Cook M, Gould A, Brand N, Davies J, Strutt P, Shaknovich R, Licht J, Waxman S, Chen Z, Gluecksohn-Waelsch S
Laboratory of Developmental Neurobiology, Medical Research Council National Institute for Medical Research, London, United Kingdom.
Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):2249-53. doi: 10.1073/pnas.92.6.2249.
To investigate the potential biological role(s) of the PLZF gene, discovered as a fusion with the RARA locus in a patient with acute promyelocytic leukemia harboring a t(11;17) chromosomal translocation, we have isolated its murine homologue (mPLZF) and studied its patterns of developmental expression. The levels of mPLZF mRNAs increased perinatally in the liver, heart, and kidney, but with the exception of the heart, they were either absent or very low in the adult tissues. In situ analysis of mPLZF expression in mouse embryos between 7.0 and 10.5 days of development revealed that mPLZF mRNAs and proteins were coexpressed in spatially restricted and temporally dynamic patterns in the central nervous system. In the hindbrain region, a segmental pattern of expression correlated with the development of the rhombomeres. From 9.0 days of development, starting first in rhombomeres 3 and 5, there was an ordered down-regulation of expression in the center of each rhombomere, so that 1 day later elevated levels of mPLZF mRNAs and proteins were restricted to cells surrounding the rhombomeric boundaries. The chicken homologue of the PLZF gene, which we have also cloned, demonstrated a similar segmental pattern of expression in the hindbrain. To date, PLZF represents the only example of a transcription factor with elevated expression at rhombomeric boundaries. The high degree of evolutionary conservation between the patterns of PLZF expression during mammalian and avian central nervous system development suggests that it has an important functional role in the regionalization of the vertebrate hindbrain, potentially regulating boundary cell interactions.
为了研究PLZF基因的潜在生物学作用,该基因是在一名患有急性早幼粒细胞白血病且携带t(11;17)染色体易位的患者中作为与RARA基因座融合而被发现的,我们分离了其小鼠同源物(mPLZF)并研究了其发育表达模式。mPLZF mRNA水平在围产期的肝脏、心脏和肾脏中升高,但除心脏外,在成年组织中要么不存在,要么非常低。对发育7.0至10.5天的小鼠胚胎中mPLZF表达的原位分析表明,mPLZF mRNA和蛋白质在中枢神经系统中以空间受限和时间动态的模式共表达。在后脑区域,一种节段性表达模式与菱脑节的发育相关。从发育9.0天开始,首先在菱脑节3和5中,每个菱脑节中心的表达出现有序下调,因此1天后,mPLZF mRNA和蛋白质的升高水平仅限于菱脑节边界周围的细胞。我们也克隆了PLZF基因的鸡同源物,它在后脑显示出类似的节段性表达模式。迄今为止,PLZF是唯一在菱脑节边界表达升高的转录因子的例子。哺乳动物和鸟类中枢神经系统发育过程中PLZF表达模式之间的高度进化保守性表明,它在脊椎动物后脑的区域化中具有重要的功能作用,可能调节边界细胞相互作用。