Nolan-Willard M, Berton M T, Tucker P
University of Texas Southwestern Medical Center, Department of Microbiology, Dallas 75235.
Proc Natl Acad Sci U S A. 1992 Feb 15;89(4):1234-8. doi: 10.1073/pnas.89.4.1234.
We previously documented that a single BCL1 leukemia cell can produce mu and gamma 1 immunoglobulin heavy chains with identical variable segments in an allelically excluded fashion without heavy chain constant region gene rearrangement. To understand the mechanism of dual mu/gamma 1 synthesis in BCL1 subclones, we have analyzed mature and pre-RNA at the nascent and steady-state levels. We find mu and gamma 1 sequences linked in pre-RNA. However, the primary mu and gamma 1 transcription units are about the same length (approximately 15 kilobases). Initiation of gamma 1 pre-RNA occurs upstream of C gamma 1 at sites identical to those seen in lipopolysaccharide/interleukin-4-induced normal B cells. We propose that dual mu/gamma 1 RNA synthesis occurs by a discontinuous transcription mechanism involving either trans-splicing or ligation of mu pre-RNA initiated 5' of the variable-diversity-joining region to gamma 1 pre-RNA initiated 5' of C gamma 1.
我们之前记录到,单个BCL1白血病细胞能够以等位基因排斥的方式产生具有相同可变区的μ和γ1免疫球蛋白重链,而无需重链恒定区基因重排。为了了解BCL1亚克隆中μ/γ1双重合成的机制,我们在新生和稳态水平分析了成熟RNA和前体RNA。我们发现μ和γ1序列在前体RNA中相连。然而,主要的μ和γ1转录单位长度大致相同(约15千碱基)。γ1前体RNA的起始发生在Cγ1上游,其位点与脂多糖/白细胞介素-4诱导的正常B细胞中所见的位点相同。我们提出,μ/γ1双重RNA合成是通过一种不连续转录机制发生的,该机制涉及可变区-多样性区-连接区5'端起始的μ前体RNA与Cγ1 5'端起始的γ1前体RNA之间的反式剪接或连接。