Department of Laboratory Medicine, Division of Pathology, Karolinska Institutet and Karolinska University Hospital Huddinge, Stockholm, Sweden.
PLoS One. 2010 Nov 22;5(11):e14085. doi: 10.1371/journal.pone.0014085.
The SRY (sex determining region Y)-box 11 (SOX11) gene, located on chromosome 2p25, encodes for a transcription factor that is involved in tissue remodeling during embryogenesis and is crucial for neurogenesis. The role for SOX11 in hematopoiesis has not yet been defined. Two genes under direct control of SOX11 are the class- III β-tubulin gene (TUBB3) in neural cells and the transcription factor TEA domain family member 2 (TEAD2) in neural and mesenchymal progenitor cells. Normal, mature lymphocytes lack SOX11 but express SOX4, another member of the same group of SOX transcription factors. We and others recently identified SOX11 as aberrantly expressed in mantle cell lymphoma (MCL). Since SOX11 is variably expressed in MCL it may not be essential for tumorigenesis, but may carry prognostic information. Currently, no specific functional effects have been linked to SOX11 expression in MCL and it is not known which genes are under influence of SOX11 in lymphoma. In this study we found variable expression of SOX11, SOX4 and SOX12 mRNA in mantle cell lymphoma cell lines. Downregulation of SOX11 expression by siRNA verified that SOX11 controlled the expression of the gene TUBB3 in the MCL cell line Granta 519. Furthermore we identified, by global gene expression analysis, 26 new target genes influenced by siRNA SOX11 downmodulation. Among these genes, DBN1, SETMAR and HIG2 were found to be significantly correlated to SOX11 expression in two cohorts of primary mantle cell lymphomas. Chromatin immunoprecipitation (ChIP) analysis showed that these genes are direct targets of the SOX11 protein. In spite of almost complete downregulation of the SOX11 protein no significant effects on Granta 519 cell proliferation or survival in short term in vitro experiments was found. In summary we have identified a number of genes influenced by SOX11 expression in MCL cell lines and primary MCL. Among these genes, DBN1, SETMAR and HIG2 are direct transcriptional targets of the SOX11 protein.
SRY (性别决定区 Y)-框 11 (SOX11 )基因位于染色体 2p25 上,编码一种转录因子,该转录因子参与胚胎发生过程中的组织重塑,对于神经发生至关重要。SOX11 在造血中的作用尚未确定。SOX11 直接控制的两个基因是神经细胞中的 III 类 β-微管蛋白基因(TUBB3)和神经和间充质祖细胞中的转录因子 TEA 结构域家族成员 2(TEAD2)。正常成熟的淋巴细胞缺乏 SOX11,但表达另一个 SOX 转录因子家族的成员 SOX4。我们和其他人最近发现 SOX11 在套细胞淋巴瘤(MCL)中异常表达。由于 SOX11 在 MCL 中的表达是可变的,因此它可能不是肿瘤发生所必需的,但可能具有预后信息。目前,尚未将 SOX11 在 MCL 中的表达与特定的功能效应联系起来,也不知道哪些基因受淋巴瘤中 SOX11 的影响。在这项研究中,我们发现套细胞淋巴瘤细胞系中 SOX11、SOX4 和 SOX12 mRNA 的表达存在差异。通过 siRNA 下调 SOX11 表达证实,SOX11 控制 MCL 细胞系 Granta 519 中 TUBB3 基因的表达。此外,通过全基因表达分析,我们鉴定了 26 个新的受 siRNA SOX11 下调影响的靶基因。在两个原发性套细胞淋巴瘤队列中,发现 DBN1、SETMAR 和 HIG2 基因与 SOX11 表达显著相关。染色质免疫沉淀(ChIP)分析表明,这些基因是 SOX11 蛋白的直接靶基因。尽管 SOX11 蛋白的表达几乎完全下调,但在短期的体外实验中,未发现对 Granta 519 细胞增殖或存活有明显影响。总之,我们已经确定了一些受 MCL 细胞系和原发性 MCL 中 SOX11 表达影响的基因。在这些基因中,DBN1、SETMAR 和 HIG2 是 SOX11 蛋白的直接转录靶基因。