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首页> 外文期刊>Parasitology Research >Analysis of differentially expressed genes in the precocious line of Eimeria maxima and its parent strain using suppression subtractive hybridization and cDNA microarrays
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Analysis of differentially expressed genes in the precocious line of Eimeria maxima and its parent strain using suppression subtractive hybridization and cDNA microarrays

机译:利用抑制消减杂交和cDNA芯片分析大艾美耳虫及其亲本早熟系中差异表达的基因

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摘要

The precocious line of Eimeria spp., obtained by repeated passages of oocysts initially collected from feces of previously infected chickens, has unique phenotypes and plays an important role in immunizing chickens against coccidiosis. However, the genetic basis of precocious phenotype in Eimeria is still poorly understood. To investigate gene expression changes in sporulated oocysts between the precocious line of E. maxima and its parent strain, subtractive cDNA libraries were constructed by suppression subtractive hybridization (SSH). A total of 3,164 cDNA fragments were selected from the SSH cDNA libraries to fabricate cDNA microarrays and further identify the differentially expressed genes. The credibility of the microarray data was verified by real-time PCR. A total of 360 valid expressed sequence tags (ESTs) were obtained, which represented 32 unique sequences. Twenty-one genes were validated as downregulated and 11 genes as upregulated in the precocious line. Homology searching of the public sequence database showed that six genes encoded proteins homologous with previously reported proteins, including rhomboid-like protein and transhydrogenase of E. tenella, serpin, and cation-transporting ATPase of E. acervulina, a heat-shock protein of E. maxima, and a conserved hypothetical protein of Toxoplasma gondii. Thus, the remaining 26 ESTs have not been previously reported. Further characterization of these differentially expressed genes will be useful in understanding the genetic basis for the precocious phenotype in Eimeria spp.
机译:通过反复传代最初从先前感染过的鸡粪便中收集的卵囊获得的艾美球虫早熟系具有独特的表型,并在免疫鸡抗球虫病中起重要作用。但是,对艾美球虫早熟表型的遗传基础仍然知之甚少。为了研究大肠埃希氏菌的早熟线与其亲本菌株之间的孢子卵囊中的基因表达变化,通过抑制消减杂交(SSH)构建了消减cDNA文库。从SSH cDNA文库中总共选择了3,164个cDNA片段,以制造cDNA微阵列并进一步鉴定差异表达的基因。通过实时PCR验证了微阵列数据的可信度。总共获得了360个有效的表达序列标签(EST),它们代表了32个独特序列。早熟品系中有21个基因被确认为下调,有11个基因被确认为上调。对公共序列数据库的同源性搜索显示,六个基因编码的蛋白与以前报道的蛋白同源,包括菱形样蛋白和大肠杆菌的转氢酶,丝氨酸蛋白酶抑制剂,以及大肠杆菌的热激蛋白阳离子小球藻的阳离子转运ATPase。 ,以及弓形虫的保守假设蛋白。因此,剩余的26个EST以前没有报告过。这些差异表达的基因的进一步表征将有助于理解艾美球虫早熟表型的遗传基础。

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