Hofker M H, Walter M A, Cox D W
Research Institute, Hospital For Sick Children, Toronto, ON, Canada.
Proc Natl Acad Sci U S A. 1989 Jul;86(14):5567-71. doi: 10.1073/pnas.86.14.5567.
We have found by pulsed-field gel electrophoresis that the human immunoglobulin heavy chain constant region gene complex maps entirely to a 350-kilobase (kb) Mlu I fragment. The enzyme Eag I was used with pulsed-field gel electrophoresis alone and in double digests with Spe I to map the region. C gamma 3, of the C gamma 3-C gamma 1-C psi epsilon 1-C alpha 1 cluster, maps 60 kb to the 3' side of C delta; C gamma 2 of the C gamma 2-C gamma 4-C epsilon-C alpha 2 cluster maps 80 kb to the 3' side of C alpha 1, where C gamma 3 encodes the constant region of the immunoglobulin gamma 3 chain, C gamma 1 encodes the constant region of the immunoglobulin gamma 1 chain, etc. C psi gamma maps 35 kb to the 3' side of C alpha 1 and is in the same transcriptional orientation as the other genes. Although in the cloned DNA many CpG-containing restriction sites were identified, most of these were methylated in peripheral blood leukocytes. The sites that were not methylated were predominantly found in three clusters, or Hpa I tiny fragment islands. One was found on the 5' side of C mu; the other two lie 30 kb to the 3' side of each of the C alpha genes and could indicate the presence of regulatory sequences or genes. A region showing strong linkage disequilibrium between all C gamma genes spans at least 160 kb. The 70-kb C mu-C gamma 3 region, however, shows no linkage disequilibrium, possibly indicating a recombination hot spot. The immunoglobulin heavy chain constant region has been almost entirely cloned and mapped, and thus most rearrangements occurring in this region should be detectable.
我们通过脉冲场凝胶电泳发现,人类免疫球蛋白重链恒定区基因复合体完全定位于一个350千碱基(kb)的Mlu I片段上。酶Eag I单独用于脉冲场凝胶电泳,并与Spe I进行双酶切以定位该区域。Cγ3 - Cγ1 - Cψε1 - Cα1簇中的Cγ3定位于Cδ 3'端60 kb处;Cγ2 - Cγ4 - Cε - Cα2簇中的Cγ2定位于Cα1 3'端80 kb处,其中Cγ3编码免疫球蛋白γ3链的恒定区,Cγ1编码免疫球蛋白γ1链的恒定区等。Cψγ定位于Cα1 3'端35 kb处,且与其他基因转录方向相同。尽管在克隆的DNA中鉴定出许多含CpG的限制性位点,但其中大多数在外周血白细胞中是甲基化的。未甲基化的位点主要集中在三个簇或Hpa I微小片段岛中。一个位于Cμ的5'端;另外两个位于每个Cα基因3'端30 kb处,可能表明存在调控序列或基因。所有Cγ基因之间显示出强连锁不平衡的区域跨度至少为160 kb。然而,70 kb的Cμ - Cγ3区域未显示连锁不平衡,这可能表明存在一个重组热点。免疫球蛋白重链恒定区几乎已全部被克隆和定位,因此该区域发生的大多数重排应该是可检测到的。