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物种、序列类型和等位基因:剖析……中的遗传变异

Species, Sequence Types and Alleles: Dissecting Genetic Variation in .

作者信息

Fuerst Paul A, Booton Gregory C

机构信息

Department of Evolution, Ecology and Organismal Biology, The Ohio State University, Columbus, OH 43210, USA.

Department of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA.

出版信息

Pathogens. 2020 Jul 2;9(7):534. doi: 10.3390/pathogens9070534.

Abstract

Species designations within are problematic because of pleomorphic morphology. Molecular approaches, including DNA sequencing, hinted at a resolution that has yet to be fully achieved. Alternative approaches were required. In 1996, the Byers/Fuerst lab introduced the concept of sequence types. Differences between isolates of could be quantitatively assessed by comparing sequences of the nuclear 18S rRNA gene, ultimately producing 22 sequence types, designated T1 through T22. The concept of sequence types helps our understanding of evolution. Nevertheless, substantial variation in the 18S rRNA gene differentiates many isolates within each sequence type. Because the majority of isolates with sequences in the international DNA databases have been studied for only a small segment of the gene, designated ASA.S1, genetic variation within this hypervariable region of the 18S rRNA gene has been scrutinized. In 2002, we first categorized variation in this region in a sample of T3 and T4 isolates from Hong Kong, observing ten "alleles" within type T4 and five "alleles" within T3. Subsequently, confusion occurred when different labs applied redundant numerical labels to identify different alleles. A more unified approach was required. We have tabulated alleles occurring in the sequences submitted to the international DNA databases, and determined their frequencies. Over 150 alleles have occurred more than once within 3500+ isolates of sequence type T4. Results from smaller samples of other sequence types (T3, T5, T11 and T15, and supergroup T2/6) have also been obtained. Our results provide new insights into the evolutionary history of , further illuminating the degree of genetic separation between significant taxonomic units within the genus, perhaps eventually elucidating what constitutes a species of .

摘要

由于其多形性形态,[该物种名称]内的物种命名存在问题。包括DNA测序在内的分子方法暗示了一种尚未完全实现的分辨率。需要其他方法。1996年,拜尔斯/富尔斯特实验室引入了序列类型的概念。通过比较核18S rRNA基因的序列,可以定量评估[该物种]分离株之间的差异,最终产生22种序列类型,命名为T1至T22。序列类型的概念有助于我们理解[该物种]的进化。然而,18S rRNA基因的大量变异使每个序列类型中的许多分离株有所不同。由于国际DNA数据库中大多数具有序列的分离株仅针对该基因的一小段(命名为ASA.S1)进行了研究,因此对18S rRNA基因这个高变区域内的遗传变异进行了仔细审查。2002年,我们首次对来自香港的T3和T4分离株样本中该区域的变异进行了分类,在T4类型中观察到10个“等位基因”,在T3类型中观察到5个“等位基因”。随后,当不同实验室使用冗余数字标签来识别不同等位基因时出现了混淆。需要一种更统一的方法。我们已将提交到国际DNA数据库的序列中出现的等位基因制成表格,并确定了它们的频率。在3500多个序列类型T4的分离株中,有150多个等位基因出现不止一次。也获得了其他序列类型(T3、T5、T11和T15以及超群T2/6)较小样本的结果。我们的结果为[该物种]的进化历史提供了新的见解,进一步阐明了该属内重要分类单元之间的遗传分离程度,也许最终能阐明什么构成了[该物种]的一个物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed91/7400246/850b909c55b0/pathogens-09-00534-g001.jpg

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