O'Connor L, Tangney M, Fitzgerald GF
Department of Microbiology and National Food Biotechnology Centre, University College, Cork, Ireland.
Appl Environ Microbiol. 1999 Jan;65(1):330-5. doi: 10.1128/AEM.65.1.330-335.1999.
The abortive infection system AbiG is encoded by the lactococcal plasmid pCI750. The abiG locus (consisting of two genes, abiGi and abiGii) was examined by Northern blot analysis, revealing two transcripts of approximately 2.8 and 1.5 kb which were homologous to the two gene-specific probes. A transcriptional start site was mapped upstream of abiGi, and it appeared that the two genes were cotranscribed, resulting in the 2.8-kb transcript. The smaller transcript may be the result of independent transcription of abiGii within abiGi or of the presence of a weak terminator within abiGii. The locus was shown to be constitutively expressed. Evidence is presented for the possible existence of a second Abi mechanism on pCI750. Examination of phage sk1 RNA synthesis demonstrated that both the subcloned AbiG and, to a greater extent, pCI750 inhibited this process. pCI750 also severely inhibited synthesis of both early and late phage c2 transcripts, while the presence of the subclone resulted in a reduction in late transcript synthesis only.
流产感染系统AbiG由乳球菌质粒pCI750编码。通过Northern印迹分析检测abiG位点(由abiGi和abiGii两个基因组成),发现了与两个基因特异性探针同源的大约2.8 kb和1.5 kb的两种转录本。转录起始位点定位于abiGi上游,似乎这两个基因是共转录的,产生了2.8 kb的转录本。较小的转录本可能是abiGii在abiGi内独立转录的结果,或者是abiGii内存在弱终止子的结果。该位点显示为组成型表达。有证据表明pCI750上可能存在第二种Abi机制。对噬菌体sk1 RNA合成的检测表明,亚克隆的AbiG以及在更大程度上pCI750均抑制了这一过程。pCI750也严重抑制了噬菌体c2早期和晚期转录本的合成,而亚克隆的存在仅导致晚期转录本合成减少。