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起始于人免疫球蛋白μ重链增强子区域内的mRNA转录本包含一个不可翻译的外显子,并且在5'端极其异质。

mRNA transcripts initiating within the human immunoglobulin mu heavy chain enhancer region contain a non-translatable exon and are extremely heterogeneous at the 5' end.

作者信息

Neale G A, Kitchingman G R

机构信息

Department of Virology and Molecular Biology, St Jude Children's Research Hospital, Memphis, TN 38101.

出版信息

Nucleic Acids Res. 1991 May 11;19(9):2427-33. doi: 10.1093/nar/19.9.2427.

Abstract

Transcription events are thought to precede gene rearrangement in the immunoglobulin (Ig) loci and may be the mechanism by which the various gene regions are made accessible for recombination. If this is the case, identification and characterization of transcripts from the Ig loci should permit a better understanding of the gene rearrangement process. We have isolated a 2.3 kb cDNA clone from the human pre-B cell line Nalm-1 that contains enhancer-specific sequences from the Ig heavy (H) chain gene locus. The 2.3 kb transcript initiated within the enhancer region and showed extreme 5' heterogeneity, with more than 50 initiation sites mapping near the Ig-specific octamer ATTTGCGT. Sequencing of the cDNA clone demonstrated that 644 nucleotides from the Ig enhancer region were incorporated as a leader exon spliced to the mu constant (Cmu) region. This leader exon contained many translation termination codons and may function to inhibit the translation of sterile Cmu polypeptides. Using an enhancer-derived probe, we detected two low-abundancy mRNA transcripts with sizes of 2.3 and 12 kb. Northern blot analysis suggested that the 12 kb transcript was the unspliced precursor mRNA of a VDJ rearrangement. The potential role of these enhancer-containing transcripts in the opening of the IgH chain gene for rearrangement and for class switching is discussed.

摘要

转录事件被认为先于免疫球蛋白(Ig)基因座中的基因重排,并且可能是使各个基因区域可用于重组的机制。如果是这样,对来自Ig基因座的转录本进行鉴定和表征应该有助于更好地理解基因重排过程。我们从人前B细胞系Nalm-1中分离出一个2.3 kb的cDNA克隆,它包含来自Ig重链(H)基因座的增强子特异性序列。这个2.3 kb的转录本在增强子区域内起始,并表现出极端的5'异质性,在Ig特异性八聚体ATTTGCGT附近有超过50个起始位点。对该cDNA克隆的测序表明,来自Ig增强子区域的644个核苷酸被并入作为一个前导外显子,剪接到μ恒定(Cμ)区域。这个前导外显子包含许多翻译终止密码子,可能起到抑制无菌Cμ多肽翻译的作用。使用一个源自增强子的探针,我们检测到两种低丰度的mRNA转录本,大小分别为2.3 kb和12 kb。Northern印迹分析表明,12 kb的转录本是VDJ重排的未剪接前体mRNA。讨论了这些含有增强子的转录本在打开IgH链基因进行重排和类别转换中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f2/329453/0d416f364db9/nar00089-0180-a.jpg

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