Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan
J Bacteriol. 2020 Oct 8;202(21). doi: 10.1128/JB.00228-20.
The rare actinomycete forms terminal sporangia containing a few hundred flagellated spores. In response to water, the sporangia open and release the spores into external environments. The orphan response regulator TcrA functions as a global transcriptional activator during sporangium formation and dehiscence. Here, we report the characterization of an orphan hybrid histidine kinase, HhkA. Sporangia of an deletion mutant contained many distorted or ectopically germinated spores and scarcely opened to release the spores under sporangium dehiscence-inducing conditions. These phenotypic changes are quite similar to those observed in a deletion mutant. Comparative RNA sequencing analysis showed that genes controlled by HhkA mostly overlap TcrA-regulated genes. The direct interaction between HhkA and TcrA was suggested by a bacterial two-hybrid assay, but this was not conclusive. The phosphorylation of TcrA using acetyl phosphate as a phosphate donor markedly enhanced its affinity for the TcrA box sequences in the electrophoretic mobility shift assay. Taking these observations together with other results, we proposed that HhkA and TcrA compose a cognate two-component regulatory system, which controls the transcription of the genes involved in many aspects of morphological development, including sporangium formation, spore dormancy, and sporangium dehiscence in goes through complex morphological differentiation, including formation of flagellated spore-containing sporangia, sporangium dehiscence, swimming of zoospores, and germination of zoospores to filamentous growth. Although the orphan response regulator TcrA globally activates many genes required for sporangium formation, spore dormancy, and sporangium dehiscence, its partner histidine kinase remained unknown. Here, we analyzed the function of an orphan hybrid histidine kinase, HhkA, and proposed that HhkA constitutes a cognate two-component regulatory system with TcrA. That HhkA and TcrA homologues are highly conserved among the genus and several closely related rare actinomycetes indicates that this possible two-component regulatory system is employed for complex morphological development in sporangium- and/or zoospore-forming rare actinomycetes.
稀有放线菌形成末端孢子囊,其中含有数百个鞭毛孢子。在对水的响应下,孢子囊打开并将孢子释放到外部环境中。孤儿响应调节剂 TcrA 在孢子囊形成和开裂过程中作为全局转录激活剂发挥作用。在这里,我们报告了一个孤儿杂交组氨酸激酶 HhkA 的特征。缺失突变体的孢子囊包含许多扭曲或异位萌发的孢子,并且在诱导孢子囊开裂的条件下很少打开以释放孢子。这些表型变化与在缺失突变体中观察到的非常相似。比较 RNA 测序分析表明,HhkA 控制的基因主要与 TcrA 调节的基因重叠。细菌双杂交测定表明 HhkA 和 TcrA 之间存在直接相互作用,但这并不具有结论性。使用乙酰磷酸作为磷酸供体对 TcrA 进行磷酸化,在电泳迁移率变动分析中显著增强了其与 TcrA 盒序列的亲和力。将这些观察结果与其他结果结合起来,我们提出 HhkA 和 TcrA 组成一个同源二组分调节系统,该系统控制涉及形态发育许多方面的基因的转录,包括孢子囊形成、孢子休眠和孢子囊开裂在 中经历复杂的形态分化,包括形成含有鞭毛孢子的孢子囊、孢子囊开裂、游动孢子游动和游动孢子萌发为丝状生长。尽管孤儿响应调节剂 TcrA 全局激活了许多孢子囊形成、孢子休眠和孢子囊开裂所需的基因,但它的组氨酸激酶伴侣仍然未知。在这里,我们分析了一个孤儿杂交组氨酸激酶 HhkA 的功能,并提出 HhkA 与 TcrA 构成一个同源二组分调节系统。HhkA 和 TcrA 同源物在属内和几个密切相关的稀有放线菌中高度保守,这表明这个可能的二组分调节系统被用于孢子囊和/或游动孢子形成的稀有放线菌中的复杂形态发育。