Eicher E M, Washburn L L
Proc Natl Acad Sci U S A. 1978 Feb;75(2):946-50. doi: 10.1073/pnas.75.2.946.
A genetic mapping procedure, called the duplication-deficiency method, is described. This method permits the genetic location of a translocation to be determined within a linkage group without the use of recombination. By utilizing the duplication-deficiency method to define the genetic breakpoints for a series of translocations involving a given chromosome and integrating this information with their cytological breakpoints, obtained by Giemsa banding, a genetic map of the chromosomes is constructed whereby groups of loci are assigned to banded regions. Duplication-deficiency mapping and Giemsa banding analysis of the T(X;7)1Ct and T(7;19)145H translocations together with information from the c25H deletion have permitted mouse chromosome 7 to be divided into six and chromosome 19 into two definable genetic regions.
本文描述了一种名为重复-缺失法的基因定位程序。该方法可在不使用重组的情况下,确定连锁群内易位的基因位置。通过利用重复-缺失法来定义一系列涉及特定染色体的易位的基因断点,并将此信息与通过吉姆萨显带获得的细胞学断点相结合,构建了染色体的基因图谱,据此将基因座组分配到带型区域。对T(X;7)1Ct和T(7;19)145H易位进行重复-缺失定位和吉姆萨显带分析,并结合来自c25H缺失的信息,已使得小鼠7号染色体可被分为六个可定义的基因区域,19号染色体可被分为两个可定义的基因区域。