Theissen H, Rinke J, Traver C N, Lührmann R, Appel B
Gene. 1985;36(1-2):195-9. doi: 10.1016/0378-1119(85)90086-1.
A genomic DNA library containing human placental DNA cloned into phage lambda Charon 4A was screened for snRNA U6 genes. In vitro 32P-labeled U6 snRNA isolated from HeLa cells was used as a hybridization probe. A positive clone containing a 4.6-kb EcoRI fragment of human chromosomal DNA was recloned into the EcoRI site of pBR325 and mapped by restriction endonuclease digestion. Restriction fragments containing U6 RNA sequences were identified by hybridization with isolated U6[32P]RNA. The sequence analysis revealed a novel structure of a U6 RNA pseudogene, bearing two 17-nucleotide(nt)-long direct repeats of genuine U6 RNA sequences arranged in a head-to-tail fashion within the 5' part of the molecule. Hypothetical models as to how this type of snRNA U6 pseudogene might have been generated during evolution of the human genome are presented. When compared to mammalian U6 RNA sequences the pseudogene accounts for a 77% overall sequence homology and contains the authentic 5'- and 3'-ends of the U6 RNA.
为筛选snRNA U6基因,对一个将人胎盘DNA克隆到噬菌体λCharon 4A中的基因组DNA文库进行了筛选。从HeLa细胞中分离出的体外32P标记的U6 snRNA用作杂交探针。将一个包含4.6 kb人染色体DNA的EcoRI片段的阳性克隆重新克隆到pBR325的EcoRI位点,并通过限制性内切酶消化进行图谱绘制。通过与分离出的U6[32P]RNA杂交鉴定出含有U6 RNA序列的限制性片段。序列分析揭示了U6 RNA假基因的一种新结构,在分子的5'部分内有两个17个核苷酸(nt)长的真正U6 RNA序列的同向重复序列,呈头对尾排列。本文提出了关于这种类型的snRNA U6假基因在人类基因组进化过程中可能如何产生的假设模型。与哺乳动物U6 RNA序列相比,该假基因的总体序列同源性为77%,并包含U6 RNA真实的5'和3'末端。