Rinchik E M, Russell L B, Copeland N G, Jenkins N A
Genetics. 1986 Feb;112(2):321-42. doi: 10.1093/genetics/112.2.321.
Genes of the dilute-short ear (d-se) region of mouse chromosome 9 comprise an array of loci important to the normal development of the animal. Over 200 spontaneous, chemically induced and radiation-induced mutations at these loci have been identified, making it one of the most genetically well-characterized regions of the mouse. Molecular analysis of this region has recently become feasible by the identification of a dilute mutation that was induced by integration of an ecotropic murine leukemia virus genome. Several unique sequence cellular DNA probes flanking this provirus have now been identified and used to investigate the organization of wild-type chromosomes and chromosomes with radiation-induced d-se region mutations. As expected, several of these mutations are associated with deletions, and, in general, the molecular and genetic complementation maps of these mutants are concordant. Furthermore, a deletion breakpoint fusion fragment has been identified and has been used to orient the physical map of the d-se region with respect to the genetic complementation map. These experiments provide important initial steps for analyzing this developmentally important region at the molecular level, as well as for studying in detail how a diverse group of mutagens acts on the mammalian germline.
小鼠9号染色体上的稀释短耳(d-se)区域的基因包含一系列对动物正常发育至关重要的基因座。在这些基因座上已经鉴定出200多个自发的、化学诱导的和辐射诱导的突变,使其成为小鼠遗传特征最清楚的区域之一。最近,通过鉴定由嗜亲性鼠白血病病毒基因组整合诱导的稀释突变,对该区域进行分子分析变得可行。现在已经鉴定出该前病毒两侧的几个独特序列细胞DNA探针,并用于研究野生型染色体和具有辐射诱导的d-se区域突变的染色体的组织。正如预期的那样,其中一些突变与缺失有关,并且一般来说,这些突变体的分子和遗传互补图谱是一致的。此外,已经鉴定出一个缺失断点融合片段,并已用于相对于遗传互补图谱确定d-se区域的物理图谱。这些实验为在分子水平上分析这个对发育重要的区域以及详细研究多种诱变剂如何作用于哺乳动物种系提供了重要的初步步骤。