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从硬壳蛤 Meretrix meretrix 的 ESTs 中鉴定宿主防御基因和开发微卫星标记。

Identification of host-defense genes and development of microsatellite markers from ESTs of hard clam Meretrix meretrix.

机构信息

Liaoning Key Laboratory of Marine Fishery Molecular Biology, Liaoning Ocean and Fishery Science Institute, Dalian, 116023, China.

出版信息

Mol Biol Rep. 2011 Feb;38(2):769-75. doi: 10.1007/s11033-010-0165-4. Epub 2010 Apr 8.

Abstract

The hard clam Meretrix meretrix is an economically important shellfish in China. However, genomic research on this species is still at early stage, and few genomic resources are available. The objective of the present study was to generate expressed sequence tags (ESTs), and identify host-defense genes and microsatellite markers for M. meretrix. Three cDNA libraries for intestine, mantle and hepatopancreas were constructed using highly efficient SMART (Switching Mechanism At 5' end of the RNA Transcript) method. A total of 3224 random clones were single-pass sequenced from 5'-ends, resulting in 3129 high-quality (>100 bp) ESTs averaging 734 bp. All the ESTs were assembled by software Cap 3, producing 1796 unigenes-1490 singletons and 306 contigs. All the unigenes were compared to the public protein database using tblastx, and 696 (38.8%) were homologues to known genes while the remaining 1100 (61.2%) appeared to be novel sequences. A total of 31 EST clusters were related to immune and defense functions. They included immune recognition receptors, proteases and protease inhibitors, and other immune-related genes. The screening of 1796 unigenes identified 55 (3.1%) microsatellite-containing sequences, with 20 having sufficient flanking sequences for primer design. Polymerase chain reaction amplification was successful for 12 primer pairs and 7 of them showed polymorphic. The EST collection and microsatellite markers obtained in this study provide a useful resource for further gene discovery and population genetic analysis in M. meretrix.

摘要

中国的文蛤 Meretrix meretrix 是一种具有重要经济价值的贝类。然而,该物种的基因组研究仍处于早期阶段,可用的基因组资源有限。本研究的目的是生成表达序列标签(EST),并鉴定文蛤的宿主防御基因和微卫星标记。使用高效的 SMART(RNA 转录物 5'端的转换机制)方法构建了肠、套膜和肝胰腺三个 cDNA 文库。从 5'-末端对 3224 个随机克隆进行了单端测序,得到了 3129 条高质量(>100 bp)的 EST,平均长度为 734 bp。所有 EST 均由软件 Cap 3 组装,产生了 1796 个非重叠基因-1490 个单基因和 306 个基因簇。所有的非重叠基因都使用 tblastx 与公共蛋白质数据库进行了比较,其中 696 个(38.8%)与已知基因同源,而其余 1100 个(61.2%)似乎是新的序列。共有 31 个 EST 簇与免疫和防御功能有关。它们包括免疫识别受体、蛋白酶和蛋白酶抑制剂以及其他免疫相关基因。对 1796 个非重叠基因的筛选发现了 55 个(3.1%)含有微卫星的序列,其中 20 个具有足够的侧翼序列用于引物设计。12 对引物的聚合酶链反应扩增成功,其中 7 对具有多态性。本研究获得的 EST 集和微卫星标记为进一步研究文蛤的基因发现和群体遗传分析提供了有用的资源。

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