Rios Jonathan J, Perelygin Andrey A, Long Maureen T, Lear Teri L, Zharkikh Andrey A, Brinton Margo A, Adelson David L
Department of Animal Science, Texas A&M University, 2471 TAMU, College Station, Texas 77843, USA.
BMC Genomics. 2007 Sep 7;8:313. doi: 10.1186/1471-2164-8-313.
The mammalian OAS/RNASEL pathway plays an important role in antiviral host defense. A premature stop-codon within the murine Oas1b gene results in the increased susceptibility of mice to a number of flaviviruses, including West Nile virus (WNV). Mutations in either the OAS1 or RNASEL genes may also modulate the outcome of WNV-induced disease or other viral infections in horses. Polymorphisms in the human OAS gene cluster have been previously utilized for case-control analysis of virus-induced disease in humans. No polymorphisms have yet been identified in either the equine OAS1 or RNASEL genes for use in similar case-control studies.
Genomic sequence for equine OAS1 was obtained from a contig assembly generated from a shotgun subclone library of CHORI-241 BAC 100I10. Specific amplification of regions of the OAS1 gene from 13 horses of various breeds identified 33 single nucleotide polymorphisms (SNP) and two microsatellites. RNASEL cDNA sequences were determined for 8 mammals and utilized in a phylogenetic analysis. The chromosomal location of the RNASEL gene was assigned by FISH to ECA5p17-p16 using two selected CHORI-241 BAC clones. The horse genomic RNASEL sequence was assembled. Specific amplification of regions of the RNASEL gene from 13 horses identified 31 SNPs.
In this report, two dinucleotide microsatellites and 64 single nucleotide polymorphisms within the equine OAS1 and RNASEL genes were identified. These polymorphisms are the first to be reported for these genes and will facilitate future case-control studies of horse susceptibility to infectious diseases.
哺乳动物的OAS/RNASEL通路在抗病毒宿主防御中起重要作用。小鼠Oas1b基因内的一个提前终止密码子导致小鼠对包括西尼罗河病毒(WNV)在内的多种黄病毒易感性增加。OAS1或RNASEL基因的突变也可能调节WNV诱导疾病或马的其他病毒感染的结果。人类OAS基因簇中的多态性先前已用于人类病毒诱导疾病的病例对照分析。尚未在马的OAS1或RNASEL基因中鉴定出用于类似病例对照研究的多态性。
马OAS1的基因组序列是从由CHORI-241 BAC 100I10的鸟枪法亚克隆文库生成的重叠群组装中获得的。从13匹不同品种的马中对OAS1基因区域进行特异性扩增,鉴定出33个单核苷酸多态性(SNP)和两个微卫星。测定了8种哺乳动物的RNASEL cDNA序列并用于系统发育分析。使用两个选定的CHORI-241 BAC克隆通过荧光原位杂交(FISH)将RNASEL基因的染色体定位到ECA5p17-p16。组装了马基因组RNASEL序列。从13匹马中对RNASEL基因区域进行特异性扩增,鉴定出31个SNP。
在本报告中,鉴定出马OAS1和RNASEL基因内的两个二核苷酸微卫星和64个单核苷酸多态性。这些多态性是这些基因首次被报道,将有助于未来关于马对传染病易感性的病例对照研究。