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艾贝尔逊鼠白血病病毒转化的淋巴样细胞系中的多种免疫球蛋白重链基因转录物

Multiple immunoglobulin heavy-chain gene transcripts in Abelson murine leukemia virus-transformed lymphoid cell lines.

作者信息

Alt F W, Rosenberg N, Enea V, Siden E, Baltimore D

出版信息

Mol Cell Biol. 1982 Apr;2(4):386-400. doi: 10.1128/mcb.2.4.386-400.1982.

DOI:10.1128/mcb.2.4.386-400.1982
PMID:6810096
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC369803/
Abstract

Lymphoid cells transformed by Abelson murine leukemia virus (A-MuLV) contain three classes of RNA transcripts from immunoglobulin mu genes. P mu-mRNAs (productive) correspond to the normal 2.7-kilobase (kb) membrane (mu m) and 2.4-kb secreted (mu s) mu mRNA species both in size and coding capacity and occur at approximately equal abundance in most mu-positive (pre-B-like) A-MuLV transformants. A mu-mRNAs (aberrant) generally fall into one of two categories--aberrantly small 2.3-kb mu m and 2.0-kb mu s mRNAs which encode aberrantly small mu polypeptide chains, or normal-sized, V H-containing mu RNAs which do not encode immunologically identifiable mu polypeptide chains. In one case, the latter type of A mu-mRNA was demonstrated to result from an in-phase termination codon in the D segment of the mu mRNA. Also, most, if not all, A-MuLV transformants express members of a 3.0 to 1.9-kb set of C mu-containing, but V H-negative S mu-RNAs (for sterile), the expression of which may occur simultaneously with but independently of P mu-mRNAs or A mu-mRNAs. The S mu-RNA sequences do not encode immunologically identifiable mu chains and can be produced by cells with unrearranged heavy-chain alleles, such as T-lymphocytes, although the structure of the S mu-RNAs from T-lymphoid cells appears to be different from that of B-lymphoid cell S mu-RNAs. Certain A-MuLV transformants also express gamma-RNA sequences that are probably analogous to the three different forms of mu RNA. These data support the concept that heavy-chain allelic exclusion, like that of light chains, is not mediated by control at the DNA or RNA levels but is probably a consequence of feedback control from cytoplasmic mu chains.

摘要

由阿贝尔森鼠白血病病毒(A-MuLV)转化的淋巴细胞含有三类来自免疫球蛋白μ基因的RNA转录本。Pμ-mRNAs(有功能的)在大小和编码能力上与正常的2.7千碱基(kb)膜(μm)和2.4-kb分泌型(μs)μ mRNA种类相对应,并且在大多数μ阳性(前B样)A-MuLV转化体中以大致相等的丰度出现。Aμ-mRNAs(异常的)通常分为两类之一——编码异常小的μ多肽链的异常小的2.3-kbμm和2.0-kbμs mRNAs,或者不编码免疫可识别的μ多肽链的正常大小、含VH的μRNAs。在一个案例中,后一种类型的Aμ-mRNA被证明是由μ mRNA的D区段中的同相终止密码子导致的。此外,大多数(如果不是全部)A-MuLV转化体表达一组3.0至1.9-kb的含Cμ但VH阴性的Sμ-RNAs(无菌的)成员,其表达可能与Pμ-mRNAs或Aμ-mRNAs同时发生但独立于它们。Sμ-RNA序列不编码免疫可识别的μ链,并且可以由具有未重排重链等位基因的细胞产生,例如T淋巴细胞,尽管来自T淋巴细胞的Sμ-RNAs的结构似乎与B淋巴细胞Sμ-RNAs的结构不同。某些A-MuLV转化体还表达可能类似于三种不同形式的μ RNA的γ-RNA序列。这些数据支持这样的概念,即重链等位基因排斥,如同轻链的情况一样,不是由DNA或RNA水平的控制介导的,而是可能是细胞质μ链反馈控制的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/4d478ec6d8f7/molcellb00116-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/f19d8d99e1b2/molcellb00116-0056-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/00b1ce57a9b7/molcellb00116-0057-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/bae0fda4cedf/molcellb00116-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/cc8b56e4b110/molcellb00116-0060-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/3e2a7ebf9c9a/molcellb00116-0062-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/4d478ec6d8f7/molcellb00116-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/f19d8d99e1b2/molcellb00116-0056-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/00b1ce57a9b7/molcellb00116-0057-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/bae0fda4cedf/molcellb00116-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/cc8b56e4b110/molcellb00116-0060-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/3e2a7ebf9c9a/molcellb00116-0062-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b27/369803/4d478ec6d8f7/molcellb00116-0063-a.jpg

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Generation of long mRNA for membrane immunoglobulin gamma 2a chains by differential splicing.通过可变剪接产生用于膜免疫球蛋白γ2a链的长mRNA。
Nature. 1981 Oct 1;293(5831):406-8. doi: 10.1038/293406a0.
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