Van Arsdell S W, Weiner A M
Mol Cell Biol. 1984 Mar;4(3):492-9. doi: 10.1128/mcb.4.3.492-499.1984.
We found that the genes for human U2 small nuclear RNA (snRNA) are organized as a nearly perfect tandem array of 10 to 20 copies per haploid genome. Although the coding region for the mature form of U2 RNA was only 188 base pairs (bp) long, the basic repeating unit of the tandem array was 6 kilobase pairs in length. Comparison of DNA sequences immediately upstream from human U1 and U2 genes revealed two regions of strong homology: region I (15 bp long) lay upstream of region II (20 bp long) and was separated from it by about the same distance in U1 genes (25 bp) as in U2 genes (21 bp); however, region I and region II were located 174 bp further upstream from the 5' end of the snRNA coding sequence in U1 genes than in U2 genes. Homologs of region II were also found upstream of the snRNA coding region in a mouse U2 gene and two rat U1 genes. Murphy et al. (Cell 29:265-274, 1982) have found that sequences within region II may function as the equivalent of a TATA box for initiation by RNA polymerase II in vitro at a position 183 bp upstream from the 5' end of the human U1 snRNA coding region. In light of the data reported here, this result suggests that region II does indeed play a role in transcription but that its position relative to the actual initiation site can vary.
我们发现,人类U2小核RNA(snRNA)的基因以近乎完美的串联阵列形式组织,每个单倍体基因组中有10至20个拷贝。尽管U2 RNA成熟形式的编码区只有188个碱基对(bp)长,但串联阵列的基本重复单元长度为6千碱基对。对人类U1和U2基因上游紧邻的DNA序列进行比较,发现了两个高度同源的区域:区域I(15 bp长)位于区域II(20 bp长)的上游,在U1基因中它与区域II的间隔距离(25 bp)与在U2基因中(21 bp)大致相同;然而,区域I和区域II在U1基因中距离snRNA编码序列5'端的上游比在U2基因中远174 bp。在小鼠U2基因和两个大鼠U1基因的snRNA编码区上游也发现了区域II的同源物。墨菲等人(《细胞》29:265 - 274,1982)发现,区域II内的序列可能在体外相当于一个TATA盒,用于RNA聚合酶II在人类U1 snRNA编码区5'端上游183 bp处起始转录。根据此处报告的数据,这一结果表明区域II确实在转录中起作用,但其相对于实际起始位点的位置可能会有所不同。