Ellis J T, Amoyal G, Ryce C, Harper P A, Clough K A, Homan W L, Brindley P J
Department of Cell & Molecular Biology, University of Technology, Sydney, Australia.
Mol Cell Probes. 1998 Feb;12(1):1-13. doi: 10.1006/mcpr.1997.0143.
The latest release of the large subunit ribosomal database contains 429 sequences, yet only 10 (six nuclear and four mitochondrial) are derived from parasites of the phylum Apicomplexa. Three of these (all Toxoplasma gondii) were previously contained in the 1994 release of the database. As an initiative towards an understanding of ribosomal gene organization in the Apicomplexa, the primary sequence of the large subunit (LSU) rDNA of Neospora caninum is presented, and compared with a consensus sequence derived for the LSU rDNA of T. gondii. Nucleotide differences observed between these two taxa in the D2 expansion segment (or domain) (also called the C1/C1' region) of the LSU rDNA were incorporated into a primer that forms the basis of a species-specific polymerase chain reaction (PCR) for N. caninum. The D2 domain of the LSU rDNA, therefore, represents a new genetic marker that can be used for the differentiation and identification of Neospora from other cyst-forming coccidia.
最新版的大亚基核糖体数据库包含429条序列,但其中只有10条(6条来自细胞核,4条来自线粒体)来自顶复门寄生虫。其中3条(均为刚地弓形虫)先前包含在1994年发布的数据库中。为了深入了解顶复门中的核糖体基因组织,本文给出了犬新孢子虫大亚基(LSU)rDNA的一级序列,并与从刚地弓形虫LSU rDNA推导得到的共有序列进行了比较。在LSU rDNA的D2扩展片段(或结构域)(也称为C1/C1'区域)中观察到的这两个分类单元之间的核苷酸差异被纳入到一个引物中,该引物构成了犬新孢子虫物种特异性聚合酶链反应(PCR)的基础。因此,LSU rDNA的D2结构域代表了一种新的遗传标记,可用于将新孢子虫与其他形成包囊的球虫进行区分和鉴定。