Hirschman J, Wong P K, Sei K, Keener J, Kustu S
Proc Natl Acad Sci U S A. 1985 Nov;82(22):7525-9. doi: 10.1073/pnas.82.22.7525.
In enteric bacteria the products of two nitrogen regulatory genes, ntrA and ntrC, activate transcription of glnA, the structural gene encoding glutamine synthetase, both in vivo and in vitro. The ntrC product (gpntrC) is a DNA-binding protein, which binds to five sites in the glnA promoter-regulatory region and appears to activate transcription initiation. Using as an assay the stimulation of glnA transcription in a coupled in vitro transcription-translation system, we have partially purified the ntrA gene product (gpntrA). The following evidence is consistent with the view that gpntrA is a sigma subunit for RNA polymerase: (i) The gpntrA activity copurifies with the sigma 70 holoenzyme (E sigma 70) and core (E) forms of RNA polymerase through several steps but can be separated from them by chromatography on heparin agarose. (ii) After further purification by molecular sieve chromatography, the partially purified gpntrA fraction allows transcription of glnA from the same startpoint used in vivo; transcription is dependent on gpntrC and on added E. The gpntrA fraction does not allow transcription from promoters that we have used as controls, including lacUV5. E sigma 70 has the reverse specificity.
在肠道细菌中,两个氮调节基因ntrA和ntrC的产物在体内和体外均可激活谷氨酰胺合成酶编码结构基因glnA的转录。ntrC产物(gpntrC)是一种DNA结合蛋白,它与glnA启动子调节区域中的五个位点结合,似乎可激活转录起始。我们使用体外转录-翻译偶联系统中glnA转录的刺激作为检测方法,对ntrA基因产物(gpntrA)进行了部分纯化。以下证据支持gpntrA是RNA聚合酶的一个σ亚基这一观点:(i)gpntrA活性与RNA聚合酶的σ70全酶(Eσ70)和核心(E)形式通过几步共同纯化,但可通过肝素琼脂糖层析将其与它们分离。(ii)通过分子筛层析进一步纯化后,部分纯化的gpntrA组分可从体内使用的相同起始点转录glnA;转录依赖于gpntrC和添加的E。gpntrA组分不允许从我们用作对照的启动子转录,包括lacUV5。Eσ70具有相反的特异性。