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Construction and characterization of EST libraries from the porcelain crab, Petrolisthes cinctipes

机译:瓷蟹(Petrolisthes cinctipes)的EST库的构建和鉴定

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The thermal phenotype of an organism (heat and cold tolerance, thermal range, and thermal plasticity) is an essential feature of how the organism performs across thermal environments and in response to thermal stress. Porcelain crabs are of interest in addressing questions of thermal phenotype because of their high species diversity and the large variation in thermal phenotype among species, as well as the biogeographic patterning of these crabs along environmental stress gradients. We are studying the cellular bases of thermal phenotype and physiological responses to environmental stress using a functional genomics cDNA microarray approach. To do this, we have isolated total RNA from a range of tissues from 1 species of porcelain crab (Petrolisthes cinctipes) exposed to a suite of thermal conditions, and have used this RNA to construct a 13 824-clone EST library. Here, we describe construction, EST sequencing, assembly and clustering, and results of BLASTx homology search for our initial 13 824-clone library. From 12 060 usable ESTs, 6717 consensus sequences were identified, and roughly 50% of these have homology to known proteins. At present, an additional 50 000–75 000-clone library of P. cinctipes ESTs is being generated, with the aim of developing a library with near-complete coverage of the transcriptome. The libraries and sequence information that will be generated as a result of this project should be of value for crustacean biologists working across a broad range of scientific disciplines (for example, physiology, developmental biology, biological rhythms, ecology, fisheries biology), as well as in studies of molecular evolution and phylogeography.
机译:生物体的热表型(耐热和耐寒性,热范围和热可塑性)是生物体在整个热环境中以及如何响应热应激的重要特征。瓷蟹在解决热表型问题方面很受关注,因为它们具有较高的物种多样性和物种间热表型的巨大差异,以及这些螃蟹沿环境应力梯度的生物地理图案。我们正在研究使用功能基因组学cDNA微阵列方法的热表型和对环境压力的生理反应的细胞基础。为此,我们从暴露于一系列高温条件下的1种瓷蟹(Petrolisthes cinctipes)的一系列组织中分离了总RNA,并使用该RNA构建了13 824个克隆的EST文库。在这里,我们描述了我们最初的13 824个克隆文库的构建,EST测序,组装和聚类以及BLASTx同源性搜索的结果。从12 060个可用EST中,鉴定出6717个共有序列,其中大约50%与已知蛋白质具有同源性。目前,正在建立另外一个5万至7.5万个C.tips ESTs克隆的文库,目的是开发一个几乎完全覆盖转录组的文库。该项目的结果将产生的文库和序列信息对于在广泛的科学学科(例如,生理学,发育生物学,生物学节律,生态学,渔业生物学)中工作的甲壳类生物学家也具有价值。如分子进化和系统地理学的研究。

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