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首页> 外文期刊>Journal of Virology >Characterization of Rous sarcoma virus-related sequences in the Japanese quail.
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Characterization of Rous sarcoma virus-related sequences in the Japanese quail.

机译:日本鹌鹑中肉瘤病毒相关序列的表征。

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摘要

We detected sequences related to the avian retrovirus Rous sarcoma virus within the genome of the Japanese quail, a species previously considered to be free of endogenous avian leukosis virus elements. Using low-stringency conditions of hybridization, we screened a quail genomic library for clones containing retrovirus-related information. Of five clones so selected, one, lambda Q48, contained sequence information related to the gag, pol, and env genes of Rous sarcoma virus arranged in a contiguous fashion and spanning a distance of approximately 5.8 kilobases. This organization is consistent with the presence of an endogenous retroviral element within the Japanese quail genome. Use of this element as a high-stringency probe on Southern blots of genomic digests of several quail DNA demonstrated hybridization to a series of high-molecular-weight bands. By slot hybridization to quail DNA with a cloned probe, it was deduced that there were approximately 300 copies per diploid cell. In addition, the quail element also hybridized at low stringency to the DNA of the White Leghorn chicken and at high stringency to the DNAs of several species of jungle fowl and both true and ruffed pheasants. Limited nucleotide sequencing analysis of lambda Q48 revealed homologies of 65, 52, and 46% compared with the sequence of Rous sarcoma virus strain Prague C for the endonuclease domain of pol, the pol-env junction, and the 3'-terminal region of env, respectively. Comparisons at the amino acid level were also significant, thus confirming the retrovirus relatedness of the cloned quail element.
机译:我们检测到与日本鹌鹑的基因组内与禽逆转录病毒的肉瘤病毒有关的序列,以前被认为是没有内源性禽的白血病病毒元素的物种。使用杂交的低严格条件,我们筛选了含有逆转录病毒相关信息的克隆的鹌鹑基因组文库。其中五个克隆如此选择,一个,lambda Q48,包含与邻象时装的GAG,Pol和env基因相关的序列信息,并跨越大约5.8千碱基的距离。该组织与日本鹌鹑基因组内的内源性逆转录病毒元素一致。在几个鹌鹑DNA的基因组消化中使用该元素作为高度严格探针,证明了一系列高分子重量带的杂交。通过槽杂交以克隆探针鹌鹑DNA,推导出每分包电池约300份。此外,鹌鹑元素在白色leghorn鸡的DNA和高度严格的丛生中杂交地杂交,以及几种丛林家禽的DNA,以及真实和繁琐的野鸡。 Lambda Q48的有限核苷酸测序分析揭示了65,52和46%的同源物与Pol,Pol-Env结和env的3'-末端区域的内切核酸酶域的血清酶菌株Prague C的序列相比, 分别。氨基酸水平的比较也显着,因此证实了克隆鹌鹑元件的逆转录病毒相关性。

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