Leung Sara W, Apponi Luciano H, Cornejo Omar E, Kitchen Chad M, Valentini Sandro R, Pavlath Grace K, Dunham Christine M, Corbett Anita H
Department of Biochemistry, Emory University School of Medicine, 1510 Clifton Road, N.E., Atlanta, GA 30322-2430, USA.
Gene. 2009 Jun 15;439(1-2):71-8. doi: 10.1016/j.gene.2009.02.022. Epub 2009 Mar 18.
The human ZC3H14 gene encodes an evolutionarily conserved Cys(3)His zinc finger protein that binds specifically to polyadenosine RNA and is thus postulated to modulate post-transcriptional gene expression. Expressed sequence tag (EST) data predicts multiple splice variants of both human and mouse ZC3H14. Analysis of ZC3H14 expression in both human cell lines and mouse tissues confirms the presence of multiple alternatively spliced transcripts. Although all of these transcripts encode protein isoforms that contain the conserved C-terminal zinc finger domain, suggesting that they could all bind to polyadenosine RNA, they differ in other functionally important domains. Most of the alternative transcripts encode closely related proteins (termed isoforms 1, 2, 3, and 3 short) that differ primarily in the inclusion of three small exons, 9, 10, and 11, resulting in predicted protein isoforms ranging from 82 to 64 kDa. Each of these closely related isoforms contains predicted classical nuclear localization signals (cNLS) within exons 7 and 11. Consistent with the presence of these putative nuclear targeting signals, these ZC3H14 isoforms are all localized to the nucleus. In contrast, an additional transcript encodes a smaller protein (34 kDa) with an alternative first exon (isoform 4). Consistent with the absence of the predicted cNLS motifs located in exons 7 and 11, ZC3H14 isoform 4 is localized to the cytoplasm. Both EST data and experimental data suggest that this variant is enriched in testes and brain. Using an antibody that detects endogenous ZC3H14 isoforms 1-3 reveals localization of these isoforms to nuclear speckles. These speckles co-localize with the splicing factor, SC35, suggesting a role for nuclear ZC3H14 in mRNA processing. Taken together, these results demonstrate that multiple transcripts encoding several ZC3H14 isoforms exist in vivo. Both nuclear and cytoplasmic ZC3H14 isoforms could have distinct effects on gene expression mediated by the common Cys(3)His zinc finger polyadenosine RNA binding domain.
人类ZC3H14基因编码一种进化上保守的Cys(3)His锌指蛋白,该蛋白特异性结合多聚腺苷酸RNA,因此推测其可调节转录后基因表达。表达序列标签(EST)数据预测了人类和小鼠ZC3H14的多种剪接变体。对人类细胞系和小鼠组织中ZC3H14表达的分析证实了多种选择性剪接转录本的存在。尽管所有这些转录本都编码包含保守C端锌指结构域的蛋白质异构体,这表明它们都可以结合多聚腺苷酸RNA,但它们在其他功能重要结构域上存在差异。大多数选择性转录本编码密切相关的蛋白质(称为异构体1、2、3和3短),它们主要在包含三个小外显子9、10和11方面存在差异,导致预测的蛋白质异构体大小范围为82至64 kDa。这些密切相关的异构体中的每一个在第7和11外显子中都含有预测的经典核定位信号(cNLS)。与这些假定的核靶向信号的存在一致,这些ZC3H14异构体都定位于细胞核。相比之下,另一种转录本编码一种较小的蛋白质(34 kDa),其具有替代的第一个外显子(异构体4)。与第7和11外显子中预测的cNLS基序缺失一致,ZC3H14异构体4定位于细胞质。EST数据和实验数据均表明,这种变体在睾丸和大脑中富集。使用检测内源性ZC3H14异构体1 - 3的抗体显示这些异构体定位于核斑点。这些斑点与剪接因子SC35共定位,表明核内ZC3H14在mRNA加工中发挥作用。综上所述,这些结果表明体内存在编码几种ZC3H14异构体的多种转录本。核内和胞质中的ZC3H14异构体可能对由共同的Cys(3)His锌指多聚腺苷酸RNA结合结构域介导的基因表达产生不同影响。