Agoston Denes V, Szemes Marianna, Dobi Albert, Palkovits Miklos, Georgopoulos Katia, Gyorgy Andrea, Ring Mary A
Department of Anatomy, Physiology and Genetics, USUHS, Bethesda, Maryland, USALCB, NIMH, NIH, Bethesda, Maryland, USACutaneous Biology Research Center, MGH, Harvard Medical School, Charlestown, Massachusetts, USAGraduate Program in Genetics, The George Washington University, Washington, District of Columbia, USA.
J Neurochem. 2007 Sep;102(6):1805-1816. doi: 10.1111/j.1471-4159.2007.04653.x. Epub 2007 May 14.
The Ikaros (Ik) gene encodes alternatively spliced zinc-finger proteins originally identified in developing hematopoietic organs and acts as master regulator of lymphoid development. During our search for transcription factors that control the developmental expression of the enkephalin (ENK) gene we found that Ik-1 and Ik-2 isoforms are specifically expressed in the embryonic striatum and bind the Ik-like cis-regulatory DNA element present on the ENK gene. Ik proteins are expressed by both proliferating (BrdU+/nestin+) and by post-mitotic differentiating (MAP2+) cells in the developing striatum between embryonic day 12 and post-natal day 2 and mRNAs encoding for the Ik and ENK genes are co-expressed by a subset of differentiating striatal neurons. Blocking the DNA binding of Ik proteins in differentiating embryonic striatal neuronal cultures resulted in decreased ENK expression and mutant animals lacking the DNA-binding domain of Ik had a deficit in the number of ENK but not in dynorphin or substance P mRNA+ cells. Animals lacking the protein interaction domain of Ik showed no deficit. These results demonstrate that Ik-1 and Ik-2 proteins through their DNA binding act as positive regulators of ENK gene expression in the developing striatum and participate in regulating enkephalinergic differentiation.
伊卡洛斯(Ik)基因编码最初在发育中的造血器官中发现的可变剪接锌指蛋白,并作为淋巴样发育的主要调节因子。在我们寻找控制脑啡肽(ENK)基因发育表达的转录因子的过程中,我们发现Ik-1和Ik-2亚型在胚胎纹状体中特异性表达,并与ENK基因上存在的Ik样顺式调节DNA元件结合。在胚胎第12天至出生后第2天之间的发育中的纹状体中,增殖细胞(BrdU+/巢蛋白+)和有丝分裂后分化细胞(MAP2+)均表达Ik蛋白,并且编码Ik和ENK基因的mRNA由一部分分化的纹状体神经元共同表达。在分化的胚胎纹状体神经元培养物中阻断Ik蛋白的DNA结合会导致ENK表达降低,而缺乏Ik DNA结合结构域的突变动物在ENK数量上有缺陷,但强啡肽或P物质mRNA+细胞数量没有缺陷。缺乏Ik蛋白相互作用结构域的动物没有表现出缺陷。这些结果表明,Ik-1和Ik-2蛋白通过其DNA结合作用,在发育中的纹状体中作为ENK基因表达的正调节因子,并参与调节脑啡肽能分化。