Joseph R, Dou D, Tsang W
Department of Neurology, Laboratory of Molecular Neuroscience Henry Ford Hospital, Detroit, MI.
Biochem Biophys Res Commun. 1994 Jun 30;201(3):1227-34. doi: 10.1006/bbrc.1994.1836.
As differential gene expression governs the progression of development into senescence, we attempted to define the genes that are selectively expressed during postnatal brain development. A cDNA fragment selectively expressed in neonatal rat brain was identified by differential display and used to screen a cDNA library prepared from the same mRNA sample. The full length cDNA, neuronatin, was 1195bp long and coded for a novel protein of 81 amino acids. The cDNA detected an mRNA species of similar size that was highly expressed in rat neonatal and human fetal brain. The deduced protein exhibited a hydrophobic N-terminal and hydrophilic C-terminal, suggesting that it is membrane bound and might function in signal transduction. The selective expression of this novel mRNA in late fetal and early postnatal brain development, and loss of expression in adulthood and senescence, suggests that downregulation of neuronatin may be involved in terminal brain differentiation.
由于差异基因表达控制着从发育到衰老的进程,我们试图确定在出生后脑发育过程中选择性表达的基因。通过差异显示鉴定出在新生大鼠脑中选择性表达的一个cDNA片段,并用于筛选由相同mRNA样品制备的cDNA文库。全长cDNA神经元五肽(neuronatin)长1195bp,编码一种81个氨基酸的新蛋白。该cDNA检测到一种大小相似的mRNA,其在大鼠新生儿和人类胎儿脑中高表达。推导的蛋白质具有疏水的N端和亲水的C端,表明它是膜结合的,可能在信号转导中起作用。这种新mRNA在胎儿后期和出生后早期脑发育中的选择性表达,以及在成年期和衰老期表达的丧失,表明神经元五肽的下调可能参与脑的终末分化。