
The nucleotide sequence of U11 small nuclear RNA, a minor U RNA from HeLa cells, was determined. Computer analysis of the sequence (135 residues) predicts two strong hairpin loops which are separated by seventeen nucleotides containing an Sm binding site (AAUUUUUUGG). A synthetic gene was constructed in which the coding region of U11 RNA is under the control of a T7 promoter. This vector can be used to produce U11 RNA in vitro. Southern hybridization and PCR analysis of HeLa genomic DNA suggest that U11 RNA is encoded by a single copy gene, and that at least three genomic regions could be U11 RNA pseudogenes. A HeLa genomic copy of a U11 gene was isolated by inverted PCR. This gene contains the U11 RNA coding sequence and several sequence elements unique for the U RNA genes. These include a Distal Sequence Element (DSE, ATTTGCATA) present between positions -215 and -223 relative to the start of transcription; a Proximal Sequence Element (PSE, TTCACCTTTACCAAAAATG) located between positions -43 and -63; and a 3' box (GTTAGGCGAAATATTA) between positions + 150 and + 166. Transfection of HeLa cells with this gene revealed that it is functioning in vivo and can produce U11 RNA.
Genomic Library, Base Sequence, Molecular Sequence Data, Gene Expression, Nucleic Acid Hybridization, Transfection, Polymerase Chain Reaction, RNA, Small Nuclear, Humans, Cloning, Molecular, Pseudogenes, HeLa Cells
Genomic Library, Base Sequence, Molecular Sequence Data, Gene Expression, Nucleic Acid Hybridization, Transfection, Polymerase Chain Reaction, RNA, Small Nuclear, Humans, Cloning, Molecular, Pseudogenes, HeLa Cells
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