporter gene in both cultured cells and transgenic mice. Results of RNA blot hybridization and S1 nuclease protection studies reveal a 2.2-kilobase processed liver transcript which is initiated just downstream of the promoter motif and sharing little, if any, sequence with the 2.7-kilobase beta-glucuronidase mRNA. Both RNA species are found in liver where beta-glucuronidase is known to be expressed in all cell types. To our knowledge, this is the first description of eukaryotic mRNAs from overlapping transcription units which share the same strand yet exhibit little, if any, sequence similarity. A possible regulatory relationship between these overlapping structural genes is discussed.
我们已经在小鼠5号染色体上的β-葡萄糖醛酸酶基因复合体中鉴定出一个复杂的转录单元,并对其进行了部分特征描述。在β-葡萄糖醛酸酶结构基因Gus-s的同一条链上且在其第一个内含子内,我们观察到一个RNA聚合酶II启动子基序。体外转录延伸分析的结果以及在培养细胞和转基因小鼠中连接的报告基因的表达都支持了在这个精确定义区域内的序列能够促进RNA聚合酶II转录这一观点。RNA印迹杂交和S1核酸酶保护研究的结果揭示了一种2.2千碱基的经加工的肝脏转录本,它起始于启动子基序的下游,并且与2.7千碱基的β-葡萄糖醛酸酶mRNA几乎没有序列相似性(如果有的话)。这两种RNA都存在于肝脏中,已知β-葡萄糖醛酸酶在肝脏的所有细胞类型中都有表达。据我们所知,这是对来自重叠转录单元的真核mRNA的首次描述,这些转录单元共享同一条链,但序列相似性很小(如果有的话)。我们还讨论了这些重叠结构基因之间可能的调控关系。