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检测越南本土猪基因组中的非参考猪内源性逆转录病毒基因座。

Detection of non-reference porcine endogenous retrovirus loci in the Vietnamese native pig genome.

机构信息

Institute of Agrobiological Sciences, National Agriculture and Food Research Organization, Owashi 1-2, Tsukuba, Ibaraki, 305-8634, Japan.

Department of Animal Science, Nippon Veterinary and Life Science University, 1-7-1 Kyonancho, Musashino, Tokyo, Japan, 180-8602.

出版信息

Sci Rep. 2022 Jun 21;12(1):10485. doi: 10.1038/s41598-022-14654-4.

Abstract

The Vietnamese native pig (VnP)-a porcine breed with a small body-has proven suitable as a biomedical animal model. Here, we demonstrate that, compared to other breeds, VnPs have fewer copies of porcine endogenous retroviruses (PERVs), which pose a risk for xenotransplantation of pig organs to humans. More specifically, we sought to characterize non-reference PERVs (nrPERVs) that were previously unidentified in the reference genome. To this end, we used whole-genome sequencing data to identify nrPERV loci with long terminal repeat (LTR) sequences in VnPs. RetroSeq was used to estimate nrPERV loci based on the most current porcine reference genome (Sscrofa11.1). LTRs were detected using de novo sequencing read assembly near the loci containing the target site duplication sequences in the inferred regions. A total of 21 non-reference LTR loci were identified and separated into two subtypes based on phylogenetic analysis. Moreover, PERVs within the detected LTR loci were identified, the presence of which was confirmed using conventional PCR and Sanger sequencing. These novel loci represent previously unknown PERVs as they have not been identified in the porcine reference genome. Thus, our RetroSeq method accurately detects novel PERV loci, and can be applied for development of a useful biomedical model.

摘要

越南本地猪(VnP)是一种体型较小的猪种,已被证明适合作为生物医学动物模型。在这里,我们证明与其他品种相比,VnP 中猪内源性逆转录病毒(PERV)的拷贝数较少,这降低了猪器官异种移植到人类的风险。更具体地说,我们试图对先前在参考基因组中未被识别的非参考 PERV(nrPERV)进行特征描述。为此,我们使用全基因组测序数据来鉴定 VnP 中具有长末端重复(LTR)序列的 nrPERV 基因座。RetroSeq 用于根据最新的猪参考基因组(Sscrofa11.1)来估算 nrPERV 基因座。使用从头测序读取组装来检测 LTR,这些读取组装在推断区域中包含靶序列重复序列的基因座附近进行。总共鉴定出 21 个非参考 LTR 基因座,并根据系统发育分析将其分为两种亚型。此外,还鉴定了在所检测的 LTR 基因座内的 PERV,使用常规 PCR 和 Sanger 测序确认了它们的存在。这些新的基因座代表了以前未知的 PERV,因为它们在猪参考基因组中未被识别。因此,我们的 RetroSeq 方法可以准确检测新的 PERV 基因座,并可用于开发有用的生物医学模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b0b/9213404/70f2c3069024/41598_2022_14654_Fig1_HTML.jpg

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