Taelman Vincent, Van Wayenbergh Réginald, Sölter Marion, Pichon Bruno, Pieler Tomas, Christophe Daniel, Bellefroid Eric J
Laboratoire d'Embryologie Moléculaire, Université Libre de Bruxelles, Institut de Biologie et de Médecine Moléculaires (IBMM), rue des Profs. Jeener et Brachet 12, B-6041 Gosselies, Belgium.
Dev Biol. 2004 Dec 1;276(1):47-63. doi: 10.1016/j.ydbio.2004.08.019.
XHRT1 is a member of the HRT/Hey protein subfamily that are known as Notch effectors. XHRT1 is expressed in the developing floor plate and encodes a basic helix-loop-helix (bHLH) transcription repressor. Here, we show that XHRT1 misexpression in the neural plate inhibits differentiation of neural precursor cells and thus may be important for floor plate cells to prevent them from adopting a neuronal fate. Deletion analysis indicated that inhibition of differentiation by XHRT1 requires the DNA-binding bHLH motif and either the Orange domain or the C-terminal region. XHRT1 could efficiently homodimerize and heterodimerize with hairy proteins. Among those hairy genes, Xhairy2b shows extensive overlap of expression with XHRT1 in floor plate precursors and may be a biologically relevant XHRT1 partner. Dimerization is mediated through both the bHLH and downstream sequences, the Orange domain being particularly important for the efficiency of the interaction. Using chimeric constructs between XHRT1 and the ESR9 bHLH-O protein that does not interact with Xhairy1 and Xhairy2b, we found that both the bHLH domain and downstream sequences of XHRT1 were required for heterodimerization with Xhairy2b, while only the XHRT1 sequences downstream of the Orange domain are required for the interaction with Xhairy1. Together, these results suggest that XHRT1 plays a role in floor plate cell development and highlight the importance of the Orange and downstream sequences in dimerization and in the selection of the bHLH partners.
XHRT1是HRT/Hey蛋白亚家族的成员,该亚家族被认为是Notch效应器。XHRT1在发育中的底板中表达,并编码一种碱性螺旋-环-螺旋(bHLH)转录抑制因子。在此,我们表明在神经板中XHRT1的错误表达会抑制神经前体细胞的分化,因此对于底板细胞防止其分化为神经元命运可能很重要。缺失分析表明,XHRT1对分化的抑制作用需要DNA结合bHLH基序以及橙色结构域或C末端区域。XHRT1可以与hairy蛋白高效地形成同源二聚体和异源二聚体。在那些hairy基因中,Xhairy2b在底板前体细胞中与XHRT1表现出广泛的表达重叠,可能是与XHRT1具有生物学相关性的伙伴。二聚化是通过bHLH和下游序列介导的,橙色结构域对于相互作用的效率尤为重要。利用XHRT1与不与Xhairy1和Xhairy2b相互作用的ESR9 bHLH-O蛋白之间的嵌合构建体,我们发现XHRT1的bHLH结构域和下游序列对于与Xhairy2b形成异源二聚体都是必需的,而与Xhairy1相互作用仅需要橙色结构域下游的XHRT1序列。总之,这些结果表明XHRT1在底板细胞发育中起作用,并突出了橙色结构域和下游序列在二聚化以及bHLH伙伴选择中的重要性。