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原鸡和白来航鸡ESTs中序列多态性的检测。

Detection of sequence polymorphisms in red junglefowl and White Leghorn ESTs.

作者信息

Fitzsimmons C J, Savolainen P, Amini B, Hjälm G, Lundeberg J, Andersson L

机构信息

Department of Medical Biochemistry and Microbiology, Uppsala University, SE-751 24, Sweden.

出版信息

Anim Genet. 2004 Oct;35(5):391-6. doi: 10.1111/j.1365-2052.2004.01184.x.

Abstract

Over 16,000 high quality expressed sequence tags (ESTs) from red junglefowl (RJ) and White Leghorn (WL) brain and testis cDNA libraries were generated. Here, we have used this resource for detection of single nucleotide polymorphisms (SNPs), and also completed full-length sequencing of 46 pairs of clones, representing the same gene from both the RJ and WL libraries. From the main set of ESTs, which were assembled using Phrap, 746 putative SNPs were identified, of which 76% were transitions and 24% were transversions. A subset of SNPs was evaluated by sequence analysis of five RJ and five WL birds. Nine of 12 SNPs were verified in this limited sample, suggesting that a majority of the putative polymorphisms documented in this study represent real SNPs. During full-length sequencing of the 46 RJ/WL clones 100 SNPs were identified, which translated to a frequency of 1.90 SNPs/1000 bp. The number of transitions and transversions were 77% and 23%, respectively, and the proportion of non-synonymous vs. synonymous SNPs was 20% and 80%, respectively. Four large insertions/deletions were identified between the RJ and WL full-length sequences, and they appear to represent different splice variants.

摘要

我们生成了来自红原鸡(RJ)和白来航鸡(WL)大脑及睾丸cDNA文库的16000多个高质量表达序列标签(EST)。在此,我们利用这些资源检测单核苷酸多态性(SNP),并完成了46对克隆的全长测序,这些克隆代表了RJ文库和WL文库中的同一基因。在使用Phrap组装的主要EST集合中,鉴定出746个推定的SNP,其中76%为转换,24%为颠换。通过对5只RJ鸡和5只WL鸡的序列分析评估了一部分SNP。在这个有限的样本中,12个SNP中有9个得到了验证,这表明本研究中记录的大多数推定多态性代表真实的SNP。在对46个RJ/WL克隆进行全长测序的过程中,鉴定出100个SNP,转换为频率为1.90个SNP/1000 bp。转换和颠换的数量分别为77%和23%,非同义SNP与同义SNP的比例分别为20%和80%。在RJ和WL的全长序列之间鉴定出4个大的插入/缺失,它们似乎代表不同的剪接变体。

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