Ames P, Parkinson J S
Biology Department, University of Utah, Salt Lake City 84112.
J Bacteriol. 1994 Oct;176(20):6340-8. doi: 10.1128/jb.176.20.6340-6348.1994.
Tsr, the serine chemoreceptor of Escherichia coli, has two signaling modes. One augments clockwise (CW) flagellar rotation, and the other augments counterclockwise (CCW) rotation. To identify the portion of the Tsr molecule responsible for these activities, we isolated soluble fragments of the Tsr cytoplasmic domain that could alter the flagellar rotation patterns of unstimulated wild-type cells. Residues 290 to 470 from wild-type Tsr generated a CW signal, whereas the same fragment with a single amino acid replacement (alanine 413 to valine) produced a CCW signal. The soluble components of the chemotaxis phosphorelay system needed for expression of these Tsr fragment signals were identified by epistasis analysis. Like full-length receptors, the fragments appeared to generate signals through interactions with the CheA autokinase and the CheW coupling factor. CheA was required for both signaling activities, whereas CheW was needed only for CW signaling. Purified Tsr fragments were also examined for effects on CheA autophosphorylation activity in vitro. Consistent with the in vivo findings, the CW fragment stimulated CheA, whereas the CCW fragment inhibited CheA. CheW was required for stimulation but not for inhibition. These findings demonstrate that a 180-residue segment of the Tsr cytoplasmic domain can produce two active signals. The CCW signal involves a direct contact between the receptor and the CheA kinase, whereas the CW signal requires participation of CheW as well. The correlation between the in vitro effects of Tsr signaling fragments on CheA activity and their in vivo behavioral effects lends convincing support to the phosphorelay model of chemotactic signaling.
Tsr是大肠杆菌的丝氨酸化学感受器,具有两种信号传导模式。一种增强顺时针(CW)鞭毛旋转,另一种增强逆时针(CCW)旋转。为了确定Tsr分子中负责这些活性的部分,我们分离了Tsr细胞质结构域的可溶性片段,这些片段可以改变未受刺激的野生型细胞的鞭毛旋转模式。野生型Tsr的290至470位残基产生CW信号,而具有单个氨基酸替换(丙氨酸413替换为缬氨酸)的相同片段产生CCW信号。通过上位性分析确定了这些Tsr片段信号表达所需的趋化磷酸传递系统的可溶性成分。与全长受体一样,这些片段似乎通过与CheA自激酶和CheW偶联因子相互作用产生信号。两种信号传导活性都需要CheA,而CW信号传导仅需要CheW。还检测了纯化的Tsr片段对体外CheA自磷酸化活性的影响。与体内研究结果一致,CW片段刺激CheA,而CCW片段抑制CheA。刺激需要CheW,但抑制不需要。这些发现表明,Tsr细胞质结构域的一个180个残基的片段可以产生两种活性信号。CCW信号涉及受体与CheA激酶之间的直接接触,而CW信号也需要CheW的参与。Tsr信号片段对CheA活性的体外影响与其体内行为影响之间的相关性为趋化信号传导的磷酸传递模型提供了令人信服的支持。