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Identification of a group of Mus dunni endogenous virus-like endogenous retroviruses from the C57BL/6J mouse genome: proviral genomes strain distribution expression characteristics and genomic integration profile

机译:一组小家鼠的识别dunni内源性病毒样从C57BL / 6J小鼠基因组内源性逆转录病毒:原病毒基因组应变分布表达特征和基因组整合轮廓

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摘要

About 10 % of the mouse genome is occupied by sequences associated with endogenous retroviruses (ERVs). However, a comprehensive profile of the mouse ERVs and related elements has not been established yet. In this study, we identified a group of ERVs from the mouse genome and characterized their biological properties. Using a custom ERV mining protocol, 191 ERVs (159 loci reported previously and 32 new loci), tentatively named Mus dunni endogenous virus (MDEV)-like ERVs (MDL-ERVs), were mapped on the C57BL/6J mouse genome. Seven of them retained putative full coding potentials for three retroviral polypeptides (gag, pol, and env). Among the 57 mouse strains examined, all but the Mus pahari/Ei strain had PCR amplicons corresponding to a conserved MDL-ERV region. Interestingly, the Mus caroli/EiJ’s amplicon was somewhat larger than the others, coinciding with a substantial phylogenetic distance between the MDL-ERV populations of Mus caroli/EiJ and C57BL/6J strains. MDLERVs were highly expressed in the lung, spleen, and thymus of C57BL/6J mice compared to the brain, heart, kidney, and liver. Seven MDL-ERVs were mapped in the introns of six annotated genes. Of interest, some MDL-ERVs were mapped periodically on three clusters in the chromosome X. The finding that these MDL-ERVs were one of several types of retroelements, which form mosaic-repeat units of tandem arrays, suggests that the formation of the mosaicrepeat unit preceded the tandem arrangement event. Further studies are warranted to understand the biological roles of MDL-ERVs in both normal and pathologic conditions.
机译:与内源性逆转录病毒(ERV)相关的序列占据了大约10%的小鼠基因组。但是,尚未建立小鼠ERV和相关元素的全面概况。在这项研究中,我们从小鼠基因组中鉴定出一组ERV,并对其生物学特性进行了表征。使用定制的ERV挖掘协议,将191个ERV(先前报道的159个基因座和32个新基因座)(暂定名为Mus dunni内源病毒(MDEV)样ERV(MDL-ERV))定位在C57BL / 6J小鼠基因组上。其中七个保留了三个逆转录病毒多肽(gag,pol和env)的推定的完整编码潜能。在所检查的57个小鼠品系中,除Mus pahari / Ei品系以外的所有品系均具有对应于保守MDL-ERV区的PCR扩增子。有趣的是,Mus caroli / EiJ的扩增子稍大于其他扩增子,这与Mus caroli / EiJ的MDL-ERV种群和C57BL / 6J菌株之间的系统发育距离相符。与脑,心脏,肾脏和肝脏相比,MDLERV在C57BL / 6J小鼠的肺,脾和胸腺中高表达。在六个带注释基因的内含子中定位了七个MDL-ERV。有趣的是,一些MDL-ERV周期性地映射在X染色体上的三个簇上。这些MDL-ERV是几种类型的反转录元素之一,形成了串联阵列的镶嵌重复单元,这表明镶嵌重复的形成单元在串联安排事件之前。有必要进行进一步的研究来了解MDL-ERV在正常和病理状态下的生物学作用。

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