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利用来自长末端重复序列区域的寡核苷酸探针定位内源性非嗜亲性前病毒。

Endogenous nonecotropic proviruses mapped with oligonucleotide probes from the long terminal repeat region.

作者信息

Frankel W N, Coffin J M

机构信息

Jackson Laboratory, Bar Harbor, Maine 04609.

出版信息

Mamm Genome. 1994 May;5(5):275-81. doi: 10.1007/BF00389541.

Abstract

We characterized endogenous proviruses in C57BL/6J, DBA/2J, and C3H/HeJ mouse strains with oligonucleotide probes derived from long terminal repeat (LTR) sequences of three classes of nonecotropic murine leukemia virus. The segregation of proviral-host DNA junction fragments was followed in BXH and BXD recombinant inbred (RI) strain sets, and most fragments mapped readily to defined chromosomal regions. Most of the LTR fragments appear to correspond to proviruses mapped previously with oligonucleotide env region probes of the same viral class. At least 22 elements represent new proviral loci, no more than half of which may be solo LTRs, and an additional six may correspond to proviruses identified previously with less specific hybridization probes. Together with proviruses identified previously with env probes, the LTR probe-reactive elements represent the majority of endogenous murine leukemia proviruses in the mouse genome.

摘要

我们用源自三类非嗜亲性鼠白血病病毒长末端重复序列(LTR)的寡核苷酸探针,对C57BL/6J、DBA/2J和C3H/HeJ小鼠品系中的内源性前病毒进行了特征分析。在BXH和BXD重组近交(RI)品系组中追踪前病毒-宿主DNA连接片段的分离情况,大多数片段很容易定位到特定的染色体区域。大多数LTR片段似乎对应于先前用同一病毒类别的寡核苷酸env区域探针定位的前病毒。至少有22个元件代表新的前病毒位点,其中不超过一半可能是单独的LTR,另外六个可能对应于先前用特异性较低的杂交探针鉴定的前病毒。与先前用env探针鉴定的前病毒一起,LTR探针反应性元件代表了小鼠基因组中大多数内源性鼠白血病前病毒。

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