Hirai Atsuko, Tada Mitsuhiro, Furuuchi Keiji, Ishikawa Susumu, Makiyama Kokonoe, Hamada Jun-ichi, Okada Futoshi, Kobayashi Ichiro, Fukuda Hiroshi, Moriuchi Tetsuya
Divisions of Cancer-Related Genes, Institute for Genetic Medicine, Hokkaido University, N-15 W-7, Kita-ku, Sapporo 060-0815, Japan.
Cancer Lett. 2004 Aug 10;211(2):209-18. doi: 10.1016/j.canlet.2004.02.005.
AIE-75 has been known as a 75-kDa autoantigen detected in the serum of autoimmune enteropathy (AIE) and as a colon cancer-related antigen, and now designated as a gene causative of Usher syndrome type 1C hereditary syndromic hearing loss. It binds to a novel putative tumor suppressor MCC2 that is homologous to MCC (mutated in colon cancer) through a PSD-95/Dlg/ZO-1 (PDZ) domain. To clarify the functional role in colon cancer cells, we transfected AIE-75 gene into SW480 colon cancer cells which do not express AIE-75. Expression of AIE-75 suppressed growth of SW480 cells in vitro in correlation with the expression levels. It was due mainly to G2/M phase cell cycle arrest associated with mitotic slippage, resulting in emergence of hyperploid giant-nucleated or multi-nucleated cells. Screening of proteins that bound to PDZ domains of AIE-75 by a yeast two hybrid system showed that three serine/threonine phosphatase catalytic subunits (PP2AC-alpha, PP2AC-beta, and PPP6C) could bind to AIE-75. Since PP2AC is known to regulate G2/M checkpoint, we suggest that AIE-75 interacts with PP2AC and prevent cells to transit mitotic phase.
AIE-75一直被认为是一种在自身免疫性肠病(AIE)血清中检测到的75 kDa自身抗原以及一种与结肠癌相关的抗原,现在被指定为导致1C型Usher综合征遗传性综合征性听力损失的基因。它通过一个PSD-95/Dlg/ZO-1(PDZ)结构域与一种新型的假定肿瘤抑制因子MCC2结合,MCC2与结肠癌中发生突变的MCC同源。为了阐明其在结肠癌细胞中的功能作用,我们将AIE-75基因转染到不表达AIE-75的SW480结肠癌细胞中。AIE-75的表达在体外抑制了SW480细胞的生长,且与表达水平相关。这主要是由于与有丝分裂滑脱相关的G2/M期细胞周期停滞,导致出现超倍体巨核或多核细胞。通过酵母双杂交系统筛选与AIE-75的PDZ结构域结合的蛋白质,结果表明三个丝氨酸/苏氨酸磷酸酶催化亚基(PP2AC-α、PP2AC-β和PPP6C)可以与AIE-75结合。由于已知PP2AC调节G2/M检查点,我们认为AIE-75与PP2AC相互作用并阻止细胞进入有丝分裂期。