Orita S, Takagi S, Saiga A, Minoura N, Araki K, Kinoshita K, Kondo T, Hinuma Y, Igarashi H
Shionogi Institute for Medical Science, Osaka, Japan.
J Gen Virol. 1992 Sep;73 ( Pt 9):2283-9. doi: 10.1099/0022-1317-73-9-2283.
Although the p21X protein of human T cell leukaemia virus type 1 (HTLV-1) is generally thought to be expressed from a doubly spliced mRNA transcript (tax/rex mRNA) that encodes the p40tax, p27rex and p21X proteins, we have shown previously that a novel, alternatively spliced mRNA transcript (p21X mRNA) is responsible for p21X production in HTLV-1-infected cell lines. In the present study, we analysed expression of p21X mRNA and tax/rex mRNA in uncultured and cultured peripheral blood mononuclear cells (PBMCs) from eight patients with adult T cell leukaemia by using a quantitative polymerase chain reaction coupled to reverse transcription. The results demonstrated that the expression of p21X mRNA occurs constitutively in all uncultured and cultured PBMCs, whereas the expression of tax/rex mRNA is inducible in the cultured PBMCs, as described previously. In uncultured and cultured PBMCs from the one specimen in which p21X mRNA was highly expressed, the p21X protein was detectable by Western blotting. On the other hand, p27rex protein was detectable only after cultivation. These findings indicate that p21X mRNA is constitutively expressed in vivo and is responsible for production of p21X protein.
尽管人们普遍认为,人类嗜T淋巴细胞病毒1型(HTLV-1)的p21X蛋白是由一种双剪接的mRNA转录本(tax/rex mRNA)表达产生的,该转录本编码p40tax、p27rex和p21X蛋白,但我们之前已经表明,一种新的选择性剪接的mRNA转录本(p21X mRNA)负责在HTLV-1感染的细胞系中产生p21X。在本研究中,我们通过使用逆转录定量聚合酶链反应,分析了8例成人T细胞白血病患者未培养和培养的外周血单个核细胞(PBMC)中p21X mRNA和tax/rex mRNA的表达情况。结果表明,p21X mRNA在所有未培养和培养的PBMC中组成性表达,而tax/rex mRNA的表达在培养的PBMC中是可诱导的,如先前所述。在p21X mRNA高度表达的一个样本的未培养和培养的PBMC中,通过蛋白质免疫印迹法可检测到p21X蛋白。另一方面,仅在培养后才可检测到p27rex蛋白。这些发现表明,p21X mRNA在体内组成性表达,并负责p21X蛋白的产生。