Kress H, Tönjes R, Doenecke D
Nucleic Acids Res. 1986 Sep 25;14(18):7189-97. doi: 10.1093/nar/14.18.7189.
Sodium butyrate was used to induce the accumulation of human H1(0) mRNA in HeLa cells. The length of this mRNA (2,300 nucleotides) was determined by Northern blot hybridization and S1 nuclease analysis using a human H1(0) gene probe. The mRNA shows long 5' and 3' non coding segments and it is polyadenylated. The signal for this step of mRNA maturation (cleavage and polyadenylation) appears to be the hexanucleotide AAUAAA in analogy to most (other than histone) mRNA species. Thus, the mode of maturation of H1(0) mRNA differs, on one hand, from that of the cell cycle dependent mRNA species, where it is based on a specific stem-and-loop structure. On the other hand, the 3' end of H1(0) mRNA varies from H5 mRNA, which is characterized by two unique dyad symmetry structures at its 3' end.
丁酸钠用于诱导HeLa细胞中人类H1(0) mRNA的积累。使用人类H1(0)基因探针,通过Northern印迹杂交和S1核酸酶分析确定了该mRNA的长度(2300个核苷酸)。该mRNA具有较长的5'和3'非编码区,并且是多聚腺苷酸化的。与大多数(组蛋白除外)mRNA种类类似,这一步骤的mRNA成熟信号(切割和多聚腺苷酸化)似乎是六核苷酸AAUAAA。因此,H1(0) mRNA的成熟模式一方面不同于依赖细胞周期的mRNA种类,后者基于特定的茎环结构。另一方面,H1(0) mRNA的3'端与H5 mRNA不同,H5 mRNA在其3'端具有两个独特的二重对称结构。