Blaud Magali, Vossen Christine, Joseph Gérard, Alazard Robert, Erard Monique, Nieto Laurence
Laboratoire de Pharmacologie et de Biologie Structurale, CNRS UPR 9062, 205, route de Narbonne, 31077 Toulouse Cedex, France.
J Mol Biol. 2004 Jun 18;339(5):1049-58. doi: 10.1016/j.jmb.2004.04.035.
N Oct-3, a neurospecific POU protein, homodimerizes in a non-cooperative fashion on the neuronal aromatic l-amino acid decarboxylase gene promoter and generates heterodimers with HNF-3beta. Several other neuronal gene promoters, the corticotropin releasing hormone and the aldolase C gene promoters also contain overlapping binding sites for N Oct-3 and HNF-3beta. We have demonstrated that N Oct-3 presents a non-cooperative homodimerization on these two additional targets and can also give rise to heterodimers with HNF-3beta. Surprisingly, despite the high degree of conservation of the respective POU subunits, the ubiquitous POU protein Oct-1 can only form monomers even in the presence of either N Oct-3 or HNF-3beta on these DNA targets. Our data indicate that this difference is correlated with the specific ability of a portion of the N Oct-3 linker to fold as an alpha-helix, a property shared by class III POU proteins. These results suggest that this novel binding pattern permits the heterodimerization of N Oct-3 and HNF-3beta on the neuronal promoters, which could be a key issue in the development of the nervous system and possibly tumors of neural origin.
10月3日,一种神经特异性POU蛋白以非协同方式在神经元芳香族L-氨基酸脱羧酶基因启动子上形成同源二聚体,并与HNF-3β形成异源二聚体。其他几个神经元基因启动子,促肾上腺皮质激素释放激素和醛缩酶C基因启动子也含有N Oct-3和HNF-3β的重叠结合位点。我们已经证明,N Oct-3在这两个额外的靶点上呈现非协同同源二聚化,并且也能与HNF-3β形成异源二聚体。令人惊讶的是,尽管各自的POU亚基高度保守,但普遍存在的POU蛋白Oct-1即使在这些DNA靶点上存在N Oct-3或HNF-3β的情况下也只能形成单体。我们的数据表明,这种差异与N Oct-3连接子的一部分折叠成α-螺旋的特定能力相关,这是III类POU蛋白共有的特性。这些结果表明,这种新的结合模式允许N Oct-3和HNF-3β在神经元启动子上异源二聚化,这可能是神经系统发育以及可能的神经源性肿瘤发生中的一个关键问题。