Cox D R, Sawicki J A, Yee D, Appella E, Epstein C J
Proc Natl Acad Sci U S A. 1982 Mar;79(6):1930-4. doi: 10.1073/pnas.79.6.1930.
We have assigned the gene (B2m) coding for murine beta 2-microglobulin (B2M) to mouse chromosome 2 by using a novel panel of Chinese hamster-mouse somatic cell hybrid clones. Because of 35 independent primary hybrids used in this study were derived from two types of feral mice, each with a different combination of Robertsonian translocation chromosomes, as well as from mice with a normal complement of acrocentric chromosomes, analysis of 16 selected mouse enzyme markers provided data on the segregation of all 20 mouse chromosomes in these hybrids. Mouse B2M was identified in cell hybrids by immunoprecipitation with a species-specific anti-mouse B2M antiserum followed by two-dimensional polyacrylamide gel electrophoresis of the immunoprecipitated polypeptides. Enzyme analysis of the segregant clones excluded all chromosomes for B2m assignment except mouse chromosome 2, and karyotype analysis of nine informative hybrid clones confirmed the assignment of B2m to this chromosome. These results demonstrate that, in the mouse, as in man, B2m is not linked to the major histocompatibility or immunoglobulin loci.
我们通过使用一组新型的中国仓鼠-小鼠体细胞杂交克隆,将编码小鼠β2-微球蛋白(B2M)的基因(B2m)定位到了小鼠的2号染色体上。由于本研究中使用的35个独立的初级杂交体源自两种野生小鼠,每种野生小鼠具有不同的罗伯逊易位染色体组合,以及源自具有正常近端着丝粒染色体组的小鼠,对16种选定的小鼠酶标记物的分析提供了这些杂交体中所有20条小鼠染色体分离的数据。通过用种特异性抗小鼠B2M抗血清进行免疫沉淀,随后对免疫沉淀的多肽进行二维聚丙烯酰胺凝胶电泳,在细胞杂交体中鉴定出小鼠B2M。对分离克隆的酶分析排除了除小鼠2号染色体外所有用于B2m定位的染色体,对9个信息丰富的杂交克隆的核型分析证实了B2m定位于该染色体。这些结果表明,在小鼠中,与人类一样,B2m不与主要组织相容性或免疫球蛋白基因座连锁。