外显子
生物
选择性拼接
分子生物学
基因亚型
串联外显子复制
RNA剪接
基因
剪接
打开阅读框
终止密码子
细胞生物学
遗传学
肽序列
核糖核酸
作者
Christian Nielsen,Line Ohm‐Laursen,Torben Barington,Steffen Husby,Søren Thue Lillevang
标识
DOI:10.1016/j.cellimm.2005.07.007
摘要
PD-1 is an immunoregulatory receptor expressed on the surface of activated T cells, B cells, and monocytes. We describe four alternatively spliced PD-1 mRNA transcripts (PD-1Δex2, PD-1Δex3, PD-1Δex2,3, and PD-1Δex2,3,4) in addition to the full length isoform. PD-1Δex2 and PD-1Δex3 are generated by alternative splicing where exon 2 (extracellular IgV-like domain) and exon 3 (transmembrane domain) respectively are spliced out. PD-1Δex3 is therefore likely to encode a soluble form of PD-1. PD-1Δex2,3 lacks exon 2 and 3. These three variants have unaffected open reading frames. PD-1Δex2,3,4 lacks exon 2, 3, and 4 (intracellular domain) and contains a premature stop codon in exon 5. Activation of human PBMCs with anti-CD3 + anti-CD28 monoclonal antibodies induces an increased level of each PD-1 transcript. A parallel increase in the expression of PD-1Δex3 and flPD-1 upon activation suggests an important interplay between the putative soluble PD-1 and flPD-1 possibly involved in maintenance of peripheral self-tolerance and prevention of autoimmunity.
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