Decker D J, Boyle N E, Klinman N R
Department of Immunology, Scripps Clinic and Research Foundation, La Jolla, CA 92037.
J Immunol. 1991 Aug 15;147(4):1406-11.
Ig H chain V regions using the VH81X gene segment were PCR amplified from genomic DNA obtained from either splenic B cells or surface (s)Ig- bone marrow cells of BALB/c mice. Sequence analysis demonstrated that 93% of VH81X containing H chain V region genes in splenic B cells were rearranged nonproductively. Furthermore, 74% of rearrangements of VH81X among sIg- bone marrow cells were nonproductive. This contrasts with previous results obtained for rearrangements of members of the VH36-60 gene segment family among sIg- cells wherein, as a consequence of extensive clonal expansion after productive H chain V gene rearrangement, 80% of rearrangements were productive. The low proportion of productive rearrangements of VH81X is interpreted as indicating that most productive rearrangements of VH81X cannot facilitate clonal expansion, which would support the hypothesis that selection for clonal expansion and maturation is dependent on the amino acid sequence of nascent H chains. Additionally, because most productive rearrangements of VH81X cannot facilitate clonal maturation but do appear to mediate allelic exclusion, these processes are likely to be regulated independently.
利用VH81X基因片段的Ig重链V区,通过聚合酶链反应(PCR)从BALB/c小鼠脾脏B细胞或表面(s)Ig阴性骨髓细胞获得的基因组DNA中扩增得到。序列分析表明,脾脏B细胞中93%含有VH81X的重链V区基因重排无功能。此外,sIg阴性骨髓细胞中VH81X重排的74%无功能。这与之前在sIg阴性细胞中VH36 - 60基因片段家族成员重排的结果形成对比,在后者中,由于有功能的重链V基因重排后广泛的克隆扩增,80%的重排是有功能的。VH81X有功能重排的低比例被解释为表明VH81X的大多数有功能重排不能促进克隆扩增,这将支持克隆扩增和成熟的选择取决于新生重链氨基酸序列的假说。此外,由于VH81X的大多数有功能重排不能促进克隆成熟,但似乎能介导等位基因排斥,这些过程可能是独立调控的。