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带有鼠类序列的 DNA 提取柱污染。

DNA extraction columns contaminated with murine sequences.

机构信息

Jefferiss Research Trust Laboratories, Section of Infectious Diseases, Imperial College London, London, United Kingdom.

出版信息

PLoS One. 2011;6(8):e23484. doi: 10.1371/journal.pone.0023484. Epub 2011 Aug 18.

Abstract

Sequences of the novel gammaretrovirus, xenotropic murine leukemia virus-related virus (XMRV) have been described in human prostate cancer tissue, although the amounts of DNA are low. Furthermore, XMRV sequences and polytropic (p) murine leukemia viruses (MLVs) have been reported in patients with chronic fatigue syndrome (CFS). In assessing the prevalence of XMRV in prostate cancer tissue samples we discovered that eluates from naïve DNA purification columns, when subjected to PCR with primers designed to detect genomic mouse DNA contamination, occasionally gave rise to amplification products. Further PCR analysis, using primers to detect XMRV, revealed sequences derived from XMRV and pMLVs from mouse and human DNA and DNA of unspecified origin. Thus, DNA purification columns can present problems when used to detect minute amounts of DNA targets by highly sensitive amplification techniques.

摘要

新型γ逆转录病毒、嗜性小鼠白血病病毒相关病毒(XMRV)的序列已在人类前列腺癌组织中描述,尽管 DNA 数量很低。此外,XMRV 序列和多嗜性(p)小鼠白血病病毒(MLV)已在慢性疲劳综合征(CFS)患者中报道。在评估 XMRV 在前列腺癌组织样本中的流行率时,我们发现,当用设计用于检测基因组小鼠 DNA 污染的引物进行 PCR 时,来自天真 DNA 纯化柱的洗脱液偶尔会产生扩增产物。进一步的 PCR 分析,使用检测 XMRV 的引物,揭示了源自 XMRV 和 pMLV 的序列,以及来自小鼠和人 DNA 以及未指定来源的 DNA。因此,当使用高度敏感的扩增技术检测微量 DNA 靶标时,DNA 纯化柱会出现问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc9/3158089/254c6945e0ad/pone.0023484.g001.jpg

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