Gojobori T, Nei M
J Mol Evol. 1981;17(4):245-50. doi: 10.1007/BF01732762.
The nucleotide sequence of a segment of U1 and U3b small RNAs (sRNAs) is shown to have a high complementarity with the nucleotide sequence of a part of the leader region of almost all eukaryotic genes studied so far. The complementary region of U3b is located in the unpaired segment of the secondary structure of U3b constructed by Reddy et al. (1979). A similar complementarity is also observed between these RNAs and the leader regions of eukaryotic viruses, but the complementary region is not always identical with that for eukaryotic genes. Complementarity is also observed between the 3' end of 18S rRNA and a segment of U1 or U3b which is almost contiguous to the region complementary with mRNA. These observations suggest that U1 and U3b may be involved in mRNA processing and transport in the nucleus or in translation in the cytoplasm. In addition to U1 and U3b, another sRNA, i.e., 4.5S RNAI, is shown to have segments which are homologous to the Hogness box of the flanking region of gene and the Proudfoot-Brownlee (PB) box of mRNA near the poly(A) attachment site. The two segments which are complementary with these boxes are located almost contiguously on a co-joined loop of the secondary structure of 4.5S RNAI constructed by Ro-Choi et al. (1972). Since the Hogness box and PB box are both considered as a recognition site by the RNA polymerase, it is possible that 4.5S RNAI is involved in mediating gene transcription.
U1和U3b小RNA(sRNA)片段的核苷酸序列与迄今为止研究的几乎所有真核基因前导区部分的核苷酸序列具有高度互补性。U3b的互补区域位于Reddy等人(1979年)构建的U3b二级结构的未配对片段中。在这些RNA与真核病毒的前导区之间也观察到类似的互补性,但互补区域并不总是与真核基因的互补区域相同。在18S rRNA的3'末端与U1或U3b的一个片段之间也观察到互补性,该片段几乎与与mRNA互补的区域相邻。这些观察结果表明,U1和U3b可能参与细胞核中的mRNA加工和运输或细胞质中的翻译。除了U1和U3b之外,另一种sRNA,即4.5S RNAI,被证明具有与基因侧翼区域的霍格内斯盒以及多聚腺苷酸(poly(A))附着位点附近mRNA的普劳德富特-布朗利(PB)盒同源的片段。与这些盒互补的两个片段几乎连续地位于Ro-Choi等人(1972年)构建的4.5S RNAI二级结构的共同连接环上。由于霍格内斯盒和PB盒都被认为是RNA聚合酶的识别位点,因此4.5S RNAI有可能参与介导基因转录。