Selsing E, Storb U
Nucleic Acids Res. 1981 Nov 11;9(21):5725-35. doi: 10.1093/nar/9.21.5725.
Five families of variable region genes of mouse kappa chains were analyzed by Southern blot hybridization to determine their relative chromosomal map positions. Map positions were deduced by Vk gene deletion from antibody-producing cells expressing upstream Vk genes and retention in cells expressing downstream genes. The Vk regions expressed in the myelomas M0PC167, MPC11, M0PC21 and ABPC20 are members of Vk families exhibiting one, three, six and six major germline hybridization bands respectively. The gene order of the five families in germline DNA was found to be VM167-VM11-(VM21, VA20)-VABE8-Jk-Ck. As expected in a deletion model of immunoglobulin gene rearrangement, a sequence located just 5' of J1 in germline DNA was found to be absent from some antibody producing cells which had not retained any germline Ck genes. However, other cell lines contained this sequence in rearranged contexts, suggesting that any deletion model of immunoglobulin V-J joining, as well as V gene mapping, must take into account the possibilities of stepwise rearrangements and reintegration of "deleted" DNA.
通过Southern印迹杂交分析了小鼠κ链可变区基因的五个家族,以确定它们相对的染色体图谱位置。图谱位置是通过从表达上游Vk基因的抗体产生细胞中Vk基因缺失以及在表达下游基因的细胞中保留来推断的。骨髓瘤M0PC167、MPC11、M0PC21和ABPC20中表达的Vk区域分别是Vk家族的成员,这些家族分别显示出1条、3条、6条和6条主要的种系杂交带。发现种系DNA中五个家族的基因顺序为VM167-VM11-(VM21, VA20)-VABE8-Jk-Ck。正如在免疫球蛋白基因重排的缺失模型中所预期的那样,在一些没有保留任何种系Ck基因的抗体产生细胞中,发现种系DNA中位于J1 5'端的一个序列缺失。然而,其他细胞系在重排的情况下含有该序列,这表明免疫球蛋白V-J连接以及V基因定位的任何缺失模型都必须考虑“缺失”DNA逐步重排和重新整合的可能性。