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种间回交为小鼠染色体的着丝粒作图提供了一种重要的新工具。

Interspecific backcrosses provide an important new tool for centromere mapping of mouse chromosomes.

作者信息

Ceci J D, Matsuda Y, Grubber J M, Jenkins N A, Copeland N G, Chapman V M

机构信息

Mammalian Genetics Laboratory, ABL-Basic Research Program, NCI-Frederick Cancer Research and Development Center, Maryland 21702.

出版信息

Genomics. 1994 Feb;19(3):515-24. doi: 10.1006/geno.1994.1101.

Abstract

Centromere mapping of mouse chromosomes has been problematic due to a paucity of appropriate markers. As a result, the mapping of centromeres has most often relied on the use of Robertsonian chromosomes to mark chromosome ends. Many Robertsonian translocations have been shown to suppress recombination in pericentric regions; therefore, centromere mapping data generated by using Robertsonian chromosomes must be interpreted with caution. We have utilized a new tool for centromere mapping that is applicable to all mouse chromosomes (except the Y chromosome) and that potentially overcomes the inherent limitations of using Robertsonian translocations. Briefly, an interspecific backcross mapping panel was constructed from crosses of C57BL/6Ros and Mus spretus mice. The centromere of each chromosome was subsequently typed by in situ hybridization, using a major satellite probe that uniformly labels C57BL/6Ros centromeres but hybridizes only weakly to M. spretus centromeres. Genetic markers that were already known to map in the proximal region of each of the mouse chromosomes were then typed by segregation analyses of restriction fragment length polymorphisms. These studies have made it possible to align the interspecific genetic map of each of the mouse autosomes and the X chromosome with respect to the centromere. They also provide a basis for comparison with centromere mapping data generated previously by other means.

摘要

由于缺乏合适的标记,小鼠染色体的着丝粒定位一直存在问题。因此,着丝粒的定位最常依赖于使用罗伯逊染色体来标记染色体末端。许多罗伯逊易位已被证明会抑制着丝粒周围区域的重组;因此,使用罗伯逊染色体生成的着丝粒定位数据必须谨慎解读。我们利用了一种新的着丝粒定位工具,该工具适用于所有小鼠染色体(Y染色体除外),并且有可能克服使用罗伯逊易位的固有局限性。简而言之,通过C57BL/6Ros和小家鼠的杂交构建了一个种间回交定位群体。随后,使用主要卫星探针通过原位杂交对每条染色体的着丝粒进行分型,该探针能均匀标记C57BL/6Ros着丝粒,但与小家鼠着丝粒的杂交较弱。然后,通过限制片段长度多态性的分离分析,对已知定位于每条小鼠染色体近端区域的遗传标记进行分型。这些研究使得能够将每条小鼠常染色体和X染色体的种间遗传图谱相对于着丝粒进行比对。它们还为与先前通过其他方法生成的着丝粒定位数据进行比较提供了基础。

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