Lidie Kristy B, Ryan James C, Barbier Michele, Van Dolah Frances M
Marine Biotoxins Program, NOAA Center for Coastal Environmental and Biomolecular Research, SC 29412, USA.
Mar Biotechnol (NY). 2005 Sep-Oct;7(5):481-93. doi: 10.1007/s10126-004-4110-6.
Karenia brevis (Davis) is the dinoflagellate responsible for nearly annual red tides in the Gulf of Mexico. Although the mechanisms regulating the growth and toxicity of this problematic organism are of considerable interest, little information is available on its molecular biology. We therefore constructed a complementary DNA library from which to gain insight into its expressed genome and to develop tools for studying its gene expression. Large-scale sequencing yielded 7001 high-quality expressed sequence tags (ESTs), which clustered into 5280 unique gene groups. The vast majority of genes expressed fell into a low-abundance class, with the highest expressed gene accounting for only 1% of the total ESTs. Approximately 29% of genes were found to have similarity to known sequences in other organisms after BLAST similarity comparisons to the GenBank public protein database using a cutoff of P < 10e(-4). We identified for the first time in a dinoflagellate a suite of conserved eukaryotic genes involved in cell cycle control, intracellular signaling, and the transcription and translation machinery. At least 40% of gene clusters displayed single nucleotide polymorphisms, suggesting the presence of multiple gene copies. The average GC content of ESTs was 51%, with a slight preference for G or C in the third codon position (53.5%). The ESTs were used to develop an oligonucleotide microarray containing 4629 unique features and 3462 replicate probes. Microarray labeling has been optimized, and the microarray has been validated for probe specificity and reproducibility. This is the first information to be developed on the expressed genome of K. brevis and provides the basis from which to begin functional genomic studies on this harmful algal bloom species.
短裸甲藻(Davis)是导致墨西哥湾几乎每年都会出现赤潮的甲藻。尽管调节这种有问题生物的生长和毒性的机制备受关注,但其分子生物学方面的信息却很少。因此,我们构建了一个互补DNA文库,以深入了解其表达基因组,并开发研究其基因表达的工具。大规模测序产生了7001个高质量的表达序列标签(EST),这些标签聚集成5280个独特的基因组。绝大多数表达的基因属于低丰度类别,表达量最高的基因仅占总EST的1%。在使用P < 10e(-4)的阈值与GenBank公共蛋白质数据库进行BLAST相似性比较后,发现约29%的基因与其他生物中的已知序列具有相似性。我们首次在甲藻中鉴定出一组参与细胞周期控制、细胞内信号传导以及转录和翻译机制的保守真核基因。至少40%的基因簇显示出单核苷酸多态性,表明存在多个基因拷贝。EST的平均GC含量为51%,在第三个密码子位置对G或C略有偏好(53.5%)。这些EST被用于开发一个包含4629个独特特征和3462个重复探针的寡核苷酸微阵列。微阵列标记已得到优化,并且该微阵列已针对探针特异性和可重复性进行了验证。这是关于短裸甲藻表达基因组的首个信息,为开始对这种有害藻华物种进行功能基因组学研究提供了基础。