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肿瘤坏死因子区域基因LST1通过差异调控、起始和可变剪接呈现复杂的表达模式。

Complex expression pattern of the TNF region gene LST1 through differential regulation, initiation, and alternative splicing.

作者信息

de Baey A, Fellerhoff B, Maier S, Martinozzi S, Weidle U, Weiss E H

机构信息

Department of Dermatology, University of Munich, Munich, Germany.

出版信息

Genomics. 1997 Nov 1;45(3):591-600. doi: 10.1006/geno.1997.4963.

Abstract

Recently, a novel gene, LST1, was identified in the tumor necrosis factor region of the HLA complex, 4 kb centromeric of the lymphotoxin beta gene. By analyzing several full-length cDNA clones and the genomic DNA, we identified seven exons and four introns, spanning 2.7 kb. Isolation of mouse LST1 cDNA clones established the open reading frame. LST1 transcription is characterized by four alternative transcription initiation sites and extensive alternative splicing. The derived polypeptides vary with regard to the presence of the hydrophobic N-terminus and in short internal sequences. In addition, alternative splicing results in LST1 mRNAs encoding different carboxy-terminal sequences. LST1 is predominantly transcribed in monocytes, and mRNA levels increase upon stimulation with interferon-gamma, with a concomitant change in the mRNA pattern resulting in an enhanced expression of the short LST1 transcripts. These data suggest that LST1 may have a specific role in monocytes and possibly also in T cells. Moreover, we found that the recently published cDNA 1C7 is encoded just centromeric of LST1.

摘要

最近,在HLA复合体的肿瘤坏死因子区域,即淋巴毒素β基因着丝粒侧4 kb处,发现了一个新基因LST1。通过分析几个全长cDNA克隆和基因组DNA,我们确定了7个外显子和4个内含子,跨度为2.7 kb。小鼠LST1 cDNA克隆的分离确定了开放阅读框。LST1转录的特征是有4个可变转录起始位点和广泛的可变剪接。衍生的多肽在疏水N端的存在和短内部序列方面有所不同。此外,可变剪接导致LST1 mRNA编码不同的羧基末端序列。LST1主要在单核细胞中转录,用γ干扰素刺激后mRNA水平升高,同时mRNA模式发生变化,导致短LST1转录本的表达增强。这些数据表明,LST1可能在单核细胞中以及可能在T细胞中具有特定作用。此外,我们发现最近发表的cDNA 1C7编码于LST1的着丝粒侧。

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