Ghosh B, Grzadzielska E, Bhattacharya P, Peralta E, DeVito J, Das A
Department of Microbiology, University of Connecticut Health Center, Farmington 06030.
J Mol Biol. 1991 Nov 5;222(1):59-66. doi: 10.1016/0022-2836(91)90737-q.
Transcription of the ribosomal RNA operons (rrn) in Escherichia coli is subject to an antitermination mechanism whereby RNA polymerase is modified to a termination-resistant form during transit through the rrn leader region. This antitermination mechanism is unable to overcome the T1-T2 terminator cluster located at the end of an rrn operon, such as rrnB. We have tested the specificity with which the T1-T2 terminators override an antitermination mechanism, by placing the terminator cluster downstream from the nut and qut sites recognized by phage lambda N and Q gene antiterminators, respectively. Measurement of downstream gene expression shows that RNA polymerase modified by either N or Q reads through the T1-T2 terminators quite efficiently. This supports the view that T1-T2 are not superterminators, and that the rrn antitermination mechanism may have a restricted terminator specificity.
大肠杆菌核糖体RNA操纵子(rrn)的转录受抗终止机制调控,即RNA聚合酶在穿过rrn前导区时被修饰为抗终止形式。这种抗终止机制无法克服位于rrn操纵子末端(如rrnB)的T1-T2终止子簇。我们通过将终止子簇分别置于噬菌体λ N和Q基因抗终止子识别的nut和qut位点下游,测试了T1-T2终止子超越抗终止机制的特异性。对下游基因表达的测量表明,被N或Q修饰的RNA聚合酶能够相当有效地通读T1-T2终止子。这支持了T1-T2不是超级终止子的观点,并且rrn抗终止机制可能具有有限的终止子特异性。