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内源性鼠白血病前病毒的连锁图谱。

A linkage map of endogenous murine leukemia proviruses.

作者信息

Frankel W N, Stoye J P, Taylor B A, Coffin J M

机构信息

Department of Molecular Biology, Tufts University School of Medicine, Boston, Massachusetts 02111.

出版信息

Genetics. 1990 Feb;124(2):221-36. doi: 10.1093/genetics/124.2.221.

Abstract

Thirty endogenous proviruses belonging to the modified polytropic (Mpmv) class of murine leukemia virus (MLV) were identified by proviral-cellular DNA junction fragment segregation in several sets of recombinant inbred mice. Twenty-six Mpmv loci were mapped to chromosomal regions by matching proviral strain distribution patterns to those of previously assigned genes. Like other endogenous nonecotropic MLVs, Mpmv loci were present on several chromosomes in all strains examined. We pooled recombinant inbred strain linkage data from 110 MLV loci and selected marker genes in order to construct a chromosomal linkage map. Every mouse chromosome was found to harbor at least one proviral insertion, and several regions contained multiple integrations. However, the overall distribution of the 110 mapped proviruses did not deviate significantly from a random distribution. Because of their polymorphism in inbred strains of mice, and the ability to score as many as 57 proviruses per strain using only three hybridization probes, the nonecotropic MLVs mapped in common strains of mice offer a significant advantage over older methods (e.g., biochemical or individual restriction fragment polymorphisms) as genetic markers. These endogenous insertion elements should also be useful for assessing strain purity, and for studying the relatedness of common and not-so-common inbred strains.

摘要

通过在几组重组近交系小鼠中进行前病毒 - 细胞DNA连接片段分离,鉴定出30种属于小鼠白血病病毒(MLV)修饰多嗜性(Mpmv)类别的内源性前病毒。通过将前病毒株分布模式与先前指定基因的模式相匹配,将26个Mpmv基因座定位到染色体区域。与其他内源性非亲嗜性MLV一样,在所检查的所有品系中,Mpmv基因座存在于几条染色体上。我们汇总了来自110个MLV基因座和选定标记基因的重组近交系连锁数据,以构建染色体连锁图谱。发现每条小鼠染色体至少含有一个前病毒插入,并且几个区域包含多个整合。然而,110个定位前病毒的总体分布与随机分布没有显著偏差。由于它们在小鼠近交系中的多态性,并且仅使用三个杂交探针就能对每个品系多达57个前病毒进行评分,因此在小鼠常见品系中定位的非亲嗜性MLV作为遗传标记比旧方法(例如生化或个体限制性片段多态性)具有显著优势。这些内源性插入元件也应该有助于评估品系纯度,以及研究常见和不太常见近交系的相关性。

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