He B, Kukarin A, Temiakov D, Chin-Bow S T, Lyakhov D L, Rong M, Durbin R K, McAllister W T
Department of Microbiology and Immunology, Morse Institute for Molecular Genetics, State University of New York, Health Science Center, Brooklyn, New York 11203-2098, USA.
J Biol Chem. 1998 Jul 24;273(30):18802-11. doi: 10.1074/jbc.273.30.18802.
We have characterized an unusual type of termination signal for T7 RNA polymerase that requires a conserved 7-base pair sequence in the DNA (ATCTGTT in the non-template strand). Each of the nucleotides within this sequence is critical for function, as any substitutions abolish termination. The primary site of termination occurs 7 nucleotides downstream from this sequence but is context-independent (that is, the sequence around the site of termination, and in particular the nucleotide at the site of termination, need not be conserved). Termination requires the presence of the conserved sequence and its complement in duplex DNA and is abolished or diminished if the signal is placed downstream of regions in which the non-template strand is missing or mismatched. Under the latter conditions, much of the RNA product remains associated with the template. The latter results suggest that proper resolution of the transcription bubble at its trailing edge and/or displacement of the RNA product are required for termination at this class of signal.
我们已经鉴定出一种不同寻常的T7 RNA聚合酶终止信号,它需要DNA中一段保守的7个碱基对序列(非模板链上为ATCTGTT)。该序列中的每个核苷酸对功能都至关重要,因为任何替换都会消除终止作用。终止的主要位点位于该序列下游7个核苷酸处,但与上下文无关(即终止位点周围的序列,特别是终止位点处的核苷酸,无需保守)。终止需要双链DNA中存在保守序列及其互补序列,如果该信号位于非模板链缺失或错配区域的下游,则终止作用会被消除或减弱。在后一种情况下,许多RNA产物仍与模板结合。后一种结果表明,在这类信号处终止需要转录泡在其后缘正确解离和/或RNA产物移位。