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首页> 外文期刊>Current Genetics: Eukaryotes with Emphasis on Yeasts, Fungi, Mitochondria, Plastids >Analysis of manganese-regulated gene expression in the ligninolytic basidiomycete Ceriporiopsis subvermispora.
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Analysis of manganese-regulated gene expression in the ligninolytic basidiomycete Ceriporiopsis subvermispora.

机译:木质素分解担子菌Ceriporiopsis subvermispora中锰调控的基因表达分析。

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摘要

In this work, we explore the use of the unbiased cDNA-AFLP strategy to identify genes involved in Mn(2+) homeostasis in Ceriporiopsis subvermispora. In this ligninolytic white-rot fungus, whose genome has not yet been sequenced, three Mn peroxidase genes responding to Mn(2+) have been characterized. Using cDNA-AFLP to identify transcript-derived fragments (TDFs), a total of 37 differentially expressed cDNA fragments were identified by comparing band intensities among cDNA-AFLP patterns obtained from mycelia from cultures supplemented with different concentrations of Mn(2+). Of 21 differentially expressed TDFs, nine were classified as upregulated, five as downregulated and seven as unregulated. Of these, six upregulated and two downregulated TDFs were selected for further characterization. The expected TDFs for the known Mn peroxidases were not isolated, but several genes encoding proteins related to protein sorting, storage and excretion of excess Mn(2+) were identified. Transcripts induced under Mn(2+) supplementation exhibited homologies to the elongation factor eEF3, a HDEL sequence binding protein and the ARD1 subunit of the N-acetyltransferase complex, among others. Overall, the results obtained in this study suggest a complex picture of Mn(2+) homeostasis and provide the possibility to search for common regulatory elements in the promoters of the novel putatively identified genes.
机译:在这项工作中,我们探索使用无偏的cDNA-AFLP策略来鉴定参与深潜孢子菌Mn(2+)稳态的基因。在这种尚未分解基因组的木质素分解白腐真菌中,已鉴定出响应Mn(2+)的三个Mn过氧化物酶基因。使用cDNA-AFLP来识别转录本片段(TDF),通过比较从菌丝体中添加了不同浓度Mn(2+)的菌丝体获得的cDNA-AFLP模式之间的条带强度,可以鉴定出总共37个差异表达的cDNA片段。在21种差异表达的TDF中,有9种归类为上调,有5种归类为下调,有7种归类为未上调。其中,选择了六个上调的TDF和两个下调的TDF进行进一步表征。没有分离出已知的Mn过氧化物酶的预期TDF,但是鉴定了几种编码与蛋白质分选,储存和排泄过量Mn(2+)相关的​​蛋白质的基因。 Mn(2+)补充下诱导的转录本表现出与延伸因子eEF3,HDEL序列结合蛋白和N-乙酰基转移酶复合物的ARD1亚基的同源性。总体而言,在这项研究中获得的结果表明Mn(2+)动态平衡的复杂的图片,并提供了可能在新型推定的鉴定基因的启动子中搜索常见的调控元件。

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