Wang C R, Lindahl K F
Howard Hughes Medical Institute, Department of Microbiology, University of Texas Southwestern Medical Center, Dallas 75235-9050.
Immunogenetics. 1993;38(4):258-71. doi: 10.1007/BF00188802.
We have cloned and characterized five new class I genes from the M region at the distal end of the H-2 complex of the BALB/c mouse. M4, M5, and M6 are clustered on two overlapping cosmids, and M7 and M8 are located on another cosmid together with the previously cloned M1 gene, to which they are most closely related. M4, M6, and M7 are full-length class I genes (exons 1 through 5 were identified) but with stop codons or frameshifts that mark them as pseudogenes, and only exons 4 and 5 remain of M8. M5 has complete open reading frames in exons 1 through 5 and intact splice signals; it has the potential to encode a divergent class I major histocompatibility molecule, but no transcripts were found. These genes provide probes for studying the evolution of class I genes in rodents and for the mapping and cloning of genes at the end of the distal inversion in t haplotype chromosomes.
我们已经从BALB/c小鼠H-2复合体远端的M区域克隆并鉴定了五个新的I类基因。M4、M5和M6聚集在两个重叠的黏粒上,M7和M8与先前克隆的M1基因一起位于另一个黏粒上,它们与M1基因关系最为密切。M4、M6和M7是全长I类基因(已鉴定出第1至5外显子),但带有终止密码子或移码突变,表明它们是假基因,而M8仅剩下第4和第5外显子。M5在第1至5外显子中有完整的开放阅读框和完整的剪接信号;它有可能编码一种不同的I类主要组织相容性分子,但未发现转录本。这些基因为研究啮齿动物I类基因的进化以及t单倍型染色体远端倒位末端基因的定位和克隆提供了探针。