首页> 外文期刊>Mycological progress >Differential gene expression in Alternaria gaisen exposed to dark andTI Differential gene expression in Alternaria gaisen exposed to dark and light
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Differential gene expression in Alternaria gaisen exposed to dark andTI Differential gene expression in Alternaria gaisen exposed to dark and light

机译:暴露在黑暗和光明中的链格孢菌中的差异基因表达

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Character states during sporulation have been used to segregate and describe many small-spored species of Alternaria, but some are not supported by published phylogenetic analyses. The conidiation response of Alternaria gaisen was characterized by selective subtractive hybridization of cDNA produced from cultures of A. gaisen grown either in total darkness or in total darkness followed by scarification and 24 h exposure to light. Transcripts or their translation products were identified using BLAST. Multiple transcripts with similarity to ORF-1 of the AM-toxin gene were obtained from the light library. L152 is a full reading frame EST in the light library whose ORF translation has similarity to the conserved domain aegerolysin (pfam06355). A set of 11 ex-type or representative isolates including A. alternata, A. gaisen, A. yaliinficiens, A. arborescens, A. tenuissima and A. brassicicola were resolved by UPGMA analysis of a partial genomic sequence (415-425 base pairs) of L152, but were not resolved by a similar analysis of ITS sequences. Furthermore, the resolved lineages of the L152 dataset were reflective of the diversity previously hypothesized by morphological evaluations of sporulation patterns. Although the ITS rDNA sequence region is generally accepted as the most likely candidate for fungal barcoding, the analysis of L152 sequences presented here resolved closely related species or species groups where other loci, including ITS, have not. Based on these results, the sequences of putative aegerolysin homologs were variable, parsimony-informative and warrant additional analyses with a broader isolate set including related genera and species.
机译:孢子形成过程中的特征状态已被用来隔离和描述许多小链格孢属的物种,但是一些已发表的系统发育分析不支持这种状态。盖氏链格孢的分生孢子反应的特征在于选择性地减去杂交的cDNA,该cDNA是由在完全黑暗或完全黑暗中生长的盖氏假单胞菌培养物产生的,随后是划痕和暴露于光下24 h。使用BLAST鉴定转录本或其翻译产物。从光文库中获得了与AM毒素基因的ORF-1相似的多个转录本。 L152是光文库中的完整阅读框EST,其ORF翻译与保守域aegerolysin(pfam06355)相似。通过UPGMA对部分基因组序列(415-425个碱基对)的分析,分离出11种前型或代表性分离株,包括链格孢霉,盖氏拟南芥,yaliinficiens,侧柏拟南芥,tenuissima和芸苔霉。 ),但无法通过ITS序列的类似分析解决。此外,L152数据集的解析谱系反映了先前通过孢子形成形态的形态学评估所假设的多样性。尽管通常将ITS rDNA序列区域作为真菌条形码的最可能候选者,但此处介绍的L152序列分析可解析紧密相关的物种或物种组,而其他位点(包括ITS)则没有。根据这些结果,推定的aegerolysin同源物的序列是可变的,具有简约信息,并需要使用包括相关属和种在内的更广泛的分离物进行额外的分析。

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