首页> 外文期刊>Molecular and Cellular Biology >Dilute-coat-color locus of mice: nucleotide sequence analysis of the d+2J and d+Ha revertant alleles.
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Dilute-coat-color locus of mice: nucleotide sequence analysis of the d+2J and d+Ha revertant alleles.

机译:小鼠的稀外套色基因座:d + 2J和d + Ha回复等位基因的核苷酸序列分析。

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The unstable dilute-coat-color mutation (d) of DBA/2J mice has been shown to be the result of integration of an ecotropic murine leukemia virus within the mouse genome. Molecular cloning and restriction enzyme analysis of the dilute allele and the viral preintegration site (+ allele), as well as two independent dilute revertants (d+2J and d+Ha), suggested that reversion is due to virus excision occurring by homologous recombination involving the viral long terminal repeats. The DNA sequence has now been determined for the cell-virus junctions of the provirus associated with the d mutation, for the viral preintegration site, and for the two revertant sites. These data (i) indicate that the d mutation was caused by a normal virus integration, (ii) confirm that virus excision occurs by precise homologous recombination, as exactly one long terminal repeat is present in each revertant site, and (iii) suggest that the virus induced the d mutation by integration into a noncoding sequence.
机译:业已证明,DBA / 2J小鼠的不稳定的稀薄外套颜色突变(d)是在小鼠基因组中整合了嗜性鼠白血病病毒的结果。对稀等位基因和病毒预整合位点(+等位基因)以及两个独立的稀化回复子(d + 2J和d + Ha)的分子克隆和限制性内切酶分析表明,回复是由于同源重组引起的病毒切除而引起的。病毒的长末端重复出现。现在已经确定了与d突变相关的前病毒的细胞-病毒连接,病毒预整合位点和两个回复位点的DNA序列。这些数据(i)表明d突变是由正常的病毒整合引起的;(ii)确认病毒的切除是通过精确的同源重组发生的,因为每个回复位点中均存在一个长末端重复序列,并且(iii)表明该病毒通过整合到非编码序列中诱导了d突变。

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