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A Chemokine Targets the Nucleus: Cxcl12-Gamma Isoform Localizes to the Nucleolus in Adult Mouse Heart

机译:趋化因子靶向核:Cxcl12-Gamma异构体定位到成年小鼠心脏的核。

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摘要

Chemokines are extracellular mediators of complex regulatory circuits involved principally in cell-to-cell communication. Most studies to date of the essential chemokine Cxcl12 (Sdf-1) have focused on the ubiquitously expressed secreted isoforms α and β. Here we show that, unlike these isoforms and all other known chemokines, the alternatively transcribed γ isoform is an intracellular protein that localizes to the nucleolus in differentiated mouse Cardiac tissue. Our results demonstrate that nucleolar transportation is encoded by a nucleolar-localization signal in the unique carboxy-terminal region of Sdf-1γ, and is competent both in vivo and in vitro. The molecular mechanism underlying these unusual chemokine properties involves cardiac-specific transcription of an mRNA containing a unique short-leader sequence lacking the signal peptide and translation from a non-canonical CUG codon. Our results provide an example of genome economy even for essential and highly conserved genes such as Cxcl12, and suggest that chemokines can exert tissue specific functions unrelated to cell-to-cell communication.
机译:趋化因子是主要参与细胞间通讯的复杂调控电路的细胞外介体。迄今为止,大多数关于必需趋化因子Cxcl12(Sdf-1)的研究都集中在普遍表达的分泌型亚型α和β上。在这里,我们表明,与这些同工型和所有其他已知的趋化因子不同,交替转录的γ同工型是一种细胞内蛋白质,其定位于分化小鼠心脏组织中的核仁。我们的结果表明,核仁运输是由Sdf-1γ唯一的羧基末端区域中的核仁定位信号编码的,并且在体内和体外均能胜任。这些异常的趋化因子特性的潜在分子机制涉及含有缺乏信号肽的独特短前导序列的mRNA的心脏特异性转录,以及来自非规范CUG密码子的翻译。我们的结果为甚至重要和高度保守的基因(例如Cxcl12)提供了基因组经济的例子,并表明趋化因子可以发挥与细胞间通讯无关的组织特异性功能。

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