Liang Yi, Lyu Chenyang, Xu Shuwen, Tan Chenxin, Jiang Qian, Liu Benquan, Yang Sikai, Huang Weijia, Zhou Ruoning, Yuan Xiaoyi, Zuo Xiaorui, Matsuoka Masao, Ma Guangyong
State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, China.
Department of Hematology, Rheumatology and Infectious Diseases, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
PLoS Pathog. 2025 Jul 28;21(7):e1013381. doi: 10.1371/journal.ppat.1013381. eCollection 2025 Jul.
HTLV-1 is an oncovirus that encodes a transactivator Tax and a regulatory gene HBZ. HTLV-1 early or infectious replication depends on Tax; during HTLV-1 late infection, HBZ plays a crucial role in driving the proliferation of infected cells and maintaining viral persistence. The biphasic replication pattern of HTLV-1 dictated by Tax and HBZ represents a result of viral host adaptation, but how HTLV-1 coordinates Tax and HBZ expression to facilitate early and late infection remains elusive. Here we reveal that HBZ RNA splicing exhibits distinct patterns in Tax+ and Tax- HTLV-1 infected cells. We demonstrate that Tax interacts with the host spliceosome and inhibits HBZ splicing by competitively binding splicing factors including WDR83 and GPATCH1. As a result, Tax confers a natural constraint on HBZ, counterbalancing its anti-replication effect at HTLV-1 early infection, while unleashing HBZ to drive HTLV-1 mitotic propagation during late infection. The splicing-dependent restriction of HBZ by Tax thus represents a critical interplay central to HTLV-1 persistence.
人类嗜T淋巴细胞病毒1型(HTLV-1)是一种致瘤病毒,可编码反式激活因子Tax和调控基因HBZ。HTLV-1的早期或感染性复制依赖于Tax;在HTLV-1晚期感染期间,HBZ在驱动受感染细胞增殖和维持病毒持续性方面发挥关键作用。由Tax和HBZ决定的HTLV-1双相复制模式代表了病毒宿主适应性的结果,但HTLV-1如何协调Tax和HBZ的表达以促进早期和晚期感染仍不清楚。在这里,我们揭示HBZ RNA剪接在Tax+和Tax- HTLV-1感染细胞中表现出不同模式。我们证明Tax与宿主剪接体相互作用,并通过竞争性结合包括WDR83和GPATCH1在内的剪接因子来抑制HBZ剪接。因此,Tax对HBZ施加了自然限制,在HTLV-1早期感染时抵消其抗复制作用,同时在晚期感染时释放HBZ以驱动HTLV-1有丝分裂增殖。因此,Tax对HBZ的剪接依赖性限制代表了HTLV-1持续性的关键相互作用。