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鉴定六价铬诱导的假单胞菌 Cr13 差异表达基因。

Identification of differentially expressed genes for Pseudomonas sp. Cr13 stimulated by hexavalent chromium.

机构信息

College of Life Science, Guangxi Normal University, Guilin, China.

Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection (Guangxi Normal University), Ministry of Education, Guilin, China.

出版信息

PLoS One. 2022 Aug 5;17(8):e0272528. doi: 10.1371/journal.pone.0272528. eCollection 2022.

Abstract

Over exploitation of mineral resources has increasingly caused serious heavy metal contamination such as chromium (Cr). Cr(VI), the pathogenicity factor, is one of common environmental contaminants and widely known health hazards to living organisms. Therefore, it is urgent to control the polluted soil. Up to now, little is known about the regulatory mechanisms of Cr response in Pseudomonas sp. Cr13. In this study, transcriptome and differentially expressed genes in Pseudomonas sp. Cr13 strain was characterized by a comparison between Cr(VI)-treated sample and control sample using transcriptome sequencing approach. In total, 2974 genes were annotated, including 1245 (1154 down-regulated genes and 91 up-regulated genes) differentially expressed genes (DEGs). All DEGs could be assigned to 29 pathways, of which pathways related to amino acid metabolism, carbohydrate metabolism, energy metabolism and signal transduction mechanism were significantly enriched in Pseudomonas sp. Cr13. A possible mechanism for Cr toxicity response might be an active efflux which utilized a heavy metal translocating P-type ATPase to lower the intracellular Cr concentration. The down-regulated genes related to the antioxidant defense system had a key role in Cr reduction, such as SodA, Gst, osmC, BtuE, KatE, csdA and AhpC. The proteins that were visibly up-regulated, were likely to involve in alleviating Cr(VI) stress, and the significantly down-regulated genes such as MarR, Lrp, FhlA, GntR, HrcA, LysR family genes, were likely to reduce Cr(VI) induced oxidative stress. In addition, real-time quantitative PCR was used to analyze the expression patterns of some Cr responsive genes. This study reported the first identification of Cr responsive genes, and inferred the underlying regulatory mechanisms of response to Cr(VI) stress in Pseudomonas sp. Cr13.

摘要

矿产资源的过度开采导致了严重的重金属污染,如铬(Cr)。Cr(VI)是一种致病因子,是常见的环境污染物之一,对生物有广泛的危害。因此,控制污染土壤迫在眉睫。到目前为止,关于假单胞菌 Cr13 对 Cr 响应的调控机制知之甚少。在本研究中,通过转录组测序方法,比较 Cr(VI)处理样品和对照样品,对假单胞菌 Cr13 菌株的转录组和差异表达基因进行了表征。总共注释了 2974 个基因,包括 1245 个(1154 个下调基因和 91 个上调基因)差异表达基因(DEGs)。所有 DEGs 可被分配到 29 条途径,其中与氨基酸代谢、碳水化合物代谢、能量代谢和信号转导机制相关的途径在假单胞菌 Cr13 中显著富集。Cr 毒性响应的可能机制是一种主动外排,利用重金属转运 P 型 ATP 酶降低细胞内 Cr 浓度。与抗氧化防御系统相关的下调基因在 Cr 还原中起关键作用,如 SodA、Gst、osmC、BtuE、KatE、csdA 和 AhpC。明显上调的蛋白质可能参与缓解 Cr(VI)胁迫,而下调的基因如 MarR、Lrp、FhlA、GntR、HrcA、LysR 家族基因可能减少 Cr(VI)诱导的氧化应激。此外,还使用实时定量 PCR 分析了一些 Cr 响应基因的表达模式。本研究首次报道了 Cr 响应基因的鉴定,并推断了假单胞菌 Cr13 对 Cr(VI)胁迫响应的潜在调控机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a4f/9355187/2f346baa72b3/pone.0272528.g001.jpg

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