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μ链和γ1重链的共表达可通过来自同一条未重排染色体的不连续转录机制发生。

Coexpression of mu and gamma 1 heavy chains can occur by a discontinuous transcription mechanism from the same unrearranged chromosome.

作者信息

Nolan-Willard M, Berton M T, Tucker P

机构信息

University of Texas Southwestern Medical Center, Department of Microbiology, Dallas 75235.

出版信息

Proc Natl Acad Sci U S A. 1992 Feb 15;89(4):1234-8. doi: 10.1073/pnas.89.4.1234.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9589/48423/aa61fae844ef/pnas01078-0095-a.jpg

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