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Novel polymorphisms in the Cryptosporidium hominis genome

机译:隐孢子虫Hominis基因组中的新型多态性

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The purpose of this study was to compare genomic sequences of oocysts derived from sporadic human cryptosporidiosis cases in Canada to the published genomic sequence of Cryptosporidium hominis at select gene loci distributed over several chromosomes. A total of 46 loci on 7 chromosomes were analyzed. Sequence polymorphisms were found at 50 positions on 22 loci in 20 different contigs. While some of these polymorphisms included synonymous single nucleotide polymorphisms (SNPs), many were non-synonymous (NS) and the largest variations included a locus with a 120bp deletion on chromosome (Chr) 7 and a locus with a 90bp insertion on Chr 3. Of the sequence variations found, 39 resulted in amino acid substitutions in the predicted protein sequences with the large insertion coding for a glutamine(Q)-rich pentameric repeat region. The results from this study showed that approximately half the loci sequenced were variant from the reported genomic sequence of the TU502 isolate from Uganda.
机译:本研究的目的是将卵囊的基因组序列与加拿大源自染色体的Pryptosperidium Hominis的发表的基因组序列进行比较,分布在几种染色体上。 分析了7个染色体上的46个基因座。 在20种不同的聚体中,在22个基因座的50个位置发现序列多态性。 虽然这些多态性中的一些包括同义的单一核苷酸多态性(SNP),但是许多是非同义(NS),并且最大的变化包括在染色体(CHR)7上具有120bp缺失的基因座,并且在CHR 3上插入90bp插入的基因座。 发现的序列变异,39导致预测蛋白质序列中的氨基酸取代具有大的插入谷氨酰胺(Q) - 中等戊酰胺重复区域。 本研究的结果表明,从乌干达的报告的TU502分离液的报告的基因组序列中大约一半的基因座测序。

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