Goh S H, Park J H, Lee Y J, Lee H G, Yoo H S, Lee I C, Park J H, Kim Y S, Lee C C
Genome Research Center, Korea Research Institute of Bioscience and Biotechnology, Taejon, 305-333, Korea.
Genomics. 2000 Nov 15;70(1):1-18. doi: 10.1006/geno.2000.6342.
The development of immature thymocytes to mature T-lymphocytes is a central process for establishing a functional immune system. The gene regulatory events involved in this process are of outstanding interest in understanding the generation of the T-cell repertoire as well as the differentiation of lineage-specific cells, such as CD4(+) helper T-cells or CD8(+) cytotoxic T-lymphocytes. While some essential genes involved in lineage decision and thymocyte differentiation have been already identified, the exact regulatory mechanisms and differential gene expressions are still unknown. The present study was performed to analyze the gene expression profile during T-cell development, in particular, during the differentiation of immature thymocytes into CD4(+) mature T-cells by analyses of expressed sequence tags (ESTs), and to elucidate novel human genes involved in this process. Based on distinct developmental stages, three PCR-based cDNA libraries from immature CD3(-),4(-),8(-) triple-negative, CD4(+),8(+) double-positive, and mature CD4(+),8(-) single-positive thymocytes were constructed. A total of 1477 randomly selected clones were analyzed by automated single-pass sequencing, and the assembly of ESTs resulted in 1027 different species of contig sequences. Among them, 392 contig sequences were matched to known genes, and several novel transcripts were discovered. The matched clones were classified into seven categories according to their functional aspects, and the gene expression profiles of the three thymocyte subsets were compared. The information obtained in current study will serve as a valuable resource for elucidating the molecular mechanism of intrathymic T-cell development.
未成熟胸腺细胞发育为成熟T淋巴细胞是建立功能性免疫系统的核心过程。这一过程中涉及的基因调控事件对于理解T细胞库的产生以及谱系特异性细胞(如CD4(+)辅助性T细胞或CD8(+)细胞毒性T淋巴细胞)的分化具有重要意义。虽然已经确定了一些参与谱系决定和胸腺细胞分化的关键基因,但确切的调控机制和差异基因表达仍不清楚。本研究旨在通过分析表达序列标签(EST)来分析T细胞发育过程中的基因表达谱,特别是未成熟胸腺细胞向CD4(+)成熟T细胞分化过程中的基因表达谱,并阐明参与这一过程的新的人类基因。基于不同的发育阶段,构建了来自未成熟CD3(-)、4(-)、8(-)三阴性、CD4(+)、8(+)双阳性和成熟CD4(+)、8(-)单阳性胸腺细胞的三个基于PCR的cDNA文库。通过自动单通道测序分析了总共1477个随机选择的克隆,EST的组装产生了1027种不同的重叠群序列。其中,392个重叠群序列与已知基因匹配,并发现了一些新的转录本。根据其功能方面将匹配的克隆分为七类,并比较了三个胸腺细胞亚群的基因表达谱。本研究获得的信息将作为阐明胸腺内T细胞发育分子机制的宝贵资源。