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Gene discovery and expression profiling in the toxin-producing marine diatom, Pseudo-nitzschia multiseries (Hasle) Hasle

机译:生成毒素的海洋硅藻,伪硝酸盐多重(Hasle)Hasle的基因发现和表达谱分析

摘要

Toxic algae are a growing concern in the marine environment. One unique marine diatom, Pseudo-nitzschia multiseries (Hasle) Hasle, produces the neurotoxin domoic acid, which is the cause of amnesic shellfish poisoning. The molecular characterization of this organism has been limited to date. Therefore, the focus of this thesis was to identify and initiate characterization of actively expressed genes that control cell growth and physiology in P. multiseries, with the specific goal of identifying genes that may play a significant role in toxin production. The first step in gene discovery was to establish a complementary DNA (cDNA) library and a database of expressed sequence tags (ESTs) for P. multiseries. 2552 cDNAs were sequenced, generating a set of 1955 unique contigs, of which 21% demonstrated significant similarity with known protein coding sequences. Among the genes identified by sequence similarity were several involved in photosynthetic pathways, including fucoxanthin-chlorophyll a/c light harvesting protein and a C4-specific pyruvate, orthophosphate dikinase. Several genes that may be involved in domoic acid synthesis were also revealed through sequence similarity, for example, glutamate dehydrogenase and 5-oxo-L-prolinase. In addition, the identification of sequences that appear novel to Pseudo-nitzschia may provide insight into unique aspects of Pseudo-nitzschia biology, such as toxin production. Genes whose expression patterns were correlated with toxin production were identified by hybridization to a microarray manufactured from 5376 cDNAs. 121 cDNAs, representing 12 unique cDNA contigs or non-redundant cDNAs, showed significantly increased expression levels in P. multiseries cell populations that were actively producing toxin.
机译:有毒藻类是海洋环境中日益引起关注的问题。一种独特的海洋硅藻,Pseudo-Nitzschia multiseries(Hasle)Hasle,产生神经毒素多摩酸,这是导致遗忘性贝类中毒的原因。迄今为止,该生物的分子表征还受到限制。因此,本论文的重点是鉴定并启动表征多基因疟原虫的控制细胞生长和生理的主动表达基因,其特定目的是鉴定可能在毒素产生中起重要作用的基因。基因发现的第一步是建立互补DNA(cDNA)文库和多序列疟原虫表达序列标签(EST)数据库。对2552个cDNA进行了测序,生成了1955个独特的重叠群,其中21%的片段与已知的蛋白质编码序列表现出显着的相似性。在通过序列相似性鉴定的基因中,有几个参与光合途径,包括岩藻黄质-叶绿素a / c收光蛋白和C4特异性丙酮酸,正磷酸二激酶。还通过序列相似性揭示了一些可能与多摩酸合成有关的基因,例如谷氨酸脱氢酶和5-氧代-L-脯氨酸酶。另外,鉴定对伪念珠菌新颖的序列可以提供对伪念珠菌生物学的独特方面的见解,例如毒素产生。通过与由5376个cDNA制造的微阵列杂交来鉴定其表达模式与毒素产生相关的基因。代表12个独特cDNA重叠群或非冗余cDNA的121个cDNA在正在积极产生毒素的P.多系列细胞群体中显示出明显升高的表达水平。

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