Saito Yuhki, Miranda-Rottmann Soledad, Ruggiu Matteo, Park Christopher Y, Fak John J, Zhong Ru, Duncan Jeremy S, Fabella Brian A, Junge Harald J, Chen Zhe, Araya Roberto, Fritzsch Bernd, Hudspeth A J, Darnell Robert B
Laboratory of Molecular Neuro-Oncology, Howard Hughes Medical Institute, The Rockefeller University, New York, United States.
New York Genome Center, New York, United States.
Elife. 2016 May 25;5:e14371. doi: 10.7554/eLife.14371.
The neuron specific RNA-binding proteins NOVA1 and NOVA2 are highly homologous alternative splicing regulators. NOVA proteins regulate at least 700 alternative splicing events in vivo, yet relatively little is known about the biologic consequences of NOVA action and in particular about functional differences between NOVA1 and NOVA2. Transcriptome-wide searches for isoform-specific functions, using NOVA1 and NOVA2 specific HITS-CLIP and RNA-seq data from mouse cortex lacking either NOVA isoform, reveals that NOVA2 uniquely regulates alternative splicing events of a series of axon guidance related genes during cortical development. Corresponding axonal pathfinding defects were specific to NOVA2 deficiency: Nova2-/- but not Nova1-/- mice had agenesis of the corpus callosum, and axonal outgrowth defects specific to ventral motoneuron axons and efferent innervation of the cochlea. Thus we have discovered that NOVA2 uniquely regulates alternative splicing of a coordinate set of transcripts encoding key components in cortical, brainstem and spinal axon guidance/outgrowth pathways during neural differentiation, with severe functional consequences in vivo.
神经元特异性RNA结合蛋白NOVA1和NOVA2是高度同源的可变剪接调节因子。NOVA蛋白在体内调节至少700个可变剪接事件,然而,关于NOVA作用的生物学后果,特别是关于NOVA1和NOVA2之间的功能差异,人们了解得相对较少。利用来自缺乏任一NOVA异构体的小鼠皮质的NOVA1和NOVA2特异性HITS-CLIP和RNA-seq数据,在全转录组范围内搜索异构体特异性功能,结果显示,NOVA2在皮质发育过程中独特地调节一系列轴突导向相关基因的可变剪接事件。相应的轴突寻路缺陷是NOVA2缺陷所特有的:Nova2-/-小鼠而非Nova1-/-小鼠有胼胝体发育不全,以及腹侧运动神经元轴突和耳蜗传出神经支配特有的轴突生长缺陷。因此我们发现,NOVA2在神经分化过程中独特地调节一组编码皮质、脑干和脊髓轴突导向/生长途径关键成分的转录本的可变剪接,在体内具有严重的功能后果。