Sasso E H, Johnson T, Kipps T J
Division of Rheumatology, University of Washington, Seattle 98105, USA.
J Clin Invest. 1996 May 1;97(9):2074-80. doi: 10.1172/JCI118644.
51p1 is an immunoglobulin VH gene that is frequently expressed in B cell chronic lymphocytic leukemia and early in B cell ontogeny. The 51p1 gene locus is highly polymorphic, consisting of 13 alleles that can be classified as being either 51p1-related or hy1263-related, based on distinctive sequence motifs in the second complementarity determining region. Two of the 51p1-related genes usually occur as a linked pair on the same haopltype, resulting from gene duplication. Consequently, a person can have a total of zero to four copies of 51p1-related genes. These genes are detectable in genomic DNA by sequence-specific RFLP analysis using oligonucleotide probes. Ig encoded by nonmutated 51p1-related genes can be detected by G6, a murine antiidiotypic mAb. We have now studied lymphocytes from 35 human tonsils to examine the relation between the number of 51p1-related germlime gene copies and the proportion of IgD-bearing tonsillar B cells that react with G6. All subjects who had zero copies of 51p1-related genes lacked any G6-reactive B cells, whereas those with four copies of 51p1-related genes had the highest proportions of G6-positive IgD B cells, up to 11.4%. Subjects with intermediate gene doses had intermediate proportions of G6-reactive B cells. Over the entire data set, the percentage of IgD-bearing B cells that reacted with G6 was proportional to the 51p1-related gene copy number (r = 0.92, p < 0.001), with each copy accounting for 2.4-4.0% of the IgD-bearing B cells. We conclude that 51p1-related genes are expressed by a relatively large percentage of IgD+ tonsillar B cells and this percentage is proportional to the germline copy number of 51p1-related genes.
51p1是一种免疫球蛋白VH基因,在B细胞慢性淋巴细胞白血病以及B细胞个体发育早期经常表达。51p1基因座具有高度多态性,由13个等位基因组成,根据第二互补决定区的独特序列基序,可分为51p1相关或hy1263相关。51p1相关基因中的两个通常作为同一单倍型上的连锁对出现,这是基因复制的结果。因此,一个人可能总共拥有零至四个51p1相关基因拷贝。使用寡核苷酸探针通过序列特异性RFLP分析可在基因组DNA中检测到这些基因。由未突变的51p1相关基因编码的Ig可通过鼠抗独特型单克隆抗体G6检测到。我们现在研究了来自35个人扁桃体的淋巴细胞,以检查51p1相关种系基因拷贝数与与G6反应的含IgD扁桃体B细胞比例之间的关系。所有没有51p1相关基因拷贝的受试者都缺乏任何与G6反应的B细胞,而那些有四个51p1相关基因拷贝的受试者具有最高比例的G6阳性IgD B细胞,高达11.4%。基因剂量中等的受试者具有中等比例的与G6反应的B细胞。在整个数据集中,与G6反应的含IgD B细胞百分比与51p1相关基因拷贝数成正比(r = 0.92,p < 0.001),每个拷贝占含IgD B细胞的2.4 - 4.0%。我们得出结论,51p1相关基因在相对较大比例的IgD +扁桃体B细胞中表达,并且该百分比与51p1相关基因的种系拷贝数成正比。