Joseph R, Dou D, Tsang W
Department of Neurology, Henry Ford Hospital and Health Sciences Center, Detroit, MI 48202, USA.
Brain Res. 1995 Aug 28;690(1):92-8. doi: 10.1016/0006-8993(95)00621-v.
Neurogenesis begins with the closure of the neural tube around mid gestation and continues in the rat for about two weeks postnatally. Therefore, we investigated the role of neuronatin, a novel cDNA that we cloned from neonatal rat brain (Joseph et al., Biochem. Biophys. Res. Commun., 201 (1994) 1227-1234), in brain development. Further studies described in the present manuscript, lead to the identification of two alternatively spliced forms of neuronatin mRNA, alpha and beta, with the same open reading frame. Neuronatin-alpha encoded a novel protein of 81 aa, and the beta-form encoded 54 aa. Both forms were identical, except that the alpha-form had an additional 81 bp sequence inserted into the middle of the coding region. On Northern analyses, neuronatin mRNA was relatively selective for the brain. It first appeared at E11-14, a time when the neural tube has closed and neuroepithelial proliferation initiated, became pronounced at E16-19 with a surge in neurogenesis, and declined postnatally to adult levels with the completion of neurogenesis. In order to determine whether there were other forms of neuronatin mRNA, and to study the expression of the alpha and beta forms separately during development, reverse transcriptase-polymerase chain reaction was carried out using primers flanking the coding region of the alpha and beta forms. The RT-PCR results clearly indicated that there were only two forms of neuronatin. The beta-form first appeared at E11-14, whereas the alpha-form was present even earlier at E7-10. Together, these findings indicate that the two forms of neuronatin mRNA are regulated differently during brain development.(ABSTRACT TRUNCATED AT 250 WORDS)
神经发生始于妊娠中期左右神经管的闭合,并在出生后的大鼠中持续约两周。因此,我们研究了神经调节蛋白(neuronatin)的作用,它是我们从新生大鼠大脑中克隆的一种新的cDNA(约瑟夫等人,《生物化学与生物物理研究通讯》,201(1994)1227 - 1234),在大脑发育中的作用。本手稿中描述的进一步研究,导致鉴定出神经调节蛋白mRNA的两种选择性剪接形式,α和β,具有相同的开放阅读框。神经调节蛋白-α编码一种81个氨基酸的新蛋白质,β形式编码54个氨基酸。两种形式是相同的,只是α形式在编码区域中间插入了一个额外的81 bp序列。在Northern分析中,神经调节蛋白mRNA对大脑具有相对选择性。它首先出现在E11 - 14,此时神经管已经闭合且神经上皮增殖开始,在E16 - 19随着神经发生的激增而变得明显,并在出生后随着神经发生的完成而下降到成年水平。为了确定是否存在神经调节蛋白mRNA的其他形式,并分别研究α和β形式在发育过程中的表达,使用位于α和β形式编码区域两侧的引物进行逆转录聚合酶链反应。RT-PCR结果清楚地表明神经调节蛋白只有两种形式。β形式首先出现在E11 - 14,而α形式甚至在更早的E7 - 10就已存在。总之,这些发现表明神经调节蛋白mRNA的两种形式在大脑发育过程中受到不同的调节。(摘要截断于250字)