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果蝇 SRPK79D 激酶突变体中的带状轴突聚集物中的 Bruchpilot、行为缺陷和早逝。

Bruchpilot in ribbon-like axonal agglomerates, behavioral defects, and early death in SRPK79D kinase mutants of Drosophila.

机构信息

Department of Genetics and Neurobiology, Julius-Maximilians-University, Würzburg, Germany.

出版信息

PLoS Genet. 2009 Oct;5(10):e1000700. doi: 10.1371/journal.pgen.1000700. Epub 2009 Oct 23.

Abstract

Defining the molecular structure and function of synapses is a central theme in brain research. In Drosophila the Bruchpilot (BRP) protein is associated with T-shaped ribbons ("T-bars") at presynaptic active zones (AZs). BRP is required for intact AZ structure and normal evoked neurotransmitter release. By screening for mutations that affect the tissue distribution of Bruchpilot, we have identified a P-transposon insertion in gene CG11489 (location 79D) which shows high homology to mammalian genes for SR protein kinases (SRPKs). SRPKs phosphorylate serine-arginine rich splicing factors (SR proteins). Since proteins expressed from CG11489 cDNAs phosphorylate a peptide from a human SR protein in vitro, we name CG11489 the Drosophila Srpk79D gene. We have characterized Srpk79D transcripts and generated a null mutant. Mutation of the Srpk79D gene causes conspicuous accumulations of BRP in larval and adult nerves. At the ultrastructural level, these correspond to extensive axonal agglomerates of electron-dense ribbons surrounded by clear vesicles. Basic synaptic structure and function at larval neuromuscular junctions appears normal, whereas life expectancy and locomotor behavior of adult mutants are significantly impaired. All phenotypes of the mutant can be largely or completely rescued by panneural expression of SRPK79D isoforms. Isoform-specific antibodies recognize panneurally overexpressed GFP-tagged SRPK79D-PC isoform co-localized with BRP at presynaptic active zones while the tagged -PB isoform is found in spots within neuronal perikarya. SRPK79D concentrations in wild type apparently are too low to be revealed by these antisera. We propose that the Drosophila Srpk79D gene characterized here may be expressed at low levels throughout the nervous system to prevent the assembly of BRP containing agglomerates in axons and maintain intact brain function. The discovery of an SR protein kinase required for normal BRP distribution calls for the identification of its substrate and the detailed analysis of SRPK function for the maintenance of nervous system integrity.

摘要

定义突触的分子结构和功能是大脑研究的一个核心主题。在果蝇中,Bruchpilot(BRP)蛋白与突触前活性区(AZ)的 T 形带(“T 型条”)相关联。BRP 对于完整的 AZ 结构和正常的诱发神经递质释放是必需的。通过筛选影响 Bruchpilot 组织分布的突变,我们在基因 CG11489(位置 79D)中发现了一个 P-转座子插入,该基因与哺乳动物的 SR 蛋白激酶(SRPKs)高度同源。SRPKs 磷酸化丝氨酸-精氨酸丰富的剪接因子(SR 蛋白)。由于从 CG11489 cDNA 表达的蛋白质在体外磷酸化来自人类 SR 蛋白的肽,因此我们将 CG11489 命名为果蝇 Srpk79D 基因。我们已经对 Srpk79D 转录物进行了表征并生成了一个缺失突变体。Srpk79D 基因的突变导致 BRP 在幼虫和成虫神经中的明显积累。在超微结构水平上,这些对应于电子致密带的广泛轴突聚集物,周围是清晰的小泡。幼虫神经肌肉接头的基本突触结构和功能似乎正常,而成年突变体的预期寿命和运动行为则受到显著损害。突变体的所有表型都可以通过 Srpk79D 同工型的全神经元表达得到很大或完全挽救。同工型特异性抗体识别全神经元过表达的 GFP 标记的 Srpk79D-PC 同工型与 BRP 在突触前活性区共定位,而标记的-PB 同工型则存在于神经元胞体的斑点中。野生型中的 SRPK79D 浓度显然太低,无法通过这些抗血清检测到。我们提出,本文中所描述的果蝇 Srpk79D 基因可能在整个神经系统中以低水平表达,以防止含有 BRP 的聚集物在轴突中组装,并维持完整的大脑功能。发现正常 BRP 分布所需的 SR 蛋白激酶要求鉴定其底物,并详细分析 SRPK 功能以维持神经系统完整性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d31/2759580/b11a103d8e14/pgen.1000700.g001.jpg

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