Yakkala Harshita Nagasai, Madikonda Ashok Kumar, Behera Sandhya Rani, Pillalamarri Vijaykumar, Mohammad Kashif Gulam, Dhurve Ganeshwari, Tammineni Prasad, Pakala Suresh Babu, Siddavattam Dayananda
Department of Animal Biology, School of Life Sciences, University of Hyderabad, Hyderabad, India.
Department of Biochemistry, School of Life Sciences, University of Hyderabad, Hyderabad, India.
J Biol Chem. 2025 Feb;301(2):108160. doi: 10.1016/j.jbc.2025.108160. Epub 2025 Jan 10.
Noncoding small RNAs are essential for modulating bacterial gene expression, especially under carbon and nutrient-limited conditions. In this study, by using both in silico and molecular hybridization tools, we identified a carbon source responsive small RNA in Acinetobacter baumannii DS002. Expression of corresponding gene, abcR200, located at the intergenic region of omt (O-methyl transferase) and orf72 genes, is under the transcriptional control of a global transcriptional factor, leucine responsive regulatory protein (Lrp). A sequence motif that serves as a target for Lrp was found overlapping the abcR200 promoter (P). Chromatin immunoprecipitation demonstrated that Lrp oligomers, formed under low leucine conditions, strongly interacted to the P. However, the observed interactions were disrupted in the presence of leucine, as leucine promoted dissociation of Lrp to monomers and dimers, the conformation unfavorable to interact with P The abcR200 promoter activity increased with increase of exogenous leucine concentrations, and at 2 mM leucine concentration, maximum promoter activity was observed. The AbcR200 target mRNAs were identified by analyzing the transcriptome of abcR200 negative strain of A. baumannii. Intriguingly, in abcR200 negative background, expression of lut (lactate utilization) mRNA has increased, suggesting lut mRNA as one of the mRNA targets for AbcR200. Consistent of this observation, there existed extensive sequence complementarity between AbcR200 and lut mRNA, especially in the regions coding LutP, LutE, and LutR. In support of the observed sequence complementarity, the levels of lut mRNA encoded proteins got elevated in abcR200 negative HS002 strains suggesting a role for AbcR200 in translational inhibition of lut mRNA.
非编码小RNA对于调节细菌基因表达至关重要,尤其是在碳源和营养受限的条件下。在本研究中,我们通过使用计算机分析和分子杂交工具,在鲍曼不动杆菌DS002中鉴定出一种碳源响应性小RNA。位于omt(O-甲基转移酶)和orf72基因间区的相应基因abcR200的表达受全局转录因子亮氨酸响应调节蛋白(Lrp)的转录控制。发现一个作为Lrp靶标的序列基序与abcR200启动子(P)重叠。染色质免疫沉淀表明,在低亮氨酸条件下形成的Lrp寡聚体与P强烈相互作用。然而,在亮氨酸存在的情况下,观察到的相互作用被破坏,因为亮氨酸促进Lrp解离为单体和二聚体,这种构象不利于与P相互作用。abcR200启动子活性随着外源亮氨酸浓度的增加而增加,在2 mM亮氨酸浓度下观察到最大启动子活性。通过分析鲍曼不动杆菌abcR200阴性菌株的转录组鉴定出AbcR200的靶标mRNA。有趣的是,在abcR200阴性背景下,lut(乳酸利用)mRNA的表达增加,表明lut mRNA是AbcR200的mRNA靶标之一。与这一观察结果一致,AbcR200与lut mRNA之间存在广泛的序列互补性,尤其是在编码LutP、LutE和LutR的区域。为支持观察到的序列互补性,在abcR200阴性HS002菌株中,lut mRNA编码蛋白的水平升高,表明AbcR200在lut mRNA的翻译抑制中发挥作用。