Khambata S, Mody J, Modzelewski A, Heine D, Passmore H C
Department of Biological Sciences and Bureau of Biological Research, Rutgers University, Piscataway, New Jersey 08855-1059, USA.
Genome Res. 1996 Mar;6(3):195-201. doi: 10.1101/gr.6.3.195.
The majority of recombination events detected within the mouse major histocompatibility complex (MHC) fall into regions of limited physical distance known as hot spots of meiotic recombination. The hot spot associated with the Ea gene appears to be active only in the presence of the p allele carried by the intra-MHC recombinant strain BIO.F(13R). To study the frequency, regulation, and haplotype specificity of recombination at the Ea hot spot, progeny from three different backcrosses involving BIO.F(13R) were screened for recombination events across the MHC using DNA microsatellite markers. Screening of a total of 750 backcross progeny permitted the identification of seven recombinants within the Ea gene. Using restriction site polymorphisms, and sequence-based nucleotide polymorphisms, the recombination breakpoints in all seven Ea recombinants were mapped to two adjacent segments of 71 bp and 346 bp in intron 4 of the Ea gene.
在小鼠主要组织相容性复合体(MHC)中检测到的大多数重组事件都发生在有限物理距离的区域,即减数分裂重组热点。与Ea基因相关的热点似乎仅在MHC内重组菌株BIO.F(13R)携带的p等位基因存在时才活跃。为了研究Ea热点处重组的频率、调控和单倍型特异性,使用DNA微卫星标记对涉及BIO.F(13R)的三个不同回交后代进行筛选,以检测整个MHC区域的重组事件。对总共750个回交后代的筛选使得能够鉴定出Ea基因内的七个重组体。利用限制性位点多态性和基于序列的核苷酸多态性,将所有七个Ea重组体中的重组断点定位到Ea基因内含子4中两个相邻的片段,分别为71 bp和346 bp。